Skip to main content
Top
Published in: BMC Cancer 1/2010

Open Access 01-12-2010 | Research article

Role of 14-3-3σ in poor prognosis and in radiation and drug resistance of human pancreatic cancers

Authors: Zhaomin Li, Zizheng Dong, David Myer, Michele Yip-Schneider, Jianguo Liu, Ping Cui, C Max Schmidt, Jian-Ting Zhang

Published in: BMC Cancer | Issue 1/2010

Login to get access

Abstract

Background

Pancreatic cancer is the fourth leading cause of death in the US. Unlike other solid tumors such as testicular cancer which are now curable, more than 90% of pancreatic cancer patients die due to lack of response to therapy. Recently, the level of 14-3-3σ mRNA was found to be increased in pancreatic cancers and this increased expression may contribute to the failure in treatment of pancreatic cancers. In the present study, we tested this hypothesis.

Methods

Western blot analysis was used to determine 14-3-3σ protein level in fresh frozen tissues and was correlated to clinical outcome. A stable cell line expressing 14-3-3σ was established and the effect of 14-3-3σ over-expression on cellular response to radiation and anticancer drugs were tested using SRB assay and clonogenic assays. Cell cycle distribution and apoptosis analyses were performed using propidium iodide staining and PARP cleavage assays.

Results

We found that 14-3-3σ protein level was increased significantly in about 71% (17 of 24) of human pancreatic cancer tissues and that the 14-3-3σ protein level in cancers correlated with lymph node metastasis and poor prognosis. Furthermore, we demonstrated that over-expression of 14-3-3σ in a pancreatic cancer cell line caused resistance to γ-irradiation as well as anticancer drugs by causing resistance to treatment-induced apoptosis and G2/M arrest.

Conclusion

The increased level of 14-3-3σ protein likely contributes to the poor clinical outcome of human pancreatic cancers by causing resistance to radiation and anticancer drugs. Thus, 14-3-3σ may serve as a prognosis marker predicting survival of pancreatic cancer patients and guide the clinical treatment of these patients.
Appendix
Available only for authorised users
Literature
1.
go back to reference Fu H, Subramanian RR, Masters SC: 14-3-3 proteins: structure, function, and regulation. Annu Rev Pharmacol Toxicol. 2000, 40: 617-647. 10.1146/annurev.pharmtox.40.1.617.CrossRefPubMed Fu H, Subramanian RR, Masters SC: 14-3-3 proteins: structure, function, and regulation. Annu Rev Pharmacol Toxicol. 2000, 40: 617-647. 10.1146/annurev.pharmtox.40.1.617.CrossRefPubMed
2.
go back to reference Berg D, Holzmann C, Riess O: 14-3-3 proteins in the nervous system. Nat Rev Neurosci. 2003, 4 (9): 752-762. 10.1038/nrn1197.CrossRefPubMed Berg D, Holzmann C, Riess O: 14-3-3 proteins in the nervous system. Nat Rev Neurosci. 2003, 4 (9): 752-762. 10.1038/nrn1197.CrossRefPubMed
3.
go back to reference Li Z, Liu J-Y, Zhang J-T: 14-3-3σ, the double-edged sword of human cancers. American Journal of Translational Research. 2009, 1 (4): 326-340.PubMedPubMedCentral Li Z, Liu J-Y, Zhang J-T: 14-3-3σ, the double-edged sword of human cancers. American Journal of Translational Research. 2009, 1 (4): 326-340.PubMedPubMedCentral
4.
go back to reference Muslin AJ, Xing H: 14-3-3 proteins: regulation of subcellular localization by molecular interference. Cell Signal. 2000, 12 (11-12): 703-709. 10.1016/S0898-6568(00)00131-5.CrossRefPubMed Muslin AJ, Xing H: 14-3-3 proteins: regulation of subcellular localization by molecular interference. Cell Signal. 2000, 12 (11-12): 703-709. 10.1016/S0898-6568(00)00131-5.CrossRefPubMed
5.
go back to reference van Hemert MJ, Steensma HY, van Heusden GP: 14-3-3 proteins: key regulators of cell division, signalling and apoptosis. Bioessays. 2001, 23 (10): 936-946. 10.1002/bies.1134.CrossRefPubMed van Hemert MJ, Steensma HY, van Heusden GP: 14-3-3 proteins: key regulators of cell division, signalling and apoptosis. Bioessays. 2001, 23 (10): 936-946. 10.1002/bies.1134.CrossRefPubMed
6.
go back to reference Prasad GL, Valverius EM, McDuffie E, Cooper HL: Complementary DNA cloning of a novel epithelial cell marker protein, HME1, that may be down-regulated in neoplastic mammary cells. Cell Growth Differ. 1992, 3 (8): 507-513.PubMed Prasad GL, Valverius EM, McDuffie E, Cooper HL: Complementary DNA cloning of a novel epithelial cell marker protein, HME1, that may be down-regulated in neoplastic mammary cells. Cell Growth Differ. 1992, 3 (8): 507-513.PubMed
7.
go back to reference Hermeking H, Lengauer C, Polyak K, He TC, Zhang L, Thiagalingam S, Kinzler KW, Vogelstein B: 14-3-3 sigma is a p53-regulated inhibitor of G2/M progression. Mol Cell. 1997, 1 (1): 3-11. 10.1016/S1097-2765(00)80002-7.CrossRefPubMed Hermeking H, Lengauer C, Polyak K, He TC, Zhang L, Thiagalingam S, Kinzler KW, Vogelstein B: 14-3-3 sigma is a p53-regulated inhibitor of G2/M progression. Mol Cell. 1997, 1 (1): 3-11. 10.1016/S1097-2765(00)80002-7.CrossRefPubMed
8.
go back to reference Laronga C, Yang HY, Neal C, Lee MH: Association of the cyclin-dependent kinases and 14-3-3 sigma negatively regulates cell cycle progression. J Biol Chem. 2000, 275 (30): 23106-23112. 10.1074/jbc.M905616199.CrossRefPubMed Laronga C, Yang HY, Neal C, Lee MH: Association of the cyclin-dependent kinases and 14-3-3 sigma negatively regulates cell cycle progression. J Biol Chem. 2000, 275 (30): 23106-23112. 10.1074/jbc.M905616199.CrossRefPubMed
9.
go back to reference Liu Y, Liu H, Han B, Zhang JT: Identification of 14-3-3sigma as a contributor to drug resistance in human breast cancer cells using functional proteomic analysis. Cancer Res. 2006, 66 (6): 3248-3255. 10.1158/0008-5472.CAN-05-3801.CrossRefPubMed Liu Y, Liu H, Han B, Zhang JT: Identification of 14-3-3sigma as a contributor to drug resistance in human breast cancer cells using functional proteomic analysis. Cancer Res. 2006, 66 (6): 3248-3255. 10.1158/0008-5472.CAN-05-3801.CrossRefPubMed
10.
go back to reference Han B, Xie H, Chen Q, Zhang JT: Sensitizing hormone-refractory prostate cancer cells to drug treatment by targeting 14-3-3sigma. Mol Cancer Ther. 2006, 5 (4): 903-912. 10.1158/1535-7163.MCT-05-0393.CrossRefPubMed Han B, Xie H, Chen Q, Zhang JT: Sensitizing hormone-refractory prostate cancer cells to drug treatment by targeting 14-3-3sigma. Mol Cancer Ther. 2006, 5 (4): 903-912. 10.1158/1535-7163.MCT-05-0393.CrossRefPubMed
11.
go back to reference Friess H, Ding J, Kleeff J, Fenkell L, Rosinski JA, Guweidhi A, Reidhaar-Olson JF, Korc M, Hammer J, Buchler MW: Microarray-based identification of differentially expressed growth- and metastasis-associated genes in pancreatic cancer. Cell Mol Life Sci. 2003, 60 (6): 1180-1199.PubMed Friess H, Ding J, Kleeff J, Fenkell L, Rosinski JA, Guweidhi A, Reidhaar-Olson JF, Korc M, Hammer J, Buchler MW: Microarray-based identification of differentially expressed growth- and metastasis-associated genes in pancreatic cancer. Cell Mol Life Sci. 2003, 60 (6): 1180-1199.PubMed
12.
go back to reference Logsdon CD, Simeone DM, Binkley C, Arumugam T, Greenson JK, Giordano TJ, Misek DE, Kuick R, Hanash S: Molecular profiling of pancreatic adenocarcinoma and chronic pancreatitis identifies multiple genes differentially regulated in pancreatic cancer. Cancer Res. 2003, 63 (10): 2649-2657.PubMed Logsdon CD, Simeone DM, Binkley C, Arumugam T, Greenson JK, Giordano TJ, Misek DE, Kuick R, Hanash S: Molecular profiling of pancreatic adenocarcinoma and chronic pancreatitis identifies multiple genes differentially regulated in pancreatic cancer. Cancer Res. 2003, 63 (10): 2649-2657.PubMed
13.
go back to reference Iacobuzio-Donahue CA, Maitra A, Olsen M, Lowe AW, van Heek NT, Rosty C, Walter K, Sato N, Parker A, Ashfaq R, et al: Exploration of global gene expression patterns in pancreatic adenocarcinoma using cDNA microarrays. Am J Pathol. 2003, 162 (4): 1151-1162.CrossRefPubMedPubMedCentral Iacobuzio-Donahue CA, Maitra A, Olsen M, Lowe AW, van Heek NT, Rosty C, Walter K, Sato N, Parker A, Ashfaq R, et al: Exploration of global gene expression patterns in pancreatic adenocarcinoma using cDNA microarrays. Am J Pathol. 2003, 162 (4): 1151-1162.CrossRefPubMedPubMedCentral
14.
go back to reference Guweidhi A, Kleeff J, Giese N, Fitori JE, Ketterer K, Giese T, Buchler MW, Korc M, Friess H: Enhanced expression of 14-3-3sigma in pancreatic cancer and its role in cell cycle regulation and apoptosis. Carcinogenesis. 2004, 25 (9): 1575-1585. 10.1093/carcin/bgh159.CrossRefPubMed Guweidhi A, Kleeff J, Giese N, Fitori JE, Ketterer K, Giese T, Buchler MW, Korc M, Friess H: Enhanced expression of 14-3-3sigma in pancreatic cancer and its role in cell cycle regulation and apoptosis. Carcinogenesis. 2004, 25 (9): 1575-1585. 10.1093/carcin/bgh159.CrossRefPubMed
15.
go back to reference Liu Z, Dong Z, Yang Z, Chen Q, Pan Y, Yang Y, Cui P, Zhang X, Zhang JT: Role of eIF3a (eIF3 p170) in intestinal cell differentiation and its association with early development. Differentiation. 2007, 75 (7): 652-661. 10.1111/j.1432-0436.2007.00165.x.CrossRefPubMed Liu Z, Dong Z, Yang Z, Chen Q, Pan Y, Yang Y, Cui P, Zhang X, Zhang JT: Role of eIF3a (eIF3 p170) in intestinal cell differentiation and its association with early development. Differentiation. 2007, 75 (7): 652-661. 10.1111/j.1432-0436.2007.00165.x.CrossRefPubMed
16.
go back to reference Papazisis KT, Geromichalos GD, Dimitriadis KA, Kortsaris AH: Optimization of the sulforhodamine B colorimetric assay. J Immunol Methods. 1997, 208 (2): 151-158. 10.1016/S0022-1759(97)00137-3.CrossRefPubMed Papazisis KT, Geromichalos GD, Dimitriadis KA, Kortsaris AH: Optimization of the sulforhodamine B colorimetric assay. J Immunol Methods. 1997, 208 (2): 151-158. 10.1016/S0022-1759(97)00137-3.CrossRefPubMed
17.
go back to reference Xu J, Peng H, Chen Q, Liu Y, Dong Z, Zhang JT: Oligomerization domain of the multidrug resistance-associated transporter ABCG2 and its dominant inhibitory activity. Cancer Res. 2007, 67 (9): 4373-4381. 10.1158/0008-5472.CAN-06-3169.CrossRefPubMed Xu J, Peng H, Chen Q, Liu Y, Dong Z, Zhang JT: Oligomerization domain of the multidrug resistance-associated transporter ABCG2 and its dominant inhibitory activity. Cancer Res. 2007, 67 (9): 4373-4381. 10.1158/0008-5472.CAN-06-3169.CrossRefPubMed
18.
go back to reference Morgan MA, Meirovitz A, Davis MA, Kollar LE, Hassan MC, Lawrence TS: Radiotherapy combined with gemcitabine and oxaliplatin in pancreatic cancer cells. Transl Oncol. 2008, 1 (1): 36-43.CrossRefPubMedPubMedCentral Morgan MA, Meirovitz A, Davis MA, Kollar LE, Hassan MC, Lawrence TS: Radiotherapy combined with gemcitabine and oxaliplatin in pancreatic cancer cells. Transl Oncol. 2008, 1 (1): 36-43.CrossRefPubMedPubMedCentral
19.
go back to reference Ferguson AT, Evron E, Umbricht CB, Pandita TK, Chan TA, Hermeking H, Marks JR, Lambers AR, Futreal PA, Stampfer MR, et al: High frequency of hypermethylation at the 14-3-3 sigma locus leads to gene silencing in breast cancer. PNAS. 2000, 97 (11): 6049-6054. 10.1073/pnas.100566997.CrossRefPubMedPubMedCentral Ferguson AT, Evron E, Umbricht CB, Pandita TK, Chan TA, Hermeking H, Marks JR, Lambers AR, Futreal PA, Stampfer MR, et al: High frequency of hypermethylation at the 14-3-3 sigma locus leads to gene silencing in breast cancer. PNAS. 2000, 97 (11): 6049-6054. 10.1073/pnas.100566997.CrossRefPubMedPubMedCentral
20.
go back to reference Vercoutter-Edouart A-S, Lemoine J, Le Bourhis X, Louis H, Boilly B, Nurcombe V, Revillion F, Peyrat JP, Hondermarck H: Proteomic analysis reveals that 14-3-3sigma Is down-regulated in human breast cancer cells. Cancer Res. 2001, 61 (1): 76-80.PubMed Vercoutter-Edouart A-S, Lemoine J, Le Bourhis X, Louis H, Boilly B, Nurcombe V, Revillion F, Peyrat JP, Hondermarck H: Proteomic analysis reveals that 14-3-3sigma Is down-regulated in human breast cancer cells. Cancer Res. 2001, 61 (1): 76-80.PubMed
21.
go back to reference Iwata N, Yamamoto H, Sasaki S, Itoh F, Suzuki H, Kikuchi T, Kaneto H, Iku S, Ozeki I, Karino Y, et al: Frequent hypermethylation of CpG islands and loss of expression of the 14-3-3 sigma gene in human hepatocellular carcinoma. Oncogene. 2000, 19 (46): 5298-5302. 10.1038/sj.onc.1203898.CrossRefPubMed Iwata N, Yamamoto H, Sasaki S, Itoh F, Suzuki H, Kikuchi T, Kaneto H, Iku S, Ozeki I, Karino Y, et al: Frequent hypermethylation of CpG islands and loss of expression of the 14-3-3 sigma gene in human hepatocellular carcinoma. Oncogene. 2000, 19 (46): 5298-5302. 10.1038/sj.onc.1203898.CrossRefPubMed
22.
go back to reference Gasco M, Sullivan A, Repellin C, Brooks L, Farrell PJ, Tidy JA, Dunne B, Gusterson B, Evans DJ, Crook T: Coincident inactivation of 14-3-3sigma and p16INK4a is an early event in vulval squamous neoplasia. Oncogene. 2002, 21 (12): 1876-1881. 10.1038/sj.onc.1205256.CrossRefPubMed Gasco M, Sullivan A, Repellin C, Brooks L, Farrell PJ, Tidy JA, Dunne B, Gusterson B, Evans DJ, Crook T: Coincident inactivation of 14-3-3sigma and p16INK4a is an early event in vulval squamous neoplasia. Oncogene. 2002, 21 (12): 1876-1881. 10.1038/sj.onc.1205256.CrossRefPubMed
23.
go back to reference Gasco M, Bell AK, Heath V, Sullivan A, Smith P, Hiller L, Yulug I, Numico G, Merlano M, Farrell PJ, et al: Epigenetic inactivation of 14-3-3 sigma in oral carcinoma: association with p16(INK4a) silencing and human papillomavirus negativity. Cancer Res. 2002, 62 (7): 2072-2076.PubMed Gasco M, Bell AK, Heath V, Sullivan A, Smith P, Hiller L, Yulug I, Numico G, Merlano M, Farrell PJ, et al: Epigenetic inactivation of 14-3-3 sigma in oral carcinoma: association with p16(INK4a) silencing and human papillomavirus negativity. Cancer Res. 2002, 62 (7): 2072-2076.PubMed
24.
go back to reference Yatabe Y, Osada H, Tatematsu Y, Mitsudomi T, Takahashi T: Decreased expression of 14-3-3sigma in neuroendocrine tumors is independent of origin and malignant potential. Oncogene. 2002, 21 (54): 8310-8319. 10.1038/sj.onc.1206014.CrossRefPubMed Yatabe Y, Osada H, Tatematsu Y, Mitsudomi T, Takahashi T: Decreased expression of 14-3-3sigma in neuroendocrine tumors is independent of origin and malignant potential. Oncogene. 2002, 21 (54): 8310-8319. 10.1038/sj.onc.1206014.CrossRefPubMed
25.
go back to reference Osada H, Tatematsu Y, Yatabe Y, Nakagawa T, Konishi H, Harano T, Tezel E, Takada M, Takahashi T: Frequent and histological type-specific inactivation of 14-3-3sigma in human lung cancers. Oncogene. 2002, 21 (15): 2418-2424. 10.1038/sj.onc.1205303.CrossRefPubMed Osada H, Tatematsu Y, Yatabe Y, Nakagawa T, Konishi H, Harano T, Tezel E, Takada M, Takahashi T: Frequent and histological type-specific inactivation of 14-3-3sigma in human lung cancers. Oncogene. 2002, 21 (15): 2418-2424. 10.1038/sj.onc.1205303.CrossRefPubMed
26.
go back to reference Liu Y, Chen Q, Zhang JT: Tumor suppressor gene 14-3-3sigma is down-regulated whereas the proto-oncogene translation elongation factor 1delta is up-regulated in non-small cell lung cancers as identified by proteomic profiling. J Proteome Res. 2004, 3 (4): 728-735. 10.1021/pr034127+.CrossRefPubMed Liu Y, Chen Q, Zhang JT: Tumor suppressor gene 14-3-3sigma is down-regulated whereas the proto-oncogene translation elongation factor 1delta is up-regulated in non-small cell lung cancers as identified by proteomic profiling. J Proteome Res. 2004, 3 (4): 728-735. 10.1021/pr034127+.CrossRefPubMed
27.
go back to reference Suzuki H, Itoh F, Toyota M, Kikuchi T, Kakiuchi H, Imai K: Inactivation of the 14-3-3sigma Gene Is Associated with 5' CpG Island Hypermethylation in Human Cancers. Cancer Res. 2000, 60 (16): 4353-4357.PubMed Suzuki H, Itoh F, Toyota M, Kikuchi T, Kakiuchi H, Imai K: Inactivation of the 14-3-3sigma Gene Is Associated with 5' CpG Island Hypermethylation in Human Cancers. Cancer Res. 2000, 60 (16): 4353-4357.PubMed
28.
go back to reference Umbricht CB, Evron E, Gabrielson E, Ferguson A, Marks J, Sukumar S: Hypermethylation of 14-3-3 sigma (stratifin) is an early event in breast cancer. Oncogene. 2001, 20 (26): 3348-3353. 10.1038/sj.onc.1204438.CrossRefPubMed Umbricht CB, Evron E, Gabrielson E, Ferguson A, Marks J, Sukumar S: Hypermethylation of 14-3-3 sigma (stratifin) is an early event in breast cancer. Oncogene. 2001, 20 (26): 3348-3353. 10.1038/sj.onc.1204438.CrossRefPubMed
29.
go back to reference Benzinger A, Muster N, Koch HB, Yates JR, Hermeking H: Targeted proteomic analysis of 14-3-3sigma, a p53 effector commonly silenced in cancer. Mol Cell Proteomics. 2005, 4 (6): 785-795. 10.1074/mcp.M500021-MCP200. 3CrossRefPubMed Benzinger A, Muster N, Koch HB, Yates JR, Hermeking H: Targeted proteomic analysis of 14-3-3sigma, a p53 effector commonly silenced in cancer. Mol Cell Proteomics. 2005, 4 (6): 785-795. 10.1074/mcp.M500021-MCP200. 3CrossRefPubMed
30.
go back to reference Simpson PT, Gale T, Reis-Filho JS, Jones C, Parry S, Steele D, Cossu A, Budroni M, Palmieri G, Lakhani SR: Distribution and significance of 14-3-3sigma, a novel myoepithelial marker, in normal, benign, and malignant breast tissue. J Pathol. 2004, 202 (3): 274-285. 10.1002/path.1530.CrossRefPubMed Simpson PT, Gale T, Reis-Filho JS, Jones C, Parry S, Steele D, Cossu A, Budroni M, Palmieri G, Lakhani SR: Distribution and significance of 14-3-3sigma, a novel myoepithelial marker, in normal, benign, and malignant breast tissue. J Pathol. 2004, 202 (3): 274-285. 10.1002/path.1530.CrossRefPubMed
31.
go back to reference Nakanishi K, Hashizume S, Kato M, Honjoh T, Setoguchi Y, Yasumoto K: Elevated expression levels of the 14-3-3 family of proteins in lung cancer tissues. Hum Antibodies. 1997, 8 (4): 189-194.PubMed Nakanishi K, Hashizume S, Kato M, Honjoh T, Setoguchi Y, Yasumoto K: Elevated expression levels of the 14-3-3 family of proteins in lung cancer tissues. Hum Antibodies. 1997, 8 (4): 189-194.PubMed
32.
go back to reference Villaret DB, Wang T, Dillon D, Xu J, Sivam D, Cheever MA, Reed SG: Identification of genes overexpressed in head and neck squamous cell carcinoma using a combination of complementary DNA subtraction and microarray analysis. Laryngoscope. 2000, 110 (3 Pt 1): 374-381. 10.1097/00005537-200003000-00008.CrossRefPubMed Villaret DB, Wang T, Dillon D, Xu J, Sivam D, Cheever MA, Reed SG: Identification of genes overexpressed in head and neck squamous cell carcinoma using a combination of complementary DNA subtraction and microarray analysis. Laryngoscope. 2000, 110 (3 Pt 1): 374-381. 10.1097/00005537-200003000-00008.CrossRefPubMed
33.
go back to reference Neupane D, Korc M: 14-3-3sigma modulates pancreatic cancer cell survival and invasiveness. Clin Cancer Res. 2008, 14 (23): 7614-7623. 10.1158/1078-0432.CCR-08-1366.CrossRefPubMedPubMedCentral Neupane D, Korc M: 14-3-3sigma modulates pancreatic cancer cell survival and invasiveness. Clin Cancer Res. 2008, 14 (23): 7614-7623. 10.1158/1078-0432.CCR-08-1366.CrossRefPubMedPubMedCentral
34.
go back to reference Hustinx SR, Fukushima N, Zahurak ML, Riall TS, Maitra A, Brosens L, Cameron JL, Yeo CJ, Offerhaus GJ, Hruban RH, et al: Expression and prognostic significance of 14-3-3sigma and ERM family protein expression in periampullary neoplasms. Cancer Biol Ther. 2005, 4 (5): 596-601. 10.4161/cbt.4.5.1748.CrossRefPubMed Hustinx SR, Fukushima N, Zahurak ML, Riall TS, Maitra A, Brosens L, Cameron JL, Yeo CJ, Offerhaus GJ, Hruban RH, et al: Expression and prognostic significance of 14-3-3sigma and ERM family protein expression in periampullary neoplasms. Cancer Biol Ther. 2005, 4 (5): 596-601. 10.4161/cbt.4.5.1748.CrossRefPubMed
35.
go back to reference Urano T, Saito T, Tsukui T, Fujita M, Hosoi T, Muramatsu M, Ouchi Y, Inoue S: Efp targets 14-3-3 sigma for proteolysis and promotes breast tumour growth. Nature. 2002, 417 (6891): 871-875. 10.1038/nature00826.CrossRefPubMed Urano T, Saito T, Tsukui T, Fujita M, Hosoi T, Muramatsu M, Ouchi Y, Inoue S: Efp targets 14-3-3 sigma for proteolysis and promotes breast tumour growth. Nature. 2002, 417 (6891): 871-875. 10.1038/nature00826.CrossRefPubMed
36.
go back to reference Suzuki T, Urano T, Miki Y, Moriya T, Akahira J, Ishida T, Horie K, Inoue S, Sasano H: Nuclear cyclin B1 in human breast carcinoma as a potent prognostic factor. Cancer Sci. 2007, 98 (5): 644-651. 10.1111/j.1349-7006.2007.00444.x.CrossRefPubMed Suzuki T, Urano T, Miki Y, Moriya T, Akahira J, Ishida T, Horie K, Inoue S, Sasano H: Nuclear cyclin B1 in human breast carcinoma as a potent prognostic factor. Cancer Sci. 2007, 98 (5): 644-651. 10.1111/j.1349-7006.2007.00444.x.CrossRefPubMed
37.
go back to reference Perathoner A, Pirkebner D, Brandacher G, Spizzo G, Stadlmann S, Obrist P, Margreiter R, Amberger A: 14-3-3sigma expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients. Clin Cancer Res. 2005, 11 (9): 3274-3279. 10.1158/1078-0432.CCR-04-2207.CrossRefPubMed Perathoner A, Pirkebner D, Brandacher G, Spizzo G, Stadlmann S, Obrist P, Margreiter R, Amberger A: 14-3-3sigma expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients. Clin Cancer Res. 2005, 11 (9): 3274-3279. 10.1158/1078-0432.CCR-04-2207.CrossRefPubMed
38.
go back to reference Cheng L, Pan CX, Zhang JT, Zhang S, Kinch MS, Li L, Baldridge LA, Wade C, Hu Z, Koch MO, et al: Loss of 14-3-3sigma in prostate cancer and its precursors. Clin Cancer Res. 2004, 10 (9): 3064-3068. 10.1158/1078-0432.CCR-03-0652.CrossRefPubMed Cheng L, Pan CX, Zhang JT, Zhang S, Kinch MS, Li L, Baldridge LA, Wade C, Hu Z, Koch MO, et al: Loss of 14-3-3sigma in prostate cancer and its precursors. Clin Cancer Res. 2004, 10 (9): 3064-3068. 10.1158/1078-0432.CCR-03-0652.CrossRefPubMed
39.
go back to reference Ito K, Suzuki T, Akahira J, Sakuma M, Saitou S, Okamoto S, Niikura H, Okamura K, Yaegashi N, Sasano H, et al: 14-3-3sigma in endometrial cancer--a possible prognostic marker in early-stage cancer. Clin Cancer Res. 2005, 11 (20): 7384-7391. 10.1158/1078-0432.CCR-05-0187.CrossRefPubMed Ito K, Suzuki T, Akahira J, Sakuma M, Saitou S, Okamoto S, Niikura H, Okamura K, Yaegashi N, Sasano H, et al: 14-3-3sigma in endometrial cancer--a possible prognostic marker in early-stage cancer. Clin Cancer Res. 2005, 11 (20): 7384-7391. 10.1158/1078-0432.CCR-05-0187.CrossRefPubMed
40.
go back to reference Erovic BM, Pelzmann M, Grasl M, Pammer J, Kornek G, Brannath W, Selzer E, Thurnher D: Mcl-1, vascular endothelial growth factor-R2, and 14-3-3sigma expression might predict primary response against radiotherapy and chemotherapy in patients with locally advanced squamous cell carcinomas of the head and neck. Clin Cancer Res. 2005, 11 (24 Pt 1): 8632-8636. 10.1158/1078-0432.CCR-05-1170.CrossRefPubMed Erovic BM, Pelzmann M, Grasl M, Pammer J, Kornek G, Brannath W, Selzer E, Thurnher D: Mcl-1, vascular endothelial growth factor-R2, and 14-3-3sigma expression might predict primary response against radiotherapy and chemotherapy in patients with locally advanced squamous cell carcinomas of the head and neck. Clin Cancer Res. 2005, 11 (24 Pt 1): 8632-8636. 10.1158/1078-0432.CCR-05-1170.CrossRefPubMed
41.
go back to reference Ramirez JL, Rosell R, Taron M, Sanchez-Ronco M, Alberola V, de Las Penas R, Sanchez JM, Moran T, Camps C, Massuti B, et al: 14-3-3sigma methylation in pretreatment serum circulating DNA of cisplatin-plus-gemcitabine-treated advanced non-small-cell lung cancer patients predicts survival: The Spanish Lung Cancer Group. J Clin Oncol. 2005, 23 (36): 9105-9112. 10.1200/JCO.2005.02.2905.CrossRefPubMed Ramirez JL, Rosell R, Taron M, Sanchez-Ronco M, Alberola V, de Las Penas R, Sanchez JM, Moran T, Camps C, Massuti B, et al: 14-3-3sigma methylation in pretreatment serum circulating DNA of cisplatin-plus-gemcitabine-treated advanced non-small-cell lung cancer patients predicts survival: The Spanish Lung Cancer Group. J Clin Oncol. 2005, 23 (36): 9105-9112. 10.1200/JCO.2005.02.2905.CrossRefPubMed
42.
go back to reference Cheng AL, Huang WG, Chen ZC, Peng F, Zhang PF, Li MY, Li F, Li JL, Li C, Yi H, et al: Identification of Novel Nasopharyngeal Carcinoma Biomarkers by Laser Capture Microdissection and Proteomic Analysis. Clin Cancer Res. 2008, 14 (2): 435-445. 10.1158/1078-0432.CCR-07-1215.CrossRefPubMed Cheng AL, Huang WG, Chen ZC, Peng F, Zhang PF, Li MY, Li F, Li JL, Li C, Yi H, et al: Identification of Novel Nasopharyngeal Carcinoma Biomarkers by Laser Capture Microdissection and Proteomic Analysis. Clin Cancer Res. 2008, 14 (2): 435-445. 10.1158/1078-0432.CCR-07-1215.CrossRefPubMed
43.
go back to reference Chan TA, Hermeking H, Lengauer C, Kinzler KW, Vogelstein B: 14-3-3Sigma is required to prevent mitotic catastrophe after DNA damage. Nature. 1999, 401 (6753): 616-620. 10.1038/44188.CrossRefPubMed Chan TA, Hermeking H, Lengauer C, Kinzler KW, Vogelstein B: 14-3-3Sigma is required to prevent mitotic catastrophe after DNA damage. Nature. 1999, 401 (6753): 616-620. 10.1038/44188.CrossRefPubMed
44.
go back to reference Samuel T, Weber HO, Rauch P, Verdoodt B, Eppel JT, McShea A, Hermeking H, Funk JO: The G2/M regulator 14-3-3sigma prevents apoptosis through sequestration of Bax. J Biol Chem. 2001, 276 (48): 45201-45206. 10.1074/jbc.M106427200.CrossRefPubMed Samuel T, Weber HO, Rauch P, Verdoodt B, Eppel JT, McShea A, Hermeking H, Funk JO: The G2/M regulator 14-3-3sigma prevents apoptosis through sequestration of Bax. J Biol Chem. 2001, 276 (48): 45201-45206. 10.1074/jbc.M106427200.CrossRefPubMed
Metadata
Title
Role of 14-3-3σ in poor prognosis and in radiation and drug resistance of human pancreatic cancers
Authors
Zhaomin Li
Zizheng Dong
David Myer
Michele Yip-Schneider
Jianguo Liu
Ping Cui
C Max Schmidt
Jian-Ting Zhang
Publication date
01-12-2010
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2010
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/1471-2407-10-598

Other articles of this Issue 1/2010

BMC Cancer 1/2010 Go to the issue
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