Skip to main content
Top
Published in: Cancer and Metastasis Reviews 3-4/2011

01-12-2011

Role of lipoxins, resolvins, and other bioactive lipids in colon and pancreatic cancer

Authors: Naveena B. Janakiram, Altaf Mohammed, Chinthalapally V. Rao

Published in: Cancer and Metastasis Reviews | Issue 3-4/2011

Login to get access

Abstract

Unresolved inflammation, due to insufficient production of proresolving anti-inflammatory lipid mediators, can lead to an increased risk of tumorigenesis and tumor cell invasiveness. Various bioactive lipids, particularly those formed by cyclooxygenase (COX) and lipoxygenase (LOX) enzymes, have been well established as therapeutic targets for many epithelial cancers. Emerging studies suggest that there is a role for anti-inflammatory bioactive lipids and their mediators during the resolution phase of inflammation. These proresolving bioactive lipids, including lipoxins (LXs) and resolvins (RVs), have potent anti-inflammatory and anti-carcinogenic properties. The molecular signaling pathways controlling generation and degradation of the proresolving mediators LXs and RVs are now being elucidated, and the component molecules may serve as new targets for regulation of inflammation and inflammation-associated cancers like colon and pancreatic cancers. This review will highlight the recent advances in our understanding of how these bioactive lipids and proresolving mediators may function with various immune cells and cytokines in inhibiting tumor cell proliferation and progression and invasiveness of colon and pancreatic cancers.
Literature
1.
go back to reference Tenesa, A., & Dunlop, M. G. (2009). New insights into the etiology of colorectal cancer from genome-wide association studies. Nature Reviews Genetics, 10, 353–358.PubMed Tenesa, A., & Dunlop, M. G. (2009). New insights into the etiology of colorectal cancer from genome-wide association studies. Nature Reviews Genetics, 10, 353–358.PubMed
2.
go back to reference Jemal, A., Center, M. M., Ward, E., & Thun, M. J. (2009). Cancer occurrence. Methods in Molecular Biology, 471, 3–29.PubMed Jemal, A., Center, M. M., Ward, E., & Thun, M. J. (2009). Cancer occurrence. Methods in Molecular Biology, 471, 3–29.PubMed
3.
go back to reference Jemal, A., Siegel, R., Ward, E., et al. (2008). Cancer statistics. CA: A Cancer Journal for Clinicians, 58, 71–96. Jemal, A., Siegel, R., Ward, E., et al. (2008). Cancer statistics. CA: A Cancer Journal for Clinicians, 58, 71–96.
4.
go back to reference Balkwill, F., & Mantovani, A. (2001). Inflammation and cancer: back to Virchow? Lancet, 357, 539–545.PubMed Balkwill, F., & Mantovani, A. (2001). Inflammation and cancer: back to Virchow? Lancet, 357, 539–545.PubMed
5.
go back to reference Algül, H., Treiber, M., Lesina, M., & Schmid, R. M. (2007). Mechanisms of disease: chronic inflammation and cancer in the pancreas—a potential role for pancreatic stellate cells? Nature Clinical Practice. Gastroenterology & Hepatology, 4, 454–462. Algül, H., Treiber, M., Lesina, M., & Schmid, R. M. (2007). Mechanisms of disease: chronic inflammation and cancer in the pancreas—a potential role for pancreatic stellate cells? Nature Clinical Practice. Gastroenterology & Hepatology, 4, 454–462.
6.
go back to reference Whitcomb, D. C., Gorry, M. C., Preston, R. A., Furey, W., Sossenheimer, M. J., Ulrich, C. D., et al. (1996). Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene. Nature Genetics, 14, 141–145.PubMed Whitcomb, D. C., Gorry, M. C., Preston, R. A., Furey, W., Sossenheimer, M. J., Ulrich, C. D., et al. (1996). Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene. Nature Genetics, 14, 141–145.PubMed
7.
go back to reference Hruban, R. H., Wilentz, R. E., & Kern, S. E. (2000). Genetic progression in the pancreatic ducts. American Journal of Pathology, 156, 1821–1825.PubMed Hruban, R. H., Wilentz, R. E., & Kern, S. E. (2000). Genetic progression in the pancreatic ducts. American Journal of Pathology, 156, 1821–1825.PubMed
8.
go back to reference Raimondi, S., Maisonneuve, P., & Lowenfels, A. B. (2009). Epidemiology of pancreatic cancer: an overview. Nature Reviews. Gastroenterology & Hepatology, 6, 699–708. Raimondi, S., Maisonneuve, P., & Lowenfels, A. B. (2009). Epidemiology of pancreatic cancer: an overview. Nature Reviews. Gastroenterology & Hepatology, 6, 699–708.
9.
go back to reference Greer, J. B., & Whitcomb, D. C. (2009). Inflammation and pancreatic cancer: an evidence-based review. Current Opinion in Pharmacology, 9, 411–418.PubMed Greer, J. B., & Whitcomb, D. C. (2009). Inflammation and pancreatic cancer: an evidence-based review. Current Opinion in Pharmacology, 9, 411–418.PubMed
10.
go back to reference Serhan, C. N. (1997). Lipoxins and novel aspirin-triggered 15-epi-lipoxins (ATL). Prostaglandins, 53, 107–137.PubMed Serhan, C. N. (1997). Lipoxins and novel aspirin-triggered 15-epi-lipoxins (ATL). Prostaglandins, 53, 107–137.PubMed
11.
go back to reference Maitra, A., Ashfaq, R., Gunn, C. R., Rahman, A., Yeo, C. J., Sohn, T. A., et al. (2002). Cyclooxygenase-2 expression in pancreatic adenocarcinoma and pancreatic intraepithelial neoplasia: an immunohistochemical analysis with automated cellular imaging. American Journal of Clinical Pathology, 118, 194–201.PubMed Maitra, A., Ashfaq, R., Gunn, C. R., Rahman, A., Yeo, C. J., Sohn, T. A., et al. (2002). Cyclooxygenase-2 expression in pancreatic adenocarcinoma and pancreatic intraepithelial neoplasia: an immunohistochemical analysis with automated cellular imaging. American Journal of Clinical Pathology, 118, 194–201.PubMed
12.
go back to reference Rao, C. V., & Reddy, B. S. (2004). NSAIDs and chemoprevention. Current Cancer Drug Targets, 4, 29–42.PubMed Rao, C. V., & Reddy, B. S. (2004). NSAIDs and chemoprevention. Current Cancer Drug Targets, 4, 29–42.PubMed
13.
go back to reference Castellone, M. D., Teramoto, H., & Gutkind, J. S. (2006). Cyclooxygenase-2 and colorectal cancer chemoprevention: the beta-catenin connection. Cancer Research, 66, 11085–11088.PubMed Castellone, M. D., Teramoto, H., & Gutkind, J. S. (2006). Cyclooxygenase-2 and colorectal cancer chemoprevention: the beta-catenin connection. Cancer Research, 66, 11085–11088.PubMed
14.
go back to reference Dorsam, R. T., & Gutkind, J. S. (2007). G-protein-coupled receptors and cancer. Nature Reviews. Cancer, 7, 79–94.PubMed Dorsam, R. T., & Gutkind, J. S. (2007). G-protein-coupled receptors and cancer. Nature Reviews. Cancer, 7, 79–94.PubMed
15.
go back to reference Cherukuri, D. P., Chen, X. B. O., Goulet, A., et al. (2007). The EP4 receptor antagonist, L-161,982, blocks prostaglandin E2-induced signal transduction and cell proliferation in HCA-7 colon cancer cells. Experimental Cell Research, 313, 2969–2979.PubMed Cherukuri, D. P., Chen, X. B. O., Goulet, A., et al. (2007). The EP4 receptor antagonist, L-161,982, blocks prostaglandin E2-induced signal transduction and cell proliferation in HCA-7 colon cancer cells. Experimental Cell Research, 313, 2969–2979.PubMed
16.
go back to reference Murata, T., Lin, M. I., Aritake, K., et al. (2008). Role of prostaglandin D2 receptor DP as a suppressor of tumor hyperpermeability and angiogenesis in vivo. Proceedings of the National Academy of Sciences, 105(50), 20009–20014. Murata, T., Lin, M. I., Aritake, K., et al. (2008). Role of prostaglandin D2 receptor DP as a suppressor of tumor hyperpermeability and angiogenesis in vivo. Proceedings of the National Academy of Sciences, 105(50), 20009–20014.
17.
go back to reference Backlund, M. G., Mann, J. R., Holla, V. R., et al. (2005). 15-Hydroxyprostaglandin dehydrogenase is down-regulated in colorectal cancer. Journal of Biological Chemistry, 280(5), 3217–3223.PubMed Backlund, M. G., Mann, J. R., Holla, V. R., et al. (2005). 15-Hydroxyprostaglandin dehydrogenase is down-regulated in colorectal cancer. Journal of Biological Chemistry, 280(5), 3217–3223.PubMed
18.
go back to reference Molina, M. A., Sitja-Amau, M., Lemoine, M. G., Frazier, M., & Sinicrope, F. A. (1999). Increased cyclooxygenase-2 expression in human pancreatic carcinomas and cell lines: growth inhibition by nonsteroidal anti-inflammatory drugs. Cancer Research, 59, 4356–4362.PubMed Molina, M. A., Sitja-Amau, M., Lemoine, M. G., Frazier, M., & Sinicrope, F. A. (1999). Increased cyclooxygenase-2 expression in human pancreatic carcinomas and cell lines: growth inhibition by nonsteroidal anti-inflammatory drugs. Cancer Research, 59, 4356–4362.PubMed
19.
go back to reference Okami, J., Yamamoto, H., Fujiwara, Y., Tsujie, M., Kondo, K., Noura, S., et al. (1999). Overexpression of cyclooxygenase-2 in carcinoma of the pancreas. Clinical Cancer Research, 5, 2018–2024.PubMed Okami, J., Yamamoto, H., Fujiwara, Y., Tsujie, M., Kondo, K., Noura, S., et al. (1999). Overexpression of cyclooxygenase-2 in carcinoma of the pancreas. Clinical Cancer Research, 5, 2018–2024.PubMed
20.
go back to reference Tucker, O. N., Dannenberg, A. J., Yang, E. K., Zhang, F., Teng, L., Daly, J. M., et al. (1999). Cyclooxygenase-2 expression is up-regulated in human pancreatic cancer. Cancer Research, 59, 987–990.PubMed Tucker, O. N., Dannenberg, A. J., Yang, E. K., Zhang, F., Teng, L., Daly, J. M., et al. (1999). Cyclooxygenase-2 expression is up-regulated in human pancreatic cancer. Cancer Research, 59, 987–990.PubMed
21.
go back to reference Niijima, M., Yamaguchi, T., Ishihara, T., et al. (2002). Immunohistochemical analysis and in situ hybridization of cyclooxygenase-2 expression in intraductal papillary-mucinous tumors of the pancreas. Cancer, 94, 1565–1573.PubMed Niijima, M., Yamaguchi, T., Ishihara, T., et al. (2002). Immunohistochemical analysis and in situ hybridization of cyclooxygenase-2 expression in intraductal papillary-mucinous tumors of the pancreas. Cancer, 94, 1565–1573.PubMed
22.
go back to reference Bergmann, F., Breinig, M., Hopfner, M., et al. (2009). Expression pattern and functional relevance of epidermal growth factor receptor and cyclooxygenase-2: novel chemotherapeutic targets in pancreatic endocrine tumors? American Journal of Gastroenterology, 104, 171–181.PubMed Bergmann, F., Breinig, M., Hopfner, M., et al. (2009). Expression pattern and functional relevance of epidermal growth factor receptor and cyclooxygenase-2: novel chemotherapeutic targets in pancreatic endocrine tumors? American Journal of Gastroenterology, 104, 171–181.PubMed
23.
go back to reference Hermanova, M., Karasek, P., Nenutil, R., et al. (2009). Clinicopathological correlations of cyclooxygenase-2, MDM2, and p53 expressions in surgically resectable pancreatic invasive ductal adenocarcinoma. Pancreas, 38, 565–571.PubMed Hermanova, M., Karasek, P., Nenutil, R., et al. (2009). Clinicopathological correlations of cyclooxygenase-2, MDM2, and p53 expressions in surgically resectable pancreatic invasive ductal adenocarcinoma. Pancreas, 38, 565–571.PubMed
24.
go back to reference Levitt, R. J., & Pollak, M. (2002). Insulin-like growth factor-I antagonizes the antiproliferative effects of cyclooxygenase-2 inhibitors on BxPC-3 pancreatic cancer cells. Cancer Research, 62, 7372–7376.PubMed Levitt, R. J., & Pollak, M. (2002). Insulin-like growth factor-I antagonizes the antiproliferative effects of cyclooxygenase-2 inhibitors on BxPC-3 pancreatic cancer cells. Cancer Research, 62, 7372–7376.PubMed
25.
go back to reference Pold, M., Krysan, K., Pold, A., Dohadwala, M., Heuze-Vourc’h, N., Mao, J. T., et al. (2004). Cyclooxygenase-2 modulates the insulin-like growth factor axis in non-small-cell lung cancer. Cancer Research, 64, 6549–6555.PubMed Pold, M., Krysan, K., Pold, A., Dohadwala, M., Heuze-Vourc’h, N., Mao, J. T., et al. (2004). Cyclooxygenase-2 modulates the insulin-like growth factor axis in non-small-cell lung cancer. Cancer Research, 64, 6549–6555.PubMed
26.
go back to reference Stoeltzing, O., Liu, W., Fan, F., Wagner, C., Stengel, K., Somcio, J. R., et al. (2007). Regulation of cyclooxygenase-2 (COX-2) expression in human pancreatic carcinoma cells by the insulin-like growth factor-I receptor (IGF-IR) system. Cancer Letters, 258(2), 291–300.PubMed Stoeltzing, O., Liu, W., Fan, F., Wagner, C., Stengel, K., Somcio, J. R., et al. (2007). Regulation of cyclooxygenase-2 (COX-2) expression in human pancreatic carcinoma cells by the insulin-like growth factor-I receptor (IGF-IR) system. Cancer Letters, 258(2), 291–300.PubMed
27.
go back to reference Rao, C.V., Mohammed, A., Janakiram, N., Qian, L., Choi, C., Zhang, Y., Lightfoot, Stan., Steele, V.E. (2009). Delayed progression of pancreatic carcinoma in a conditional K-rasG12D mice by nitric oxide (NO)-releasing aspirin. In 100 th AACR annual meeting, Apr; #2062. Rao, C.V., Mohammed, A., Janakiram, N., Qian, L., Choi, C., Zhang, Y., Lightfoot, Stan., Steele, V.E. (2009). Delayed progression of pancreatic carcinoma in a conditional K-rasG12D mice by nitric oxide (NO)-releasing aspirin. In 100 th AACR annual meeting, Apr; #2062.
28.
go back to reference Tong, W. G., Ding, X. Z., Hennig, R., Witt, R. C., Standop, J., Pour, P. M., et al. (2002). Leukotriene B4 receptor antagonist LY293111 inhibits proliferation and induces apoptosis in human pancreatic cancer cells. Clinical Cancer Research, 8, 3232–3242.PubMed Tong, W. G., Ding, X. Z., Hennig, R., Witt, R. C., Standop, J., Pour, P. M., et al. (2002). Leukotriene B4 receptor antagonist LY293111 inhibits proliferation and induces apoptosis in human pancreatic cancer cells. Clinical Cancer Research, 8, 3232–3242.PubMed
29.
go back to reference Ohd, J. F., Nielsen, C. K., Campbell, J., Landberg, G., Lofberg, H., & Sjolander, A. (2003). Expression of the leukotriene D4 receptor CysLT1, COX-2, and other cell survival factors in colorectal adenocarcinomas. Gastroenterology, 124, 57–70.PubMed Ohd, J. F., Nielsen, C. K., Campbell, J., Landberg, G., Lofberg, H., & Sjolander, A. (2003). Expression of the leukotriene D4 receptor CysLT1, COX-2, and other cell survival factors in colorectal adenocarcinomas. Gastroenterology, 124, 57–70.PubMed
30.
go back to reference Hayashi, T., Nishiyama, K., & Shirahama, T. (2006). Inhibition of 5-lipoxygenase pathway suppresses the growth of bladder cancer cells. International Journal of Urology, 13, 1086–1091.PubMed Hayashi, T., Nishiyama, K., & Shirahama, T. (2006). Inhibition of 5-lipoxygenase pathway suppresses the growth of bladder cancer cells. International Journal of Urology, 13, 1086–1091.PubMed
31.
go back to reference Zhi, H., Zhang, J., Hu, G., Lu, J., Wang, X., Zhou, C., et al. (2003). The deregulation of arachidonic acid metabolism-related genes in human esophageal squamous cell carcinoma. International Journal of Cancer, 106, 327–333. Zhi, H., Zhang, J., Hu, G., Lu, J., Wang, X., Zhou, C., et al. (2003). The deregulation of arachidonic acid metabolism-related genes in human esophageal squamous cell carcinoma. International Journal of Cancer, 106, 327–333.
32.
go back to reference Yoshimura, R., Matsuyama, M., Tsuchida, K., Kawahito, Y., Sano, H., & Nakatani, T. (2003). Expression of lipoxygenase in human bladder carcinoma and growth inhibition by its inhibitors. Journal of Urology, 170, 1994–1999.PubMed Yoshimura, R., Matsuyama, M., Tsuchida, K., Kawahito, Y., Sano, H., & Nakatani, T. (2003). Expression of lipoxygenase in human bladder carcinoma and growth inhibition by its inhibitors. Journal of Urology, 170, 1994–1999.PubMed
33.
go back to reference Qiao, L., Kozoni, V., Tsioulias, G. J., Koutsos, M. I., Hanif, R., Shiff, S. J., et al. (1995). Selected eicosanoids increase the proliferation rate of human colon carcinoma cell lines and mouse colonocytes in vivo. Biochimica et Biophysical Acta, 1258, 215–223. Qiao, L., Kozoni, V., Tsioulias, G. J., Koutsos, M. I., Hanif, R., Shiff, S. J., et al. (1995). Selected eicosanoids increase the proliferation rate of human colon carcinoma cell lines and mouse colonocytes in vivo. Biochimica et Biophysical Acta, 1258, 215–223.
34.
go back to reference Bortuzzo, C., Hanif, R., Kashfi, K., Staiano-Coico, L., Shiff, S. J., Rigas, B., et al. (1996). The effect of leukotrienes B and selected HETEs on the proliferation of colon cancer cells. Biochimica et Biophysical Acta, 1300, 240–246. Bortuzzo, C., Hanif, R., Kashfi, K., Staiano-Coico, L., Shiff, S. J., Rigas, B., et al. (1996). The effect of leukotrienes B and selected HETEs on the proliferation of colon cancer cells. Biochimica et Biophysical Acta, 1300, 240–246.
35.
go back to reference Avis, I., Hong, S. H., Martinez, A., Moody, T., Choi, Y. H., Trepel, J., et al. (2001). Five-lipoxygenase inhibitors can mediate apoptosis in human breast cancer cell lines through complex eicosanoid interactions. Journal of the Federation of American Societies for Experimental Biology, 15, 2007–2009. Avis, I., Hong, S. H., Martinez, A., Moody, T., Choi, Y. H., Trepel, J., et al. (2001). Five-lipoxygenase inhibitors can mediate apoptosis in human breast cancer cell lines through complex eicosanoid interactions. Journal of the Federation of American Societies for Experimental Biology, 15, 2007–2009.
36.
go back to reference Ding, X. Z., Tong, W. G., & Adrian, T. E. (2003). Multiple signal pathways are involved in the mitogenic effect of 5(S)-HETE in human pancreatic cancer. Oncology, 65, 285–294.PubMed Ding, X. Z., Tong, W. G., & Adrian, T. E. (2003). Multiple signal pathways are involved in the mitogenic effect of 5(S)-HETE in human pancreatic cancer. Oncology, 65, 285–294.PubMed
37.
go back to reference Tong, W. G., Ding, X. Z., Talamonti, M. S., Bell, R. H., & Adrian, T. E. (2005). LTB4 stimulates growth of human pancreatic cancer cells via MAPK and PI-3 kinase pathways. Biochemical Biophysical Research Communication, 335, 949–956. Tong, W. G., Ding, X. Z., Talamonti, M. S., Bell, R. H., & Adrian, T. E. (2005). LTB4 stimulates growth of human pancreatic cancer cells via MAPK and PI-3 kinase pathways. Biochemical Biophysical Research Communication, 335, 949–956.
38.
go back to reference Hong, S. H., Avis, I., Vos, M. D., Martinez, A., Treston, A. M., & Mulshine, J. L. (1999). Relationship of arachidonic acid metabolizing enzyme expression in epithelial cancer cell lines to the growth effect of selective biochemical inhibitors. Cancer Research, 59, 2223–2228.PubMed Hong, S. H., Avis, I., Vos, M. D., Martinez, A., Treston, A. M., & Mulshine, J. L. (1999). Relationship of arachidonic acid metabolizing enzyme expression in epithelial cancer cell lines to the growth effect of selective biochemical inhibitors. Cancer Research, 59, 2223–2228.PubMed
39.
go back to reference Hennig, R., Ding, X. Z., Tong, W. G., Schneider, M. B., Standop, J., Friess, H., et al. (2002). 5-Lipoxygenase and leukotriene B(4) receptor are expressed in human pancreatic cancers but not in pancreatic ducts in normal tissue. American Journal of Pathology, 161, 421–428.PubMed Hennig, R., Ding, X. Z., Tong, W. G., Schneider, M. B., Standop, J., Friess, H., et al. (2002). 5-Lipoxygenase and leukotriene B(4) receptor are expressed in human pancreatic cancers but not in pancreatic ducts in normal tissue. American Journal of Pathology, 161, 421–428.PubMed
40.
go back to reference Ding, X. Z., Talamonti, M. S., Bell, R. H., Jr., & Adrian, T. E. (2005). A novel anti-pancreatic cancer agent, LY293111. Anti-Cancer Drugs, 16, 467–473.PubMed Ding, X. Z., Talamonti, M. S., Bell, R. H., Jr., & Adrian, T. E. (2005). A novel anti-pancreatic cancer agent, LY293111. Anti-Cancer Drugs, 16, 467–473.PubMed
41.
go back to reference Tong, W. G., Ding, X. Z., Talamonti, M. S., Bell, R. H., & Adrian, T. E. (2007). Leukotriene B4 receptor antagonist LY293111 induces S-phase cell cycle arrest and apoptosis in human pancreatic cancer cells. Anti-Cancer Drugs, 18, 535–541.PubMed Tong, W. G., Ding, X. Z., Talamonti, M. S., Bell, R. H., & Adrian, T. E. (2007). Leukotriene B4 receptor antagonist LY293111 induces S-phase cell cycle arrest and apoptosis in human pancreatic cancer cells. Anti-Cancer Drugs, 18, 535–541.PubMed
42.
go back to reference Edderkaoui, M., Hong, P., Vaquero, E. C., Lee, J. K., Fischer, L., Friess, H., et al. (2005). Extracellular matrix stimulates reactive oxygen species production and increases pancreatic cancer cell survival through 5-lipoxygenase and NADPH oxidase. American Journal of Physiology—Gastrointestinal and Liver Physiology, 289, G1137–G1147.PubMed Edderkaoui, M., Hong, P., Vaquero, E. C., Lee, J. K., Fischer, L., Friess, H., et al. (2005). Extracellular matrix stimulates reactive oxygen species production and increases pancreatic cancer cell survival through 5-lipoxygenase and NADPH oxidase. American Journal of Physiology—Gastrointestinal and Liver Physiology, 289, G1137–G1147.PubMed
43.
go back to reference Melstrom, L. G., Bentrem, D. J., Salabat, M. R., Kennedy, T. J., Ding, X. Z., Strouch, M., et al. (2008). Overexpression of 5-lipoxygenase in colon polyps and cancer and the effect of 5-LOX inhibitors in vitro and in a murine model. Clinical Cancer Research, 14, 6525–6530.PubMed Melstrom, L. G., Bentrem, D. J., Salabat, M. R., Kennedy, T. J., Ding, X. Z., Strouch, M., et al. (2008). Overexpression of 5-lipoxygenase in colon polyps and cancer and the effect of 5-LOX inhibitors in vitro and in a murine model. Clinical Cancer Research, 14, 6525–6530.PubMed
44.
go back to reference Saif, M. W., Oettle, H., Vervenne, W. L., Thomas, J. P., Spitzer, G., Visseren-Grul, C., et al. (2009). Randomized double-blind phase II trial comparing gemcitabine plus LY293111 versus gemcitabine plus placebo in advanced adenocarcinoma of the pancreas. Cancer Journal of Clinicians, 15, 339–343. Saif, M. W., Oettle, H., Vervenne, W. L., Thomas, J. P., Spitzer, G., Visseren-Grul, C., et al. (2009). Randomized double-blind phase II trial comparing gemcitabine plus LY293111 versus gemcitabine plus placebo in advanced adenocarcinoma of the pancreas. Cancer Journal of Clinicians, 15, 339–343.
45.
go back to reference Romano, M., & Claria, J. (2003). Cyclooxygenase-2 and 5-lipoxygenase converging functions on cell proliferation and tumor angiogenesis: implications for cancer therapy. Federation of American Society for Experimental Biology, 17, 1986–1995. Romano, M., & Claria, J. (2003). Cyclooxygenase-2 and 5-lipoxygenase converging functions on cell proliferation and tumor angiogenesis: implications for cancer therapy. Federation of American Society for Experimental Biology, 17, 1986–1995.
46.
go back to reference Byrum, R. S., Goulet, J. L., Griffiths, R. J., & Koller, B. H. (1997). Role of the 5-lipoxygenase-activating protein (FLAP) in murine acute inflammatory responses. The Journal of Experimental Medicine, 185, 1065–1075.PubMed Byrum, R. S., Goulet, J. L., Griffiths, R. J., & Koller, B. H. (1997). Role of the 5-lipoxygenase-activating protein (FLAP) in murine acute inflammatory responses. The Journal of Experimental Medicine, 185, 1065–1075.PubMed
47.
go back to reference Griffiths, R. J., Smith, M. A., Roach, M. L., Stock, J. L., Stam, E. J., Milici, A. J., et al. (1997). Collagen-induced arthritis is reduced in 5-lipoxygenase-activating protein-deficient mice. The Journal of Experimental Medicine, 185, 1123–1129.PubMed Griffiths, R. J., Smith, M. A., Roach, M. L., Stock, J. L., Stam, E. J., Milici, A. J., et al. (1997). Collagen-induced arthritis is reduced in 5-lipoxygenase-activating protein-deficient mice. The Journal of Experimental Medicine, 185, 1123–1129.PubMed
48.
go back to reference Goulet, J. L., Snouwaert, J. N., Latour, A. M., Coffman, T. M., & Koller, B. H. (1994). Altered inflammatory responses in leukotriene-deficient mice. Proceedings of the National Academy of Sciences, 91, 12852–12856. Goulet, J. L., Snouwaert, J. N., Latour, A. M., Coffman, T. M., & Koller, B. H. (1994). Altered inflammatory responses in leukotriene-deficient mice. Proceedings of the National Academy of Sciences, 91, 12852–12856.
49.
go back to reference Peters-Golden, M., Bailie, M., Marshall, T., Wilke, C., Phan, S. H., Toews, G. B., et al. (2002). Protection from pulmonary fibrosis in leukotriene-deficient mice. American Journal of Respiratory and Critical Care Medicine, 165, 229–235.PubMed Peters-Golden, M., Bailie, M., Marshall, T., Wilke, C., Phan, S. H., Toews, G. B., et al. (2002). Protection from pulmonary fibrosis in leukotriene-deficient mice. American Journal of Respiratory and Critical Care Medicine, 165, 229–235.PubMed
50.
go back to reference Gavett, S. H., Madison, S. L., Chulada, P. C., Scarborough, P. E., Qu, W., Boyle, J. E., et al. (1999). Allergic lung responses are increased in prostaglandin H synthase-deficient mice. Journal of Clinical Investigation, 104, 721–732.PubMed Gavett, S. H., Madison, S. L., Chulada, P. C., Scarborough, P. E., Qu, W., Boyle, J. E., et al. (1999). Allergic lung responses are increased in prostaglandin H synthase-deficient mice. Journal of Clinical Investigation, 104, 721–732.PubMed
51.
go back to reference Celotti, F., & Durand, T. (2003). The metabolic effects of inhibitors of 5-lipoxygenase and of cyclooxygenase 1 and 2 are an advancement in the efficacy and safety of anti-inflammatory therapy. Prostaglandins & Other Lipid Mediators, 71, 147–162. Celotti, F., & Durand, T. (2003). The metabolic effects of inhibitors of 5-lipoxygenase and of cyclooxygenase 1 and 2 are an advancement in the efficacy and safety of anti-inflammatory therapy. Prostaglandins & Other Lipid Mediators, 71, 147–162.
52.
go back to reference Fiorucci, S., Meli, R., Bucci, M., & Cirino, G. (2001). Dual inhibitors of cyclooxygenase and 5-lipoxygenase. A new avenue in anti-inflammatory therapy? Biochemical Pharmacology, 62, 1433–1438.PubMed Fiorucci, S., Meli, R., Bucci, M., & Cirino, G. (2001). Dual inhibitors of cyclooxygenase and 5-lipoxygenase. A new avenue in anti-inflammatory therapy? Biochemical Pharmacology, 62, 1433–1438.PubMed
53.
go back to reference Ding, X. Z., Iversen, P., Cluck, M. W., Knezetic, J. A., & Adrian, T. E. (1999). Lipoxygenase inhibitors abolish proliferation of human pancreatic cancer cells. Biochemical and Biophysical Research Communications, 261, 218–223.PubMed Ding, X. Z., Iversen, P., Cluck, M. W., Knezetic, J. A., & Adrian, T. E. (1999). Lipoxygenase inhibitors abolish proliferation of human pancreatic cancer cells. Biochemical and Biophysical Research Communications, 261, 218–223.PubMed
54.
go back to reference Ding, X. Z., Tong, W. G., & Adrian, T. E. (2001). 12-Lipoxygenase metabolite 12(S)-HETE stimulates human pancreatic cancer cell proliferation via protein tyrosine phosphorylation and ERK activation. International Journal of Cancer, 94, 630–636. Ding, X. Z., Tong, W. G., & Adrian, T. E. (2001). 12-Lipoxygenase metabolite 12(S)-HETE stimulates human pancreatic cancer cell proliferation via protein tyrosine phosphorylation and ERK activation. International Journal of Cancer, 94, 630–636.
55.
go back to reference Mohammed, A., Qian, L., Janakiram, N., Choi, C., Zhang, Y., Steele, V.E. Rao, C.V., (2009). Chemoprevention of colon and small intestinal tumorigenesis in ApcMin/+ mice by licofelone, a novel dual 5-LOX/COX inhibitor. In 100 th AACR annual meeting, Apr; #4781. Mohammed, A., Qian, L., Janakiram, N., Choi, C., Zhang, Y., Steele, V.E. Rao, C.V., (2009). Chemoprevention of colon and small intestinal tumorigenesis in ApcMin/+ mice by licofelone, a novel dual 5-LOX/COX inhibitor. In 100 th AACR annual meeting, Apr; #4781.
56.
go back to reference Mohammed, A., Janakiram, N., Ely, M., Lightfoot, Stan., Steele, V.E. Rao, C.V., (2011). Licofelone, a novel dual COX–LOX inhibitor prevents progression of panIN lesions to pancreatic carcinoma by targeting miRNAs and cancer stem cells in p48 Cre/+-LSL-Kras G12D transgenic mice. In 102 nd AACR annual meeting, Apr 2–6; #2839. Mohammed, A., Janakiram, N., Ely, M., Lightfoot, Stan., Steele, V.E. Rao, C.V., (2011). Licofelone, a novel dual COX–LOX inhibitor prevents progression of panIN lesions to pancreatic carcinoma by targeting miRNAs and cancer stem cells in p48 Cre/+-LSL-Kras G12D transgenic mice. In 102 nd AACR annual meeting, Apr 2–6; #2839.
57.
go back to reference Alvaro-Gracia, J. M. (2004). Licofelone—clinical update on a novel LOX/COX inhibitor for the treatment of osteoarthritis. Rheumatology (Oxford, England), 43(Suppl 1), i21–i25. Alvaro-Gracia, J. M. (2004). Licofelone—clinical update on a novel LOX/COX inhibitor for the treatment of osteoarthritis. Rheumatology (Oxford, England), 43(Suppl 1), i21–i25.
58.
go back to reference Chiang, N., Arita, M., & Serhan, C. N. (2005). Anti-inflammatory circuitry: lipoxin, aspirin-triggered lipoxins and their receptor ALX. Prostaglandins, Leukotrienes, and Essential Fatty Acids, 73, 163–177.PubMed Chiang, N., Arita, M., & Serhan, C. N. (2005). Anti-inflammatory circuitry: lipoxin, aspirin-triggered lipoxins and their receptor ALX. Prostaglandins, Leukotrienes, and Essential Fatty Acids, 73, 163–177.PubMed
59.
go back to reference Brezinski, M. E., & Serhan, C. N. (1990). Selective incorporation of (15S)-hydroxyeicosatetraenoic acid in phosphatidylinositol of human neutrophils: agonist-induced deacylation and transformation of stored hydroxyeicosanoids. Proceedings of the National Academy of Sciences, 87, 6248–6252. Brezinski, M. E., & Serhan, C. N. (1990). Selective incorporation of (15S)-hydroxyeicosatetraenoic acid in phosphatidylinositol of human neutrophils: agonist-induced deacylation and transformation of stored hydroxyeicosanoids. Proceedings of the National Academy of Sciences, 87, 6248–6252.
60.
go back to reference Claria, J., & Serhan, C. N. (1995). Aspirin triggers previously undescribed bioactive eicosanoids by human endothelial cell–leukocyte interactions. Proceedings of the National Academy of Sciences, 92, 9475–9479. Claria, J., & Serhan, C. N. (1995). Aspirin triggers previously undescribed bioactive eicosanoids by human endothelial cell–leukocyte interactions. Proceedings of the National Academy of Sciences, 92, 9475–9479.
61.
go back to reference Kieran, N. E., Maderna, P., & Godson, C. (2004). Lipoxins: potential anti-inflammatory, proresolution, and antifibrotic mediators in renal disease. Kidney International, 65, 1145–1154.PubMed Kieran, N. E., Maderna, P., & Godson, C. (2004). Lipoxins: potential anti-inflammatory, proresolution, and antifibrotic mediators in renal disease. Kidney International, 65, 1145–1154.PubMed
62.
go back to reference Serhan, C. N. (2002). Lipoxins and aspirin-triggered 15-epi-lipoxin biosynthesis: an update and role in anti-inflammation and pro-resolution. Prostaglandins Other Lipid mediators, 68–69, 4333–4455. Serhan, C. N. (2002). Lipoxins and aspirin-triggered 15-epi-lipoxin biosynthesis: an update and role in anti-inflammation and pro-resolution. Prostaglandins Other Lipid mediators, 68–69, 4333–4455.
63.
go back to reference Canny, G., Levy, O., Furuta, G. T., Narravula-Alipati, S., Sisson, R. B., Serhan, C. N., et al. (2002). Lipid mediator-induced expression of bactericidal/permeability-increasing protein (BPI) in human mucosal epithelia. Proceedings of the National Academy of Sciences, 99, 3902–3907. Canny, G., Levy, O., Furuta, G. T., Narravula-Alipati, S., Sisson, R. B., Serhan, C. N., et al. (2002). Lipid mediator-induced expression of bactericidal/permeability-increasing protein (BPI) in human mucosal epithelia. Proceedings of the National Academy of Sciences, 99, 3902–3907.
64.
go back to reference Serhan, C. N., Maddox, J. F., Petasis, N. A., Akritopoulou-Zanze, I., Papayianni, A., Brady, H. R., et al. (1995). Design of lipoxin A4 stable analogs that block transmigration and adhesion of human neutrophils. Biochemistry, 34(44), 14609–14615.PubMed Serhan, C. N., Maddox, J. F., Petasis, N. A., Akritopoulou-Zanze, I., Papayianni, A., Brady, H. R., et al. (1995). Design of lipoxin A4 stable analogs that block transmigration and adhesion of human neutrophils. Biochemistry, 34(44), 14609–14615.PubMed
65.
go back to reference Aliberti, J., Hieny, S., Reise, S. C., Serhan, C. N., & Sher, A. (2002). Lipoxin-mediated inhibition of interleukin-12 production by dendritic cells: a mechanism for the regulation of microbial immunity. Nature Immunology, 3, 76–82.PubMed Aliberti, J., Hieny, S., Reise, S. C., Serhan, C. N., & Sher, A. (2002). Lipoxin-mediated inhibition of interleukin-12 production by dendritic cells: a mechanism for the regulation of microbial immunity. Nature Immunology, 3, 76–82.PubMed
66.
go back to reference Fierro, I. M., Colgan, S. P., Bernasconi, G., Petasis, N. A., Clish, C. B., Arita, M., et al. (2003). Lipoxin A4 and aspirin-triggered 15-epi-lipoxin A4 inhibit human neutrophil migration: comparisons between synthetic 15 epimers in chemotaxis and transmigration with microvessel endothelial cells and epithelial cells. Journal of Immunology, 170, 2688–2694. Fierro, I. M., Colgan, S. P., Bernasconi, G., Petasis, N. A., Clish, C. B., Arita, M., et al. (2003). Lipoxin A4 and aspirin-triggered 15-epi-lipoxin A4 inhibit human neutrophil migration: comparisons between synthetic 15 epimers in chemotaxis and transmigration with microvessel endothelial cells and epithelial cells. Journal of Immunology, 170, 2688–2694.
67.
go back to reference Zhou, M., Chen, B., Sun, H., Deng, Z., Andersson, R., & Zhang, Q. (2011). The protective effects of lipoxin A4 during the early phase of severe acute pancreatitis in rats. Scandinavian Journal of gasteroenterology, 46(2), 211–219. Zhou, M., Chen, B., Sun, H., Deng, Z., Andersson, R., & Zhang, Q. (2011). The protective effects of lipoxin A4 during the early phase of severe acute pancreatitis in rats. Scandinavian Journal of gasteroenterology, 46(2), 211–219.
68.
go back to reference Songjun, L., Ping, W., Duyun, Y., Yinping, H., Xiaoyan, Z., Yongsheng, L., et al. (2009). Effects of lipoxin A4 on CoCl2-induced angiogenesis and its possible mechanisms in human umbilical vein endothelial cells. Pharmacology, 84, 17–23. Songjun, L., Ping, W., Duyun, Y., Yinping, H., Xiaoyan, Z., Yongsheng, L., et al. (2009). Effects of lipoxin A4 on CoCl2-induced angiogenesis and its possible mechanisms in human umbilical vein endothelial cells. Pharmacology, 84, 17–23.
69.
go back to reference Bellenger, J., Bellenger, S., Bataille, A., Massey, K. A., Nicolaou, A., Rialland, M., et al. (2010). High pancreatic n-3 fatty acids prevent STZ-induced diabetes in fat-1 mice: inflammatory pathway inhibition. Diabetes, 60, 1090–1099. Bellenger, J., Bellenger, S., Bataille, A., Massey, K. A., Nicolaou, A., Rialland, M., et al. (2010). High pancreatic n-3 fatty acids prevent STZ-induced diabetes in fat-1 mice: inflammatory pathway inhibition. Diabetes, 60, 1090–1099.
70.
go back to reference Cezar-de-Mello, P. F. T., Vieira, A. M., Nascimento-Silva, V., Villela, C. G., Barja-Fidalgo, C., & Fierro, I. M. (2008). ATL-1, an analogue of aspirin-triggered lipoxin A4, is a potent inhibitor of several steps in angiogenesis induced by vascular endothelial growth factor. British Journal of Pharmacology, 153(5), 956–965.PubMed Cezar-de-Mello, P. F. T., Vieira, A. M., Nascimento-Silva, V., Villela, C. G., Barja-Fidalgo, C., & Fierro, I. M. (2008). ATL-1, an analogue of aspirin-triggered lipoxin A4, is a potent inhibitor of several steps in angiogenesis induced by vascular endothelial growth factor. British Journal of Pharmacology, 153(5), 956–965.PubMed
71.
go back to reference Kantarci, A., Blackwood, A., Hasturk, H., Serhan, C.N., Van, T.E. Dyke. (2008). Resolvin-E1 and lipoxin-A4 control pro-inflammatory PMN functions in diabetes. In IDAR 86 th Periodontal Research-Pathogenesis. Poster # 2736. Kantarci, A., Blackwood, A., Hasturk, H., Serhan, C.N., Van, T.E. Dyke. (2008). Resolvin-E1 and lipoxin-A4 control pro-inflammatory PMN functions in diabetes. In IDAR 86 th Periodontal Research-Pathogenesis. Poster # 2736.
72.
go back to reference Gewirtz, A. T., Collier-Hyams, L. S., Young, A. N., Kucharzik, T., Guilford, W. J., Parkinson, J. F., et al. (2002). Lipoxin A4 analogs attenuate induction of intestinal epithelial proinflammatory gene expression and reduce the severity of dextran sodium sulfate-induced colitis. Journal of Immunology, 168(10), 5260–5267. Gewirtz, A. T., Collier-Hyams, L. S., Young, A. N., Kucharzik, T., Guilford, W. J., Parkinson, J. F., et al. (2002). Lipoxin A4 analogs attenuate induction of intestinal epithelial proinflammatory gene expression and reduce the severity of dextran sodium sulfate-induced colitis. Journal of Immunology, 168(10), 5260–5267.
73.
go back to reference Chiang, N., Serhan, C. N., Dahle’n, S. E., Drazen, J. M., Hay, D. W., Rovati, G. E., et al. (2006). The lipoxin receptor ALX: potent ligand-specific and stereoselective actions in vivo. Pharmacology Reviews, 58, 463–487. Chiang, N., Serhan, C. N., Dahle’n, S. E., Drazen, J. M., Hay, D. W., Rovati, G. E., et al. (2006). The lipoxin receptor ALX: potent ligand-specific and stereoselective actions in vivo. Pharmacology Reviews, 58, 463–487.
74.
go back to reference Ye, R. D., Boulay, F., Wang, J. M., Dahlgren, C., Gerard, C., Parmentier, M., et al. (2009). International Union of Basic and Clinical Pharmacology. LXXIII. Nomenclature for the formyl peptide receptor (FPR) family. Pharmacology Reviews, 61, 119–161. Ye, R. D., Boulay, F., Wang, J. M., Dahlgren, C., Gerard, C., Parmentier, M., et al. (2009). International Union of Basic and Clinical Pharmacology. LXXIII. Nomenclature for the formyl peptide receptor (FPR) family. Pharmacology Reviews, 61, 119–161.
75.
go back to reference Hachicha, M., Pouliot, M., Petasis, N. A., & Serhan, C. N. (1999). Lipoxin (LX) A4 and aspirin-triggered 15-epi-LXA4 inhibit tumor necrosis factor 1_-inhibited neutrophil responses and trafficking: regulators of a cytokine-chemokine axis. The Journal of Experimental Medicine, 189, 1923–1930.PubMed Hachicha, M., Pouliot, M., Petasis, N. A., & Serhan, C. N. (1999). Lipoxin (LX) A4 and aspirin-triggered 15-epi-LXA4 inhibit tumor necrosis factor 1_-inhibited neutrophil responses and trafficking: regulators of a cytokine-chemokine axis. The Journal of Experimental Medicine, 189, 1923–1930.PubMed
76.
go back to reference Wu, S. H., Liao, P. Y., Don, L., & Chen, Z. Q. (2008). Signal pathway involved in inhibition by lipoxin A4 of production of interleukins induced in endothelial cells by lipopolysaccharide. Inflammation Research, 57, 430–437.PubMed Wu, S. H., Liao, P. Y., Don, L., & Chen, Z. Q. (2008). Signal pathway involved in inhibition by lipoxin A4 of production of interleukins induced in endothelial cells by lipopolysaccharide. Inflammation Research, 57, 430–437.PubMed
77.
go back to reference Levy, B. D., Bonnans, C., Silverman, E. S., Palmer, L. J., Marigowda, G., & Israel, E. (2005). Severe Asthma Research Program, National Heart, Lung, and Blood Institute Diminished lipoxin biosynthesis in severe asthma. American Journal of Respiratory and Critical Care Medicine, 172, 824–830.PubMed Levy, B. D., Bonnans, C., Silverman, E. S., Palmer, L. J., Marigowda, G., & Israel, E. (2005). Severe Asthma Research Program, National Heart, Lung, and Blood Institute Diminished lipoxin biosynthesis in severe asthma. American Journal of Respiratory and Critical Care Medicine, 172, 824–830.PubMed
78.
go back to reference Levy, B. D., Lukacs, N. W., Berlin, A. A., Schmidt, B., Guilford, W. J., Serhan, C. N., et al. (2007). Lipoxin A4 stable analogs reduce allergic airway responses via mechanisms distinct from CysLT1 receptor antagonism. Journal of the Federation of American Societies for Experimental Biology, 21, 3877–3884. Levy, B. D., Lukacs, N. W., Berlin, A. A., Schmidt, B., Guilford, W. J., Serhan, C. N., et al. (2007). Lipoxin A4 stable analogs reduce allergic airway responses via mechanisms distinct from CysLT1 receptor antagonism. Journal of the Federation of American Societies for Experimental Biology, 21, 3877–3884.
79.
go back to reference Fiorucci, S., Wallace, J. L., Mencarelli, A., Distrutti, E., Rizzo, G., Farneti, S., et al. (2004). A-oxidation-resistant lipoxin A4 analog treats hapten-induced colitis by attenuating inflammation and immune dysfunction. Proceedings of National Academy of Sciences, 101, 15736–15741. Fiorucci, S., Wallace, J. L., Mencarelli, A., Distrutti, E., Rizzo, G., Farneti, S., et al. (2004). A-oxidation-resistant lipoxin A4 analog treats hapten-induced colitis by attenuating inflammation and immune dysfunction. Proceedings of National Academy of Sciences, 101, 15736–15741.
80.
go back to reference Gronert, K., Gewirt, Z. A., Madara, J. L., & Serhan, C. N. (1998). Identification of a human enterocyte lipoxin A4 receptor that is regulated by interleukin (IL)-13 and interferon and inhibits tumor necrosis factor -induced IL-8 release. The Journal of Experimental Medicine, 187, 1285–1294.PubMed Gronert, K., Gewirt, Z. A., Madara, J. L., & Serhan, C. N. (1998). Identification of a human enterocyte lipoxin A4 receptor that is regulated by interleukin (IL)-13 and interferon and inhibits tumor necrosis factor -induced IL-8 release. The Journal of Experimental Medicine, 187, 1285–1294.PubMed
81.
go back to reference Kure, I., Nishiumi, S., Nishitani, Y., Tanoue, T., Ishida, T., Mizuno, M., et al. (2010). Lipoxin A4 reduces lipopolysaccharide-induced inflammation in macrophages and intestinal epithelial cells through inhibition of nuclear factor-_B activation. The Journal of Pharmacology and Experimental Therapeutics, 332, 541–548.PubMed Kure, I., Nishiumi, S., Nishitani, Y., Tanoue, T., Ishida, T., Mizuno, M., et al. (2010). Lipoxin A4 reduces lipopolysaccharide-induced inflammation in macrophages and intestinal epithelial cells through inhibition of nuclear factor-_B activation. The Journal of Pharmacology and Experimental Therapeutics, 332, 541–548.PubMed
82.
go back to reference Ohkawara, T., Mitsuyama, K., Takeda, H., Asaka, M., Fujiyama, Y., & Nishihira, J. (2008). Lack of macrophage migration inhibitory factor suppresses innate immune response in murine dextran sulfate sodium-induced colitis. Scandinavian Journal of Gastroenterology, 43, 1497–1504.PubMed Ohkawara, T., Mitsuyama, K., Takeda, H., Asaka, M., Fujiyama, Y., & Nishihira, J. (2008). Lack of macrophage migration inhibitory factor suppresses innate immune response in murine dextran sulfate sodium-induced colitis. Scandinavian Journal of Gastroenterology, 43, 1497–1504.PubMed
83.
go back to reference Andrew, T., McCormick, B. G., Neish, S. A., Petasis, A. N., Gronert, K., Serhan, C. N., et al. (1998). Pathogen-induced chemokine secretion from model intestinal epithelium is inhibited by lipoxin A4 analogs. Journal of Clinical Investigations, 101, 1860–1869. Andrew, T., McCormick, B. G., Neish, S. A., Petasis, A. N., Gronert, K., Serhan, C. N., et al. (1998). Pathogen-induced chemokine secretion from model intestinal epithelium is inhibited by lipoxin A4 analogs. Journal of Clinical Investigations, 101, 1860–1869.
84.
go back to reference Serhan, C. N., et al. (2002). Resolvins: a family of bioactive products of omega-3 fatty acid transformation circuits initiated by aspirin treatment that counter proinflammation signals. The Journal of Experimental Medicine, 196, 1025–1037.PubMed Serhan, C. N., et al. (2002). Resolvins: a family of bioactive products of omega-3 fatty acid transformation circuits initiated by aspirin treatment that counter proinflammation signals. The Journal of Experimental Medicine, 196, 1025–1037.PubMed
85.
go back to reference Arita, M., et al. (2005). Resolvin E1, an endogenous lipid mediator derived from omega-3 eicosapentaenoic acid, protects against 2,4,6-trinitrobenzene sulfonic acid-induced colitis. Proceedings of the National Academy of Sciences, 102, 7671–7676. Arita, M., et al. (2005). Resolvin E1, an endogenous lipid mediator derived from omega-3 eicosapentaenoic acid, protects against 2,4,6-trinitrobenzene sulfonic acid-induced colitis. Proceedings of the National Academy of Sciences, 102, 7671–7676.
86.
go back to reference Hudert, C. A., et al. (2006). Transgenic mice rich in endogenous omega-3 fatty acids are protected from colitis. Proceedings of the National Academy of Sciences, 103, 11276–11281. Hudert, C. A., et al. (2006). Transgenic mice rich in endogenous omega-3 fatty acids are protected from colitis. Proceedings of the National Academy of Sciences, 103, 11276–11281.
87.
go back to reference Campbell, E. L., Louis, N. A., Tomassetti, S. E., Canny, G. O., Arita, M., Serhan, C. N., et al. (2007). Resolvin E1 promotes mucosal surface clearance of neutrophils: a new paradigm for inflammatory resolution. Federation of American Society for Experimental Biology Journal, 21, 3162–3170. Campbell, E. L., Louis, N. A., Tomassetti, S. E., Canny, G. O., Arita, M., Serhan, C. N., et al. (2007). Resolvin E1 promotes mucosal surface clearance of neutrophils: a new paradigm for inflammatory resolution. Federation of American Society for Experimental Biology Journal, 21, 3162–3170.
88.
go back to reference Ishida, T., Yoshida, M., Arita, M., Nishitani, Y., Nishiumi, S., Masuda, A., et al. (2010). Resolvin E1, an endogenous lipid mediator derived from eicosapentaenoic acid, prevents dextran sulfate sodium-induced colitis. Inflammatory Bowel Disease, 16, 87–95. Ishida, T., Yoshida, M., Arita, M., Nishitani, Y., Nishiumi, S., Masuda, A., et al. (2010). Resolvin E1, an endogenous lipid mediator derived from eicosapentaenoic acid, prevents dextran sulfate sodium-induced colitis. Inflammatory Bowel Disease, 16, 87–95.
89.
go back to reference Campbell, L. E., MacManus, F. C., Kominsky, J. D., Keely, S., Glover, E. L., Bowers, E. B., et al. (2010). Resolvin E1-induced intestinal alkaline phosphatase promotes resolution of inflammation through LPS detoxification. Proceedings of the National Academy of Sciences of the United States of America, 107, 14298–14303. doi:10.1073/pnas.0914730107.PubMed Campbell, L. E., MacManus, F. C., Kominsky, J. D., Keely, S., Glover, E. L., Bowers, E. B., et al. (2010). Resolvin E1-induced intestinal alkaline phosphatase promotes resolution of inflammation through LPS detoxification. Proceedings of the National Academy of Sciences of the United States of America, 107, 14298–14303. doi:10.​1073/​pnas.​0914730107.PubMed
90.
go back to reference Aoki, H., Hisada, T., Ishizuka, T., Utsugi, M., Kawata, T., Shimizu, Y., et al. (2008). Resolvin E1 dampens airway inflammation and hyperresponsiveness in a murine model of asthma. Biochemical and Biophysical Research Communications, 367, 509–515.PubMed Aoki, H., Hisada, T., Ishizuka, T., Utsugi, M., Kawata, T., Shimizu, Y., et al. (2008). Resolvin E1 dampens airway inflammation and hyperresponsiveness in a murine model of asthma. Biochemical and Biophysical Research Communications, 367, 509–515.PubMed
91.
go back to reference Nieto, N., Torres, M. I., Ríos, A., & Gil, A. (2002). Dietary polyunsaturated fatty acids improve histological and biochemical alterations in rats with experimental ulcerative colitis. Journal of Nutrition, 132, 11–19.PubMed Nieto, N., Torres, M. I., Ríos, A., & Gil, A. (2002). Dietary polyunsaturated fatty acids improve histological and biochemical alterations in rats with experimental ulcerative colitis. Journal of Nutrition, 132, 11–19.PubMed
92.
go back to reference Ishida, T., Yoshida, M., Arita, M., Nishitani, Y., Nishiumi, S., Masuda, A., et al. (2009). Resolvin E1, an endogenous lipid mediator derived from eicosapentaenoic acid, prevents dextran sulfate sodium-induced colitis. Inflammation and Bowel Diseases, 16(1), 87–95. doi:10.1002/ibd.21029. Ishida, T., Yoshida, M., Arita, M., Nishitani, Y., Nishiumi, S., Masuda, A., et al. (2009). Resolvin E1, an endogenous lipid mediator derived from eicosapentaenoic acid, prevents dextran sulfate sodium-induced colitis. Inflammation and Bowel Diseases, 16(1), 87–95. doi:10.​1002/​ibd.​21029.
93.
go back to reference Cheng, Y., Austin, S. C., Rocca, B., Koller, B. H., Coffman, T. M., Grosser, T., et al. (2002). Role of prostacyclin in the cardiovascular response to thromboxane A2. Science, 296, 539–541.PubMed Cheng, Y., Austin, S. C., Rocca, B., Koller, B. H., Coffman, T. M., Grosser, T., et al. (2002). Role of prostacyclin in the cardiovascular response to thromboxane A2. Science, 296, 539–541.PubMed
94.
go back to reference Lund, T., Mangsbo, S. M., Scholz, H., Gjorstrup, P., Tötterman, T. H., Korsgren, O., et al. (2010). Resolvin E1 reduces proinflammatory markers in human pancreatic islets in vitro. Experiments in Clinical Endocrinology and Diabetes., 118(4), 237–244. Lund, T., Mangsbo, S. M., Scholz, H., Gjorstrup, P., Tötterman, T. H., Korsgren, O., et al. (2010). Resolvin E1 reduces proinflammatory markers in human pancreatic islets in vitro. Experiments in Clinical Endocrinology and Diabetes., 118(4), 237–244.
95.
go back to reference Crawford, M., Galli, C., Visioli, F., Renaud, S., Simopoulos, A. P., & Spector, A. A. (2000). Role of plant-derived omega-3 fatty acids in human nutrition. Annals of Nutrition and Metabolism, 44, 263–265.PubMed Crawford, M., Galli, C., Visioli, F., Renaud, S., Simopoulos, A. P., & Spector, A. A. (2000). Role of plant-derived omega-3 fatty acids in human nutrition. Annals of Nutrition and Metabolism, 44, 263–265.PubMed
96.
go back to reference Rose, D. P., & Connolly, J. M. (1999). Omega-3 fatty acids as cancer chemopreventive agents. Pharmacology and Therapeutics, 83, 217–244.PubMed Rose, D. P., & Connolly, J. M. (1999). Omega-3 fatty acids as cancer chemopreventive agents. Pharmacology and Therapeutics, 83, 217–244.PubMed
97.
go back to reference Ringbom, T., Huss, U., Stenholm, A., et al. (2001). Cox-2 inhibitory effects of naturally occurring and modified fatty acids. Journal of Natural Products, 64, 745–749.PubMed Ringbom, T., Huss, U., Stenholm, A., et al. (2001). Cox-2 inhibitory effects of naturally occurring and modified fatty acids. Journal of Natural Products, 64, 745–749.PubMed
98.
go back to reference Singh, J., Hamid, R., & Reddy, B. S. (1997). Dietary fat and colon cancer: modulation of cyclooxygenase-2 by types and amount of dietary fat during the postinitiation stage of colon carcinogenesis. Cancer Research, 57, 3465–3470.PubMed Singh, J., Hamid, R., & Reddy, B. S. (1997). Dietary fat and colon cancer: modulation of cyclooxygenase-2 by types and amount of dietary fat during the postinitiation stage of colon carcinogenesis. Cancer Research, 57, 3465–3470.PubMed
99.
go back to reference Culp, B. R., Titus, B. G., & Lands, W. E. (1979). Inhibition of prostaglandin biosynthesis by eicosapentaenoic acid. Prostaglandins and Medicine, 3, 269–278.PubMed Culp, B. R., Titus, B. G., & Lands, W. E. (1979). Inhibition of prostaglandin biosynthesis by eicosapentaenoic acid. Prostaglandins and Medicine, 3, 269–278.PubMed
100.
go back to reference Marshall, L. A., & Johnston, P. V. (1982). Modulation of tissue prostaglandin synthesizing capacity by increased ratios of dietary alpha-linolenic acid to linoleic acid. Lipids, 17, 905–913.PubMed Marshall, L. A., & Johnston, P. V. (1982). Modulation of tissue prostaglandin synthesizing capacity by increased ratios of dietary alpha-linolenic acid to linoleic acid. Lipids, 17, 905–913.PubMed
101.
go back to reference Corey, E. J., Shih, C., & Cashman, J. R. (1983). Docosahexaenoic acid is a strong inhibitor of prostaglandin but not leukotriene biosynthesis. Proceedings of the National Academy of Sciences, 80, 3581–3584. Corey, E. J., Shih, C., & Cashman, J. R. (1983). Docosahexaenoic acid is a strong inhibitor of prostaglandin but not leukotriene biosynthesis. Proceedings of the National Academy of Sciences, 80, 3581–3584.
102.
go back to reference Grimm, H., Mayer, K., Mayser, P., & Eigenbrodt, E. (2002). Regulatory poten Yoshimura al of n_3 fatty acids in immunological and inflammatory processes. British Journal of Nutrition, 87(suppl), S59–S67.PubMed Grimm, H., Mayer, K., Mayser, P., & Eigenbrodt, E. (2002). Regulatory poten Yoshimura al of n_3 fatty acids in immunological and inflammatory processes. British Journal of Nutrition, 87(suppl), S59–S67.PubMed
103.
go back to reference Von Schacky, C., Kiefl, R., Marcus, A. J., Broekman, M. J., & Kaminski, W. E. (1993). Dietary n_3 fatty acids accelerate catabolism of leukotriene B4 in human granulocytes. Biochimica et Biophysica Acta, 1166, 20–24. Von Schacky, C., Kiefl, R., Marcus, A. J., Broekman, M. J., & Kaminski, W. E. (1993). Dietary n_3 fatty acids accelerate catabolism of leukotriene B4 in human granulocytes. Biochimica et Biophysica Acta, 1166, 20–24.
104.
go back to reference Tsunomori, M., Fujimoto, Y., Muta, E., Nishida, H., Sakuma, S., & Fujita, T. (1996). 15-Hydroperoxyeicosapentaenoic acid inhibits arachidonic acid metabolism in rabbit platelets more potently than eicosapentaenoic acid. Biochimica et Biophysica Acta, 1300, 171–176.PubMed Tsunomori, M., Fujimoto, Y., Muta, E., Nishida, H., Sakuma, S., & Fujita, T. (1996). 15-Hydroperoxyeicosapentaenoic acid inhibits arachidonic acid metabolism in rabbit platelets more potently than eicosapentaenoic acid. Biochimica et Biophysica Acta, 1300, 171–176.PubMed
105.
go back to reference Collett, E. D., Davidson, L. A., Fan, Y. Y., Lupton, J. R., & Chapkin, R. S. (2001). n_6 And n_3 polyunsaturated fatty acids differentially modulate oncogenic Ras activation in colonocytes. American Journal of Physiology, 280, C1066–C1075.PubMed Collett, E. D., Davidson, L. A., Fan, Y. Y., Lupton, J. R., & Chapkin, R. S. (2001). n_6 And n_3 polyunsaturated fatty acids differentially modulate oncogenic Ras activation in colonocytes. American Journal of Physiology, 280, C1066–C1075.PubMed
106.
go back to reference Chang, W. L., Chapkin, R. S., & Lupton, J. R. (1998). Fish oil blocks azoxymethane induced rat colon tumorigenesis by increasing cell differentiation and apoptosis rather than decreasing cell proliferation. Journal of Nutrition, 128, 491–497.PubMed Chang, W. L., Chapkin, R. S., & Lupton, J. R. (1998). Fish oil blocks azoxymethane induced rat colon tumorigenesis by increasing cell differentiation and apoptosis rather than decreasing cell proliferation. Journal of Nutrition, 128, 491–497.PubMed
107.
go back to reference Murray, N. R., Weems, C., Chen, L., et al. (2002). Protein kinase C betaII and TGFbetaRII in omega-3 fatty acid-mediated inhibition of colon carcinogenesis. The Journal of Cell Biology, 157, 915–920.PubMed Murray, N. R., Weems, C., Chen, L., et al. (2002). Protein kinase C betaII and TGFbetaRII in omega-3 fatty acid-mediated inhibition of colon carcinogenesis. The Journal of Cell Biology, 157, 915–920.PubMed
108.
go back to reference Murray, N. R., Davidson, L. A., Chapkin, R. S., Clay Gustafson, W., Schattenberg, D. G., & Fields, A. P. (1999). Overexpression of protein kinase C betaII induces colonic hyperproliferation and increased sensitivity to colon carcinogenesis. The Journal of Cell Biology, 145, 699–711.PubMed Murray, N. R., Davidson, L. A., Chapkin, R. S., Clay Gustafson, W., Schattenberg, D. G., & Fields, A. P. (1999). Overexpression of protein kinase C betaII induces colonic hyperproliferation and increased sensitivity to colon carcinogenesis. The Journal of Cell Biology, 145, 699–711.PubMed
109.
go back to reference Gokmen-Polar, Y., Murray, N. R., Velasco, M. A., Gatalica, Z., & Fields, A. P. (2001). Elevated protein kinase C betaII is an early promotive event in colon carcinogenesis. Cancer Research, 61, 1375–1381.PubMed Gokmen-Polar, Y., Murray, N. R., Velasco, M. A., Gatalica, Z., & Fields, A. P. (2001). Elevated protein kinase C betaII is an early promotive event in colon carcinogenesis. Cancer Research, 61, 1375–1381.PubMed
110.
go back to reference Roeder, C., Kalthoff, H., Henne-Bruns, D., & Kremer, B. (1995). Expression of the cytokines interleukin-113 and GM-CSF in pancreatic tumor cells is stimulated by tumor necrosis factor-et via different mechanisms. In G. Hierholzer, J. Seifert, & W. Hartel (Eds.), Chirurgisches Forum f. Experim. u. klinische Forschung (pp. 505–508). Berlin: Springer. Roeder, C., Kalthoff, H., Henne-Bruns, D., & Kremer, B. (1995). Expression of the cytokines interleukin-113 and GM-CSF in pancreatic tumor cells is stimulated by tumor necrosis factor-et via different mechanisms. In G. Hierholzer, J. Seifert, & W. Hartel (Eds.), Chirurgisches Forum f. Experim. u. klinische Forschung (pp. 505–508). Berlin: Springer.
111.
go back to reference Glick, A. B., Sporn, M. B., & Yuspa, S. H. (1991). Altered regulation of TGF-beta 1 and TGF-alpha in primary keratinocytes and papillomas expressing v-Ha-ras. Molecular Carcinogenesis, 4, 210–219.PubMed Glick, A. B., Sporn, M. B., & Yuspa, S. H. (1991). Altered regulation of TGF-beta 1 and TGF-alpha in primary keratinocytes and papillomas expressing v-Ha-ras. Molecular Carcinogenesis, 4, 210–219.PubMed
112.
go back to reference Kalthoff, H., Roeder, C., & Schmiegel, W. (1993). Cytokine-mediated regulation of growth factor receptors (EGF-R and erb-B2) in pancreatic tumors. In C. Wagener & M. Neumann (Eds.), Molecular diagnostics of cancer (pp. 175–186). Berlin: Springer. Kalthoff, H., Roeder, C., & Schmiegel, W. (1993). Cytokine-mediated regulation of growth factor receptors (EGF-R and erb-B2) in pancreatic tumors. In C. Wagener & M. Neumann (Eds.), Molecular diagnostics of cancer (pp. 175–186). Berlin: Springer.
113.
go back to reference Kleeff, J., Kusama, T., Rossi, D. L., Ishiwata, T., Maruyama, H., Friess, H., et al. (1999). Detection and localization of Mip-3alpha/LARC/Exodus, a macrophage proinflammatory chemokine, and its CCR6 receptor in human pancreatic cancer. International Journal of Cancer, 81, 650–665. Kleeff, J., Kusama, T., Rossi, D. L., Ishiwata, T., Maruyama, H., Friess, H., et al. (1999). Detection and localization of Mip-3alpha/LARC/Exodus, a macrophage proinflammatory chemokine, and its CCR6 receptor in human pancreatic cancer. International Journal of Cancer, 81, 650–665.
114.
go back to reference Farrow, B., Sugiyama, Y., Chen, A., Uffort, E., Nealon, W., & Mark Evers, B. (2004). Inflammatory mechanisms contributing to pancreatic cancer development. Annals of Surgery, 239, 763–769.PubMed Farrow, B., Sugiyama, Y., Chen, A., Uffort, E., Nealon, W., & Mark Evers, B. (2004). Inflammatory mechanisms contributing to pancreatic cancer development. Annals of Surgery, 239, 763–769.PubMed
115.
go back to reference Kuwada, Y., Sasaki, T., Morinaka, K., Kitadai, Y., Mukaida, N., & Chayama, K. (2003). Potential involvement of IL-8 and its receptors in the invasiveness of pancreatic cancer cells. International Journal of Oncology, 22, 765–771.PubMed Kuwada, Y., Sasaki, T., Morinaka, K., Kitadai, Y., Mukaida, N., & Chayama, K. (2003). Potential involvement of IL-8 and its receptors in the invasiveness of pancreatic cancer cells. International Journal of Oncology, 22, 765–771.PubMed
116.
go back to reference Xiong, Q., Shi, Q., Le, X., Wang, B., & Xie, K. (2001). Regulation of interleukin-8 expression by nitric oxide in human pancreatic adenocarcinoma. Journal of Interferon and Cytokine Research, 21, 529–537.PubMed Xiong, Q., Shi, Q., Le, X., Wang, B., & Xie, K. (2001). Regulation of interleukin-8 expression by nitric oxide in human pancreatic adenocarcinoma. Journal of Interferon and Cytokine Research, 21, 529–537.PubMed
117.
go back to reference Muerkoster, S., Wegehenkel, K., Arlt, A., Witt, M., Sipos, B., Kruse, M. L., et al. (2004). Tumor stroma interactions induce chemoresistance in pancreatic ductal carcinoma cells involving increased secretion and paracrine effects of nitric oxide and interleukin-1beta. Cancer Research, 64, 1331–1337.PubMed Muerkoster, S., Wegehenkel, K., Arlt, A., Witt, M., Sipos, B., Kruse, M. L., et al. (2004). Tumor stroma interactions induce chemoresistance in pancreatic ductal carcinoma cells involving increased secretion and paracrine effects of nitric oxide and interleukin-1beta. Cancer Research, 64, 1331–1337.PubMed
118.
go back to reference Marchesi, F., Monti, P., Leone, B. E., Zerbi, A., Vecchi, A., Piemonti, L., et al. (2004). Increased survival, proliferation, and migration in metastatic human pancreatic tumor cells expressing functional CXCR4. Cancer Research, 64, 8420–8427.PubMed Marchesi, F., Monti, P., Leone, B. E., Zerbi, A., Vecchi, A., Piemonti, L., et al. (2004). Increased survival, proliferation, and migration in metastatic human pancreatic tumor cells expressing functional CXCR4. Cancer Research, 64, 8420–8427.PubMed
119.
go back to reference Greten, F. R., Eckmann, L., Greten, T. F., Park, J. M., Li, Z. W., Egan, L. J., et al. (2004). IKKbeta links inflammation and tumorigenesis in a mouse model of colitis-associated cancer. Cell, 118, 285–296.PubMed Greten, F. R., Eckmann, L., Greten, T. F., Park, J. M., Li, Z. W., Egan, L. J., et al. (2004). IKKbeta links inflammation and tumorigenesis in a mouse model of colitis-associated cancer. Cell, 118, 285–296.PubMed
120.
go back to reference Becker, C., Fantini, M. C., Wirtz, S., et al. (2005). IL-6 signaling promotes tumor growth in colorectal cancer. Cell Cycle, 4, 217–220.PubMed Becker, C., Fantini, M. C., Wirtz, S., et al. (2005). IL-6 signaling promotes tumor growth in colorectal cancer. Cell Cycle, 4, 217–220.PubMed
121.
go back to reference Grivennikov, S., Karin, E., Terzic, J., Mucida, D., Yu, G. Y., Vallabhapurapu, S., et al. (2009). IL-6 and Stat3 are required for survival of intestinal epithelial cells and development of colitis-associated cancer. Cancer Cell, 15, 103–113.PubMed Grivennikov, S., Karin, E., Terzic, J., Mucida, D., Yu, G. Y., Vallabhapurapu, S., et al. (2009). IL-6 and Stat3 are required for survival of intestinal epithelial cells and development of colitis-associated cancer. Cancer Cell, 15, 103–113.PubMed
122.
go back to reference Matsumoto, S., Hara, T., Mitsuyama, K., et al. (2010). Essential roles of IL-6 trans-signaling in colonic epithelial cells, induced by the IL-6/soluble-IL-6 receptor derived from lamina propria macrophages, on the development of colitis-associated premalignant cancer in a murine model. Journal of Immunology, 184, 1543–1551. Matsumoto, S., Hara, T., Mitsuyama, K., et al. (2010). Essential roles of IL-6 trans-signaling in colonic epithelial cells, induced by the IL-6/soluble-IL-6 receptor derived from lamina propria macrophages, on the development of colitis-associated premalignant cancer in a murine model. Journal of Immunology, 184, 1543–1551.
123.
go back to reference Becker, C., Fantini, M. C., Schramm, C., et al. (2004). TGF-beta suppresses tumor progression in colon cancer by inhibition of IL-6 trans-signaling. Immunity, 21, 491–501.PubMed Becker, C., Fantini, M. C., Schramm, C., et al. (2004). TGF-beta suppresses tumor progression in colon cancer by inhibition of IL-6 trans-signaling. Immunity, 21, 491–501.PubMed
124.
go back to reference Ring, W. L., Riddick, C. A., Baker, J. R., Munafo, D. A., & Bigby, T. D. (1996). Lymphocytes stimulate expression of 5-lipoxygenase and its activating protein in monocytes in vitro via granulocyte–macrophage colony stimulating factor and interleukin-3. Journal of Clinical Investigations, 97, 1293–1301. Ring, W. L., Riddick, C. A., Baker, J. R., Munafo, D. A., & Bigby, T. D. (1996). Lymphocytes stimulate expression of 5-lipoxygenase and its activating protein in monocytes in vitro via granulocyte–macrophage colony stimulating factor and interleukin-3. Journal of Clinical Investigations, 97, 1293–1301.
125.
go back to reference Feltenmark, S., Runarsson, C., Larsson, P., Jakobsson, P-i, Bjorkholm, M., & Claesson, H.-E. (1995). Diverse expression of cytosolic phospholipase A2, 5-lipoxygenase and prostaglandin H synthase 2 in acute pre-B-lymphocytic leukaemia ce1is. British Journal of Haematology, 90, 585–594.PubMed Feltenmark, S., Runarsson, C., Larsson, P., Jakobsson, P-i, Bjorkholm, M., & Claesson, H.-E. (1995). Diverse expression of cytosolic phospholipase A2, 5-lipoxygenase and prostaglandin H synthase 2 in acute pre-B-lymphocytic leukaemia ce1is. British Journal of Haematology, 90, 585–594.PubMed
126.
go back to reference Nassar, C. M., Morrow, J. D., Roberts, L. J., II, Lakkis, F. C., & Badr, K. F. (1994). Induction of l5-lipoxygenase by interleukin-13 in human blood monocytes. Journal of Biological Chemistry, 269(2763), 1–27634. Nassar, C. M., Morrow, J. D., Roberts, L. J., II, Lakkis, F. C., & Badr, K. F. (1994). Induction of l5-lipoxygenase by interleukin-13 in human blood monocytes. Journal of Biological Chemistry, 269(2763), 1–27634.
127.
go back to reference Stenke, L., Reizenstein, P., & Lindgren, J. A. (1994). Leukotrienes and lipoxins—new potential performers in the regulation of human myelopoiesis. Leukemia Research, 18, 727–732.PubMed Stenke, L., Reizenstein, P., & Lindgren, J. A. (1994). Leukotrienes and lipoxins—new potential performers in the regulation of human myelopoiesis. Leukemia Research, 18, 727–732.PubMed
128.
go back to reference Erreni, M., Bianchi, P., Laghi, L., Mirolo, M., Fabbri, M., Locati, M., et al. (2009). Expression of chemokines and chemokine receptors in human colon cancer. Methods in Enzymology, 460, 105–121.PubMed Erreni, M., Bianchi, P., Laghi, L., Mirolo, M., Fabbri, M., Locati, M., et al. (2009). Expression of chemokines and chemokine receptors in human colon cancer. Methods in Enzymology, 460, 105–121.PubMed
129.
go back to reference Kollias, G. (2004). Modeling the function of tumor necrosis factor in immune pathophysiology. Autoimmunity Reviews, 3(Suppl 1), S24–S25.PubMed Kollias, G. (2004). Modeling the function of tumor necrosis factor in immune pathophysiology. Autoimmunity Reviews, 3(Suppl 1), S24–S25.PubMed
130.
go back to reference Grivennikov, S. I., Tumanov, A. V., Liepinsh, D. J., et al. (2005). Distinct and nonredundant in vivo functions of TNF produced by t cells and macrophages/neutrophils: protective and deleterious effects. Immunity, 22, 93–104.PubMed Grivennikov, S. I., Tumanov, A. V., Liepinsh, D. J., et al. (2005). Distinct and nonredundant in vivo functions of TNF produced by t cells and macrophages/neutrophils: protective and deleterious effects. Immunity, 22, 93–104.PubMed
131.
go back to reference Popivanova, B. K., Kitamura, K., Wu, Y., Kondo, T., Kagaya, T., Kaneko, S., et al. (2008). Blocking sTNF-alpha in mice reduces colorectal carcinogenesis associated with chronic colitis. Journal of Clinical Investigation, 118, 560–570.PubMed Popivanova, B. K., Kitamura, K., Wu, Y., Kondo, T., Kagaya, T., Kaneko, S., et al. (2008). Blocking sTNF-alpha in mice reduces colorectal carcinogenesis associated with chronic colitis. Journal of Clinical Investigation, 118, 560–570.PubMed
132.
go back to reference Prescott, S. M., Zimmerman, G. A., Stafforini, D. M., et al. (2000). Platelet-activating factor and related lipid mediators. Annual Reviews in Biochemistry, 69, 419–445. Prescott, S. M., Zimmerman, G. A., Stafforini, D. M., et al. (2000). Platelet-activating factor and related lipid mediators. Annual Reviews in Biochemistry, 69, 419–445.
133.
go back to reference Ko, H. M., Jung, H. H., Seo, K. H., et al. (2006). Platelet-activating factor-induced NF-kappaB activation enhances VEGF expression through a decrease in p53 activity. Federation of the Societies of Biochemistry and Molecular Biology- Letters, 580, 3006–3012. Ko, H. M., Jung, H. H., Seo, K. H., et al. (2006). Platelet-activating factor-induced NF-kappaB activation enhances VEGF expression through a decrease in p53 activity. Federation of the Societies of Biochemistry and Molecular Biology- Letters, 580, 3006–3012.
134.
go back to reference Biancone, L., Cantaluppi, V., Del Sorbo, L., et al. (2003). Platelet-activating factor inactivation by local expression of platelet-activating factor acetyl-hydrolase modifies tumor vascularization and growth. Clinical Cancer Research, 9, 4214–4220.PubMed Biancone, L., Cantaluppi, V., Del Sorbo, L., et al. (2003). Platelet-activating factor inactivation by local expression of platelet-activating factor acetyl-hydrolase modifies tumor vascularization and growth. Clinical Cancer Research, 9, 4214–4220.PubMed
135.
go back to reference Griffiths, R. J. (1999). Prostaglandins and inflammation. In J. I. Gallin & R. Snyderman (Eds.), Inflammation: basic principles and clinical correlates (pp. 249–265). Philadelphia: Lippincott & Wilkins. Griffiths, R. J. (1999). Prostaglandins and inflammation. In J. I. Gallin & R. Snyderman (Eds.), Inflammation: basic principles and clinical correlates (pp. 249–265). Philadelphia: Lippincott & Wilkins.
136.
go back to reference Dumont, P., Berton, A., Nagy, N., et al. (2008). Expression of galectin-3 in the tumor immune response in colon cancer. Laboratory Investigations, 88, 896–906. Dumont, P., Berton, A., Nagy, N., et al. (2008). Expression of galectin-3 in the tumor immune response in colon cancer. Laboratory Investigations, 88, 896–906.
Metadata
Title
Role of lipoxins, resolvins, and other bioactive lipids in colon and pancreatic cancer
Authors
Naveena B. Janakiram
Altaf Mohammed
Chinthalapally V. Rao
Publication date
01-12-2011
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 3-4/2011
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-011-9311-2

Other articles of this Issue 3-4/2011

Cancer and Metastasis Reviews 3-4/2011 Go to the issue

EditorialNotes

Preface

Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine