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Published in: Cancer and Metastasis Reviews 3-4/2013

01-12-2013 | NON-THEMATIC REVIEW

Role of the host stroma in cancer and its therapeutic significance

Author: David Tarin

Published in: Cancer and Metastasis Reviews | Issue 3-4/2013

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Abstract

Current cancer research focuses mainly upon the cancer cells in malignant tumours and is providing a growing database about aberrations in their genetic composition. However, tumours also contain non-cancerous host tissue, referred to as the stroma, which plays an active and indispensable role in tumour growth and influences the virulence of the neoplasm towards the host. Many cell types inhabit the stroma, amidst apparently inert fibrous and viscous matrix material, composed of complex polysaccharides, proteins and other molecules. Actually, all of these elements are in constant turnover, causing unpredictable evolution in the properties of the community. This article provides pathologic observations and data on reciprocal interactions between these stromal and neoplastic components of tumours and how they change during the course of the disease. Malignant progression depends upon dauntingly intricate communications between different specialised lineages within the cellular society, which enable rapid adaptation to changing circumstances. Opportunistic misuse of such communication networks enables tumour cells to recruit and incorporate adjacent normal stroma into their midst, so that they may grow, infiltrate and parasitise the host. The absolute dependency of primary tumours and metastases on their diverse stromal components for survival and their insatiable need to continuously recruit more stroma to support expansion, renders them vulnerable to strategies capable of disrupting the cellular interactions involved. This dependency is of critical importance for cancer therapy research, and proposed methods for turning this parasitic behaviour of tumours against themselves are suggested below.
Literature
1.
go back to reference Folkman, J. (2006). Angiogenesis. Annual Review of Medicine, 57, 1–18.PubMed Folkman, J. (2006). Angiogenesis. Annual Review of Medicine, 57, 1–18.PubMed
2.
go back to reference Yamagiwa, K., Ichikawa, K., cited by Yamagiwa KaI, K. (1918). Experimental study of the pathogenesis of carcinoma. Journal of Cancer Research 3, 1–29. Yamagiwa, K., Ichikawa, K., cited by Yamagiwa KaI, K. (1918). Experimental study of the pathogenesis of carcinoma. Journal of Cancer Research 3, 1–29.
3.
go back to reference Orr, J. W. (1938). The changes antecedent to tumour formation during the treatment of mouse skin with carcinogenic hydrocarbons. Journal of Pathology and Bacteriology, 46, 495–515. Orr, J. W. (1938). The changes antecedent to tumour formation during the treatment of mouse skin with carcinogenic hydrocarbons. Journal of Pathology and Bacteriology, 46, 495–515.
4.
go back to reference Billingham, R. E., Orr, J. W., & Woodhouse, D. L. (1951). Transplantation od skin components during chemical carcinogenesis with 20-methylcholanthrene. British Journal of Cancer, 5, 417–432.PubMed Billingham, R. E., Orr, J. W., & Woodhouse, D. L. (1951). Transplantation od skin components during chemical carcinogenesis with 20-methylcholanthrene. British Journal of Cancer, 5, 417–432.PubMed
5.
go back to reference Marchant, J., & Orr, J. W. (1953). Further attempts to analyse the role of epidermis and deeper tissues in experimental chemical carcinogenesis by transplantation and other method. British Journal of Cancer, 7, 329–341.PubMed Marchant, J., & Orr, J. W. (1953). Further attempts to analyse the role of epidermis and deeper tissues in experimental chemical carcinogenesis by transplantation and other method. British Journal of Cancer, 7, 329–341.PubMed
6.
go back to reference Orr, J. W., & Spencer, A. T. (1972). Transplantation studies of the role of the stroma in epidermal carcinogenesis. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 291–303). London: Academic. Orr, J. W., & Spencer, A. T. (1972). Transplantation studies of the role of the stroma in epidermal carcinogenesis. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 291–303). London: Academic.
7.
go back to reference Tarin, D. (2012). Inappropriate gene expression in human cancer and its far-reaching biological and clinical significance. Cancer Metastasis Reviews, 31, 21–39.PubMed Tarin, D. (2012). Inappropriate gene expression in human cancer and its far-reaching biological and clinical significance. Cancer Metastasis Reviews, 31, 21–39.PubMed
8.
go back to reference Pelosof, L. C., & Gerber, D. E. (2010). Paraneoplastic syndromes: an approach to diagnosis and treatment. Mayo Clinic Proceedings Mayo Clinic, 85, 838–854.PubMed Pelosof, L. C., & Gerber, D. E. (2010). Paraneoplastic syndromes: an approach to diagnosis and treatment. Mayo Clinic Proceedings Mayo Clinic, 85, 838–854.PubMed
9.
go back to reference Darnell, R., & Posner, J. (2011). Paraneoplastic syndromes. Oxford: Oxford University Press. Darnell, R., & Posner, J. (2011). Paraneoplastic syndromes. Oxford: Oxford University Press.
10.
go back to reference Spemann, H. (1938). Embryonic development and induction. New Haven: Yale University Press. Spemann, H. (1938). Embryonic development and induction. New Haven: Yale University Press.
11.
go back to reference Grobstein, C. (1967). Mechanisms of organogenetic tissue interaction. National Cancer Institute Monograph, 26, 279–299.PubMed Grobstein, C. (1967). Mechanisms of organogenetic tissue interaction. National Cancer Institute Monograph, 26, 279–299.PubMed
12.
go back to reference Saxén, L. (1972). Interactive mechanisms in morphogenesis. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 49–80). London: Academic. Saxén, L. (1972). Interactive mechanisms in morphogenesis. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 49–80). London: Academic.
14.
go back to reference Franks, T. J., Colby, T. V., Travis, W. D., et al. (2008). Resident cellular components of the human lung: current knowledge and goals for research on cell phenotyping and function. Proceedings of the American Thoracic Society, 5, 763–766.PubMed Franks, T. J., Colby, T. V., Travis, W. D., et al. (2008). Resident cellular components of the human lung: current knowledge and goals for research on cell phenotyping and function. Proceedings of the American Thoracic Society, 5, 763–766.PubMed
15.
go back to reference Beers, M. F., & Morrisey, E. E. (2011). The three R’s of lung health and disease: repair, remodeling, and regeneration. The Journal of Clinical Investigation, 121, 2065–2073.PubMed Beers, M. F., & Morrisey, E. E. (2011). The three R’s of lung health and disease: repair, remodeling, and regeneration. The Journal of Clinical Investigation, 121, 2065–2073.PubMed
16.
go back to reference Cardoso, W. V., & Lu, J. (2006). Regulation of early lung morphogenesis: questions, facts and controversies. Development, 133, 1611–1624.PubMed Cardoso, W. V., & Lu, J. (2006). Regulation of early lung morphogenesis: questions, facts and controversies. Development, 133, 1611–1624.PubMed
17.
go back to reference Cardoso, W. V., & Whitsett, J. A. (2008). Resident cellular components of the lung: developmental aspects. Proceedings of the American Thoracic Society, 5, 767–771.PubMed Cardoso, W. V., & Whitsett, J. A. (2008). Resident cellular components of the lung: developmental aspects. Proceedings of the American Thoracic Society, 5, 767–771.PubMed
18.
go back to reference Grobstein, C. (1953). Morphogenetic interaction between embryonic mouse tissues separated by a membrane filter. Nature, 172, 869–870.PubMed Grobstein, C. (1953). Morphogenetic interaction between embryonic mouse tissues separated by a membrane filter. Nature, 172, 869–870.PubMed
19.
go back to reference Kratochwil, K. (1972). Tissue interaction during embryonic development. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 1–47). London: Academic. Kratochwil, K. (1972). Tissue interaction during embryonic development. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 1–47). London: Academic.
20.
go back to reference Millar, S. E. (2002). Molecular mechanisms regulating hair follicle development. The Journal of Investigative Dermatology, 118, 216–225.PubMed Millar, S. E. (2002). Molecular mechanisms regulating hair follicle development. The Journal of Investigative Dermatology, 118, 216–225.PubMed
22.
go back to reference Landsman, L., Nijagal, A., Whitchurch, T. J., et al. (2011). Pancreatic mesenchyme regulates epithelial organogenesis throughout development. PLoS Biology, 9, e1001143.PubMed Landsman, L., Nijagal, A., Whitchurch, T. J., et al. (2011). Pancreatic mesenchyme regulates epithelial organogenesis throughout development. PLoS Biology, 9, e1001143.PubMed
23.
go back to reference Tabin, C., & Wolpert, L. (2007). Rethinking the proximodistal axis of the vertebrate limb in the molecular era. Genes & Development, 21, 1433–1442. Tabin, C., & Wolpert, L. (2007). Rethinking the proximodistal axis of the vertebrate limb in the molecular era. Genes & Development, 21, 1433–1442.
24.
go back to reference Hölldobler, B., & Wilson, E. (2008). The superorganism: the beauty, elegance, and strangeness of insect societies. New York: W.W. Norton Inc. Hölldobler, B., & Wilson, E. (2008). The superorganism: the beauty, elegance, and strangeness of insect societies. New York: W.W. Norton Inc.
25.
go back to reference Corning, P. (2002). The re-emergence of emergence: a venerable concept in search of a theory. Complexity, 7, 18–30. Corning, P. (2002). The re-emergence of emergence: a venerable concept in search of a theory. Complexity, 7, 18–30.
26.
go back to reference Arp, R. (2008). Life and the homeostatic organization view of biological phenomena. Cosmos and History: The Journal of Natural and Social Philosophy, 4, 260–282. Arp, R. (2008). Life and the homeostatic organization view of biological phenomena. Cosmos and History: The Journal of Natural and Social Philosophy, 4, 260–282.
27.
go back to reference Tarin, D. (2011). Cell and tissue interactions in carcinogenesis and metastasis and their clinical significance. Seminars in Cancer Biology, 21, 72–82.PubMed Tarin, D. (2011). Cell and tissue interactions in carcinogenesis and metastasis and their clinical significance. Seminars in Cancer Biology, 21, 72–82.PubMed
28.
go back to reference Meilhac, S. M., Adams, R. J., Morris, S. A., et al. (2009). Active cell movements coupled to positional induction are involved in lineage segregation in the mouse blastocyst. Developmental Biology, 331, 210–221.PubMed Meilhac, S. M., Adams, R. J., Morris, S. A., et al. (2009). Active cell movements coupled to positional induction are involved in lineage segregation in the mouse blastocyst. Developmental Biology, 331, 210–221.PubMed
29.
go back to reference Rinn, J. L., Bondre, C., Gladstone, H. B., et al. (2006). Anatomic demarcation by positional variation in fibroblast gene expression programs. PLoS Genetics, 2, e119.PubMed Rinn, J. L., Bondre, C., Gladstone, H. B., et al. (2006). Anatomic demarcation by positional variation in fibroblast gene expression programs. PLoS Genetics, 2, e119.PubMed
30.
go back to reference Shannon, J. M., & Hyatt, B. A. (2004). Epithelial–mesenchymal interactions in the developing lung. Annual Review of Physiology, 66, 625–645.PubMed Shannon, J. M., & Hyatt, B. A. (2004). Epithelial–mesenchymal interactions in the developing lung. Annual Review of Physiology, 66, 625–645.PubMed
31.
go back to reference Billingham, R. E., & Silvers, W. K. (1963). The origin and conservation of epidermal specificities. The New England Journal of Medicine, 268, 539–545. concl.PubMed Billingham, R. E., & Silvers, W. K. (1963). The origin and conservation of epidermal specificities. The New England Journal of Medicine, 268, 539–545. concl.PubMed
32.
go back to reference Billingham, R., & Silvers, W. (1968). Dermoepidermal interactions and epithelial specificity. In R. Fleischmajer & R. Billingham (Eds.), Epithelial–mesenchymal interactions (pp. 252–266). Baltimore: Williams and Wilkins. Billingham, R., & Silvers, W. (1968). Dermoepidermal interactions and epithelial specificity. In R. Fleischmajer & R. Billingham (Eds.), Epithelial–mesenchymal interactions (pp. 252–266). Baltimore: Williams and Wilkins.
33.
go back to reference Cunha, G. R., Fujii, H., Neubauer, B. L., et al. (1983). Epithelial–mesenchymal interactions in prostatic development. I. Morphological observations of prostatic induction by urogenital sinus mesenchyme in epithelium of the adult rodent urinary bladder. The Journal of Cell Biology, 96, 1662–1670.PubMed Cunha, G. R., Fujii, H., Neubauer, B. L., et al. (1983). Epithelial–mesenchymal interactions in prostatic development. I. Morphological observations of prostatic induction by urogenital sinus mesenchyme in epithelium of the adult rodent urinary bladder. The Journal of Cell Biology, 96, 1662–1670.PubMed
34.
go back to reference Cunha, G. R., Hayward, S. W., & Wang, Y. Z. (2002). Role of stroma in carcinogenesis of the prostate. Differentiation, 70, 473–485.PubMed Cunha, G. R., Hayward, S. W., & Wang, Y. Z. (2002). Role of stroma in carcinogenesis of the prostate. Differentiation, 70, 473–485.PubMed
35.
go back to reference Dawe, C. (1972). Epithelial–mesenchymal interactions in relation to the genesis of polyoma virus-induced tumors of mouse salivary gland. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 305–358). London: Academic. Dawe, C. (1972). Epithelial–mesenchymal interactions in relation to the genesis of polyoma virus-induced tumors of mouse salivary gland. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 305–358). London: Academic.
36.
go back to reference Tarin, D., Price, J. E., Kettlewell, M. G., et al. (1984). Mechanisms of human tumor metastasis studied in patients with peritoneovenous shunts. Cancer Research, 44, 3584–3592.PubMed Tarin, D., Price, J. E., Kettlewell, M. G., et al. (1984). Mechanisms of human tumor metastasis studied in patients with peritoneovenous shunts. Cancer Research, 44, 3584–3592.PubMed
37.
go back to reference Suzuki, M., Mose, E. S., Montel, V., et al. (2006). Dormant cancer cells retrieved from metastasis-free organs regain tumorigenic and metastatic potency. The American Journal of Pathology, 169, 673–681.PubMed Suzuki, M., Mose, E. S., Montel, V., et al. (2006). Dormant cancer cells retrieved from metastasis-free organs regain tumorigenic and metastatic potency. The American Journal of Pathology, 169, 673–681.PubMed
38.
go back to reference Paget, S. (1889). The distribution of secondary growths in cancer of the breast. The Lancet, i, 571–573. Paget, S. (1889). The distribution of secondary growths in cancer of the breast. The Lancet, i, 571–573.
39.
go back to reference Hart, I. R., & Fidler, I. J. (1980). Role of organ selectivity in the determination of metastatic patterns of B16 melanoma. Cancer Research, 40, 2281–2287.PubMed Hart, I. R., & Fidler, I. J. (1980). Role of organ selectivity in the determination of metastatic patterns of B16 melanoma. Cancer Research, 40, 2281–2287.PubMed
40.
go back to reference Goodison, S., Kawai, K., Hihara, J., et al. (2003). Prolonged dormancy and site-specific growth potential of cancer cells spontaneously disseminated from nonmetastatic breast tumors as revealed by labeling with green fluorescent protein. Clinical Cancer Research, 9, 3808–3814.PubMed Goodison, S., Kawai, K., Hihara, J., et al. (2003). Prolonged dormancy and site-specific growth potential of cancer cells spontaneously disseminated from nonmetastatic breast tumors as revealed by labeling with green fluorescent protein. Clinical Cancer Research, 9, 3808–3814.PubMed
41.
go back to reference Bresalier, R. S., Raper, S. E., Hujanen, E. S., et al. (1987). A new animal model for human colon cancer metastasis. International Journal of Cancer, 39, 625–630. Bresalier, R. S., Raper, S. E., Hujanen, E. S., et al. (1987). A new animal model for human colon cancer metastasis. International Journal of Cancer, 39, 625–630.
42.
go back to reference Morikawa, K., Walker, S. M., Nakajima, M., et al. (1988). Influence of organ environment on the growth, selection, and metastasis of human colon carcinoma cells in nude mice. Cancer Research, 48, 6863–6871.PubMed Morikawa, K., Walker, S. M., Nakajima, M., et al. (1988). Influence of organ environment on the growth, selection, and metastasis of human colon carcinoma cells in nude mice. Cancer Research, 48, 6863–6871.PubMed
43.
go back to reference Naito, S., von Eschenbach, A. C., Giavazzi, R., et al. (1986). Growth and metastasis of tumor cells isolated from a human renal cell carcinoma implanted into different organs of nude mice. Cancer Research, 46, 4109–4115.PubMed Naito, S., von Eschenbach, A. C., Giavazzi, R., et al. (1986). Growth and metastasis of tumor cells isolated from a human renal cell carcinoma implanted into different organs of nude mice. Cancer Research, 46, 4109–4115.PubMed
44.
go back to reference Stephenson, R. A., Dinney, C. P., Gohji, K., et al. (1992). Metastatic model for human prostate cancer using orthotopic implantation in nude mice. Journal of the National Cancer Institute, 84, 951–957.PubMed Stephenson, R. A., Dinney, C. P., Gohji, K., et al. (1992). Metastatic model for human prostate cancer using orthotopic implantation in nude mice. Journal of the National Cancer Institute, 84, 951–957.PubMed
45.
go back to reference Montel, V., Mose, E. S., & Tarin, D. (2006). Tumor–stromal interactions reciprocally modulate gene expression patterns during carcinogenesis and metastasis. International Journal of Cancer Journal International du Cancer, 119, 251–263.PubMed Montel, V., Mose, E. S., & Tarin, D. (2006). Tumor–stromal interactions reciprocally modulate gene expression patterns during carcinogenesis and metastasis. International Journal of Cancer Journal International du Cancer, 119, 251–263.PubMed
46.
go back to reference Bao, L., Pigott, R., Matsumura, Y., et al. (1993). Correlation of VLA-4 integrin expression with metastatic potential in various human tumour cell lines. Differentiation, 52, 239–246.PubMed Bao, L., Pigott, R., Matsumura, Y., et al. (1993). Correlation of VLA-4 integrin expression with metastatic potential in various human tumour cell lines. Differentiation, 52, 239–246.PubMed
47.
go back to reference Tarin, D., & Croft, C. B. (1970). Ultrastructural studies of wound healing in mouse skin. II. Dermo-epidermal interrelationships. Journal of Anatomy, 106, 79–91.PubMed Tarin, D., & Croft, C. B. (1970). Ultrastructural studies of wound healing in mouse skin. II. Dermo-epidermal interrelationships. Journal of Anatomy, 106, 79–91.PubMed
48.
go back to reference Croft, C. B., & Tarin, D. (1970). Ultrastructural studies of wound healing in mouse skin. I. Epithelial behaviour. Journal of Anatomy, 106, 63–77.PubMed Croft, C. B., & Tarin, D. (1970). Ultrastructural studies of wound healing in mouse skin. I. Epithelial behaviour. Journal of Anatomy, 106, 63–77.PubMed
49.
go back to reference Cowell, T. (1972). Control of epithelial invasion by connective tissue during embedding of the mouse ovum. In D. Tarin (Ed.), Tissue interactions in carcinogenesis. London: Academic. Cowell, T. (1972). Control of epithelial invasion by connective tissue during embedding of the mouse ovum. In D. Tarin (Ed.), Tissue interactions in carcinogenesis. London: Academic.
50.
go back to reference Konijeti, R., Rajfer, J., & Askari, A. (2009). Placenta percreta and the urologist. Reviews in Urology, 11, 173–176.PubMed Konijeti, R., Rajfer, J., & Askari, A. (2009). Placenta percreta and the urologist. Reviews in Urology, 11, 173–176.PubMed
51.
go back to reference Tarin, D. (1968). Further electron microscopic studies on the mechanism of carcinogenesis: the specificity of the changes in carcinogen-treated mouse skin. International Journal of Cancer Journal International du Cancer, 3, 734–742.PubMed Tarin, D. (1968). Further electron microscopic studies on the mechanism of carcinogenesis: the specificity of the changes in carcinogen-treated mouse skin. International Journal of Cancer Journal International du Cancer, 3, 734–742.PubMed
52.
go back to reference Tarin, D. (1969). Fine structure of murine mammary tumours: the relationship between epithelium and connective tissue in neoplasms induced by various agents. British Journal of Cancer, 23, 417–425.PubMed Tarin, D. (1969). Fine structure of murine mammary tumours: the relationship between epithelium and connective tissue in neoplasms induced by various agents. British Journal of Cancer, 23, 417–425.PubMed
53.
go back to reference Tarin, D. (1972). Morphological studies on the mechanism of carcinogenesis. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 227–289). London: Academic. Tarin, D. (1972). Morphological studies on the mechanism of carcinogenesis. In D. Tarin (Ed.), Tissue interactions in carcinogenesis (pp. 227–289). London: Academic.
54.
go back to reference Brand, K. G., Buoen, L. C., Johnson, K. H., et al. (1975). Etiological factors, stages, and the role of the foreign body in foreign body tumorigenesis: a review. Cancer Research, 35, 279–286.PubMed Brand, K. G., Buoen, L. C., Johnson, K. H., et al. (1975). Etiological factors, stages, and the role of the foreign body in foreign body tumorigenesis: a review. Cancer Research, 35, 279–286.PubMed
55.
go back to reference Buoen, L. C., Brand, I., & Brand, K. G. (1975). Foreign-body tumorigenesis: in vitro isolation and expansion of preneoplastic clonal cell populations. Journal of the National Cancer Institute, 55, 721–723.PubMed Buoen, L. C., Brand, I., & Brand, K. G. (1975). Foreign-body tumorigenesis: in vitro isolation and expansion of preneoplastic clonal cell populations. Journal of the National Cancer Institute, 55, 721–723.PubMed
56.
go back to reference Karp, R. D., Johnson, K. H., Buoen, L. C., et al. (1973). Tumorigenesis by Millipore filters in mice: histology and ultrastructure of tissue reactions as related to pore size. Journal of the National Cancer Institute, 51, 1275–1285.PubMed Karp, R. D., Johnson, K. H., Buoen, L. C., et al. (1973). Tumorigenesis by Millipore filters in mice: histology and ultrastructure of tissue reactions as related to pore size. Journal of the National Cancer Institute, 51, 1275–1285.PubMed
57.
go back to reference Tarin, D. (2012). Clinical and biological implications of the tumor microenvironment. Cancer Microenvironment, 5, 95–112. Tarin, D. (2012). Clinical and biological implications of the tumor microenvironment. Cancer Microenvironment, 5, 95–112.
58.
go back to reference Thiery, J. P. (2002). Epithelial–mesenchymal transitions in tumour progression. Nature Reviews. Cancer, 2, 442–454.PubMed Thiery, J. P. (2002). Epithelial–mesenchymal transitions in tumour progression. Nature Reviews. Cancer, 2, 442–454.PubMed
59.
go back to reference Kalluri, R., & Weinberg, R. A. (2009). The basics of epithelial–mesenchymal transition. The Journal of Clinical Investigation, 119, 1420–1428.PubMed Kalluri, R., & Weinberg, R. A. (2009). The basics of epithelial–mesenchymal transition. The Journal of Clinical Investigation, 119, 1420–1428.PubMed
60.
go back to reference Mani, S. A., Guo, W., Liao, M. J., et al. (2008). The epithelial–mesenchymal transition generates cells with properties of stem cells. Cell, 133, 704–715.PubMed Mani, S. A., Guo, W., Liao, M. J., et al. (2008). The epithelial–mesenchymal transition generates cells with properties of stem cells. Cell, 133, 704–715.PubMed
61.
go back to reference Polyak, K., & Weinberg, R. A. (2009). Transitions between epithelial and mesenchymal states: acquisition of malignant and stem cell traits. Nature Reviews. Cancer, 9, 265–273.PubMed Polyak, K., & Weinberg, R. A. (2009). Transitions between epithelial and mesenchymal states: acquisition of malignant and stem cell traits. Nature Reviews. Cancer, 9, 265–273.PubMed
62.
go back to reference Thompson, E. W., Newgreen, D. F., & Tarin, D. (2005). Carcinoma invasion and metastasis: a role for epithelial–mesenchymal transition? Cancer Research, 65, 5991–5995. discussion 5995.PubMed Thompson, E. W., Newgreen, D. F., & Tarin, D. (2005). Carcinoma invasion and metastasis: a role for epithelial–mesenchymal transition? Cancer Research, 65, 5991–5995. discussion 5995.PubMed
63.
go back to reference Kang, Y., & Massague, J. (2004). Epithelial–mesenchymal transitions: twist in development and metastasis. Cell, 118, 277–279.PubMed Kang, Y., & Massague, J. (2004). Epithelial–mesenchymal transitions: twist in development and metastasis. Cell, 118, 277–279.PubMed
64.
go back to reference Zeng, Q., Li, W., Lu, D., et al. (2012). CD146, an epithelial–mesenchymal transition inducer, is associated with triple-negative breast cancer. Proceedings of the National Academy of Sciences of the United States of America, 109, 1127–1132.PubMed Zeng, Q., Li, W., Lu, D., et al. (2012). CD146, an epithelial–mesenchymal transition inducer, is associated with triple-negative breast cancer. Proceedings of the National Academy of Sciences of the United States of America, 109, 1127–1132.PubMed
65.
go back to reference Trimboli, A. J., Fukino, K., de Bruin, A., et al. (2008). Direct evidence for epithelial–mesenchymal transitions in breast cancer. Cancer Research, 68, 937–945.PubMed Trimboli, A. J., Fukino, K., de Bruin, A., et al. (2008). Direct evidence for epithelial–mesenchymal transitions in breast cancer. Cancer Research, 68, 937–945.PubMed
66.
go back to reference Thiery, J. P., Acloque, H., Huang, R. Y., et al. (2009). Epithelial–mesenchymal transitions in development and disease. Cell, 139, 871–890.PubMed Thiery, J. P., Acloque, H., Huang, R. Y., et al. (2009). Epithelial–mesenchymal transitions in development and disease. Cell, 139, 871–890.PubMed
67.
go back to reference Trelstad, R. L., Hay, E. D., & Revel, J. D. (1967). Cell contact during early morphogenesis in the chick embryo. Developmental Biology, 16, 78–106.PubMed Trelstad, R. L., Hay, E. D., & Revel, J. D. (1967). Cell contact during early morphogenesis in the chick embryo. Developmental Biology, 16, 78–106.PubMed
68.
go back to reference Hay, E. (1968). Organization and fine structure of epithelium and mesenchyme in the developing chick embryo. In R. Fleischmajer & R. Billingham (Eds.), Epithelial mesenchymal interactions. Baltimore: Williams and Wilkins. Hay, E. (1968). Organization and fine structure of epithelium and mesenchyme in the developing chick embryo. In R. Fleischmajer & R. Billingham (Eds.), Epithelial mesenchymal interactions. Baltimore: Williams and Wilkins.
69.
go back to reference Yang, J., & Weinberg, R. A. (2008). Epithelial–mesenchymal transition: at the crossroads of development and tumor metastasis. Developmental Cell, 14, 818–829.PubMed Yang, J., & Weinberg, R. A. (2008). Epithelial–mesenchymal transition: at the crossroads of development and tumor metastasis. Developmental Cell, 14, 818–829.PubMed
70.
go back to reference Tarin, D. (1971). Histological features of neural induction in Xenopus laevis. Journal of Embryology and Experimental Morphology, 26, 543–570.PubMed Tarin, D. (1971). Histological features of neural induction in Xenopus laevis. Journal of Embryology and Experimental Morphology, 26, 543–570.PubMed
71.
go back to reference Tarin, D. (1971). Scanning electron microscopical studies of the embryonic surface during gastrulation and neurulation in Xenopus laevis. Journal of Anatomy, 109, 535–547.PubMed Tarin, D. (1971). Scanning electron microscopical studies of the embryonic surface during gastrulation and neurulation in Xenopus laevis. Journal of Anatomy, 109, 535–547.PubMed
72.
go back to reference Tarin, D. (1972). Ultrastructural features of neural induction in Xenopus laevis. Journal of Anatomy, 111, 1–28.PubMed Tarin, D. (1972). Ultrastructural features of neural induction in Xenopus laevis. Journal of Anatomy, 111, 1–28.PubMed
73.
go back to reference Tarin, D., & Sturdee, A. P. (1971). Early limb development of Xenopus laevis. Journal of Embryology and Experimental Morphology, 26, 169–179.PubMed Tarin, D., & Sturdee, A. P. (1971). Early limb development of Xenopus laevis. Journal of Embryology and Experimental Morphology, 26, 169–179.PubMed
74.
go back to reference Tarin, D., & Sturdee, A. P. (1974). Ultrastructural features of ectodermal–mesenchymal relationships in the developing limb of Xenopus laevis. Journal of Embryology and Experimental Morphology, 31, 287–303.PubMed Tarin, D., & Sturdee, A. P. (1974). Ultrastructural features of ectodermal–mesenchymal relationships in the developing limb of Xenopus laevis. Journal of Embryology and Experimental Morphology, 31, 287–303.PubMed
75.
go back to reference Toivonen, S., Tarin, D., & Saxen, L. (1976). The transmission of morphogenetic signals from amphibian mesoderm to ectoderm in primary induction. Differentiation, 5, 49–55.PubMed Toivonen, S., Tarin, D., & Saxen, L. (1976). The transmission of morphogenetic signals from amphibian mesoderm to ectoderm in primary induction. Differentiation, 5, 49–55.PubMed
76.
go back to reference Tarin, D. (2005). The fallacy of epithelial mesenchymal transition in neoplasia. Cancer Research, 65, 5996–6000.PubMed Tarin, D. (2005). The fallacy of epithelial mesenchymal transition in neoplasia. Cancer Research, 65, 5996–6000.PubMed
77.
go back to reference Gise, A., & Pu, W. T. (2012). Endocardial and epicardial epithelial to mesenchymal transitions in heart development and disease. Circulation Research, 110, 1628–1645. Gise, A., & Pu, W. T. (2012). Endocardial and epicardial epithelial to mesenchymal transitions in heart development and disease. Circulation Research, 110, 1628–1645.
78.
go back to reference Korsching, E., Packeisen, J., Liedtke, C., et al. (2005). The origin of vimentin expression in invasive breast cancer: epithelial–mesenchymal transition, myoepithelial histogenesis or histogenesis from progenitor cells with bilinear differentiation potential? The Journal of Pathology, 206, 451–457.PubMed Korsching, E., Packeisen, J., Liedtke, C., et al. (2005). The origin of vimentin expression in invasive breast cancer: epithelial–mesenchymal transition, myoepithelial histogenesis or histogenesis from progenitor cells with bilinear differentiation potential? The Journal of Pathology, 206, 451–457.PubMed
80.
go back to reference Sucheston, M. E., & Cannon, M. S. (1968). Development of zonular patterns in the human adrenal gland. Journal of Morphology, 126, 477–491.PubMed Sucheston, M. E., & Cannon, M. S. (1968). Development of zonular patterns in the human adrenal gland. Journal of Morphology, 126, 477–491.PubMed
81.
go back to reference Kempna, P., & Fluck, C. E. (2008). Adrenal gland development and defects. Best Practice & Research. Clinical Endocrinology & Metabolism, 22, 77–93. Kempna, P., & Fluck, C. E. (2008). Adrenal gland development and defects. Best Practice & Research. Clinical Endocrinology & Metabolism, 22, 77–93.
82.
go back to reference Satoh, M. (1991). Histogenesis and organogenesis of the gonad in human embryos. Journal of Anatomy, 177, 85–107.PubMed Satoh, M. (1991). Histogenesis and organogenesis of the gonad in human embryos. Journal of Anatomy, 177, 85–107.PubMed
83.
go back to reference Kalluri, R., & Neilson, E. G. (2003). Epithelial–mesenchymal transition and its implications for fibrosis. The Journal of Clinical Investigation, 112, 1776–1784.PubMed Kalluri, R., & Neilson, E. G. (2003). Epithelial–mesenchymal transition and its implications for fibrosis. The Journal of Clinical Investigation, 112, 1776–1784.PubMed
84.
go back to reference Osterreicher, C. H., Penz-Osterreicher, M., Grivennikov, S. I., et al. (2011). Fibroblast-specific protein 1 identifies an inflammatory subpopulation of macrophages in the liver. Proceedings of the National Academy of Sciences of the United States of America, 108, 308–313.PubMed Osterreicher, C. H., Penz-Osterreicher, M., Grivennikov, S. I., et al. (2011). Fibroblast-specific protein 1 identifies an inflammatory subpopulation of macrophages in the liver. Proceedings of the National Academy of Sciences of the United States of America, 108, 308–313.PubMed
85.
go back to reference Humphreys, B. D., Lin, S. L., Kobayashi, A., et al. (2010). Fate tracing reveals the pericyte and not epithelial origin of myofibroblasts in kidney fibrosis. The American Journal of Pathology, 176, 85–97.PubMed Humphreys, B. D., Lin, S. L., Kobayashi, A., et al. (2010). Fate tracing reveals the pericyte and not epithelial origin of myofibroblasts in kidney fibrosis. The American Journal of Pathology, 176, 85–97.PubMed
86.
go back to reference Tomaskovic-Crook, E., Thompson, E. W., & Thiery, J. P. (2009). Epithelial to mesenchymal transition and breast cancer. Breast Cancer Research, 11, 213.PubMed Tomaskovic-Crook, E., Thompson, E. W., & Thiery, J. P. (2009). Epithelial to mesenchymal transition and breast cancer. Breast Cancer Research, 11, 213.PubMed
87.
go back to reference May, C. D., Sphyris, N., Evans, K. W., et al. (2011). Epithelial–mesenchymal transition and cancer stem cells: a dangerously dynamic duo in breast cancer progression. Breast Cancer Research, 13, 202.PubMed May, C. D., Sphyris, N., Evans, K. W., et al. (2011). Epithelial–mesenchymal transition and cancer stem cells: a dangerously dynamic duo in breast cancer progression. Breast Cancer Research, 13, 202.PubMed
88.
go back to reference Yang, J., Mani, S. A., Donaher, J. L., et al. (2004). Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis. Cell, 117, 927–939.PubMed Yang, J., Mani, S. A., Donaher, J. L., et al. (2004). Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis. Cell, 117, 927–939.PubMed
89.
go back to reference Chui, M. H. (2012). Insights into cancer metastasis from a clinicopathologic perspective: epithelial mesenchymal transition is not a necessary step. International Journal of Cancer Journal International du Cancer. doi:10.1002/ijc.27745.PubMed Chui, M. H. (2012). Insights into cancer metastasis from a clinicopathologic perspective: epithelial mesenchymal transition is not a necessary step. International Journal of Cancer Journal International du Cancer. doi:10.​1002/​ijc.​27745.PubMed
90.
go back to reference Cardiff, R. D. (2010). The pathology of EMT in mouse mammary tumorigenesis. Journal of Mammary Gland Biology and Neoplasia, 15, 225–233.PubMed Cardiff, R. D. (2010). The pathology of EMT in mouse mammary tumorigenesis. Journal of Mammary Gland Biology and Neoplasia, 15, 225–233.PubMed
91.
go back to reference Hennessy, B. T., Gonzalez-Angulo, A. M., Stemke-Hale, K., et al. (2009). Characterization of a naturally occurring breast cancer subset enriched in epithelial-to-mesenchymal transition and stem cell characteristics. Cancer Research, 69, 4116–4124.PubMed Hennessy, B. T., Gonzalez-Angulo, A. M., Stemke-Hale, K., et al. (2009). Characterization of a naturally occurring breast cancer subset enriched in epithelial-to-mesenchymal transition and stem cell characteristics. Cancer Research, 69, 4116–4124.PubMed
92.
go back to reference Taube, J. H., Herschkowitz, J. I., Komurov, K., et al. (2010). Core epithelial-to-mesenchymal transition interactome gene-expression signature is associated with claudin-low and metaplastic breast cancer subtypes. Proceedings of the National Academy of Sciences of the United States of America, 107, 15449–15454.PubMed Taube, J. H., Herschkowitz, J. I., Komurov, K., et al. (2010). Core epithelial-to-mesenchymal transition interactome gene-expression signature is associated with claudin-low and metaplastic breast cancer subtypes. Proceedings of the National Academy of Sciences of the United States of America, 107, 15449–15454.PubMed
93.
go back to reference Brabletz, T. (2012). To differentiate or not—routes towards metastasis. Nature Reviews. Cancer, 12, 425–436.PubMed Brabletz, T. (2012). To differentiate or not—routes towards metastasis. Nature Reviews. Cancer, 12, 425–436.PubMed
94.
go back to reference Brabletz, T., Jung, A., Reu, S., et al. (2001). Variable beta-catenin expression in colorectal cancers indicates tumor progression driven by the tumor environment. Proceedings of the National Academy of Sciences of the United States of America, 98, 10356–10361.PubMed Brabletz, T., Jung, A., Reu, S., et al. (2001). Variable beta-catenin expression in colorectal cancers indicates tumor progression driven by the tumor environment. Proceedings of the National Academy of Sciences of the United States of America, 98, 10356–10361.PubMed
95.
go back to reference Kubiak, R., & Szadowska, A. (1997). Invasive lobular carcinoma: correlations between morphological features, vimentin expression, oestrogen receptor status and prognosis. The Breast, 6, 89–96. Kubiak, R., & Szadowska, A. (1997). Invasive lobular carcinoma: correlations between morphological features, vimentin expression, oestrogen receptor status and prognosis. The Breast, 6, 89–96.
96.
go back to reference Armstrong, A. J., Marengo, M. S., Oltean, S., et al. (2011). Circulating tumor cells from patients with advanced prostate and breast cancer display both epithelial and mesenchymal markers. Molecular Cancer Research, 9, 997–1007.PubMed Armstrong, A. J., Marengo, M. S., Oltean, S., et al. (2011). Circulating tumor cells from patients with advanced prostate and breast cancer display both epithelial and mesenchymal markers. Molecular Cancer Research, 9, 997–1007.PubMed
97.
go back to reference Powell, A. A., Talasaz, A. H., Zhang, H., et al. (2012). Single cell profiling of circulating tumor cells: transcriptional heterogeneity and diversity from breast cancer cell lines. PLoS One, 7, e33788.PubMed Powell, A. A., Talasaz, A. H., Zhang, H., et al. (2012). Single cell profiling of circulating tumor cells: transcriptional heterogeneity and diversity from breast cancer cell lines. PLoS One, 7, e33788.PubMed
98.
go back to reference Sun, Y., Campisi, J., Higano, C., et al. (2012).Treatment-induced damage to the tumor microenvironment promotes prostate cancer therapy resistance through WNT16B. Nature Medicine 18, 1359–1368. Sun, Y., Campisi, J., Higano, C., et al. (2012).Treatment-induced damage to the tumor microenvironment promotes prostate cancer therapy resistance through WNT16B. Nature Medicine 18, 1359–1368.
99.
go back to reference O’Mahony, F. C., Faratian, D., Varley, J., et al. (2012). The use of automated quantitative analysis to evaluate epithelial-to-mesenchymal transition associated proteins in clear cell renal cell carcinoma. PLoS One, 7, e31557.PubMed O’Mahony, F. C., Faratian, D., Varley, J., et al. (2012). The use of automated quantitative analysis to evaluate epithelial-to-mesenchymal transition associated proteins in clear cell renal cell carcinoma. PLoS One, 7, e31557.PubMed
100.
go back to reference Leroy, P., & Mostov, K. E. (2007). Slug is required for cell survival during partial epithelial–mesenchymal transition of HGF-induced tubulogenesis. Molecular Biology of the Cell, 18, 1943–1952.PubMed Leroy, P., & Mostov, K. E. (2007). Slug is required for cell survival during partial epithelial–mesenchymal transition of HGF-induced tubulogenesis. Molecular Biology of the Cell, 18, 1943–1952.PubMed
101.
102.
go back to reference Hugo, H., Ackland, M. L., Blick, T., et al. (2007). Epithelial–mesenchymal and mesenchymal–epithelial transitions in carcinoma progression. Journal of Cellular Physiology, 213, 374–383.PubMed Hugo, H., Ackland, M. L., Blick, T., et al. (2007). Epithelial–mesenchymal and mesenchymal–epithelial transitions in carcinoma progression. Journal of Cellular Physiology, 213, 374–383.PubMed
103.
go back to reference Christiansen, J. J., & Rajasekaran, A. K. (2006). Reassessing epithelial to mesenchymal transition as a prerequisite for carcinoma invasion and metastasis. Cancer Research, 66, 8319–8326.PubMed Christiansen, J. J., & Rajasekaran, A. K. (2006). Reassessing epithelial to mesenchymal transition as a prerequisite for carcinoma invasion and metastasis. Cancer Research, 66, 8319–8326.PubMed
104.
go back to reference Zhou, H., Wu, S., Joo, J. Y., et al. (2009). Generation of induced pluripotent stem cells using recombinant proteins. Cell Stem Cell, 4, 381–384.PubMed Zhou, H., Wu, S., Joo, J. Y., et al. (2009). Generation of induced pluripotent stem cells using recombinant proteins. Cell Stem Cell, 4, 381–384.PubMed
105.
go back to reference Wilmut, I., Schnieke, A. E., McWhir, J., et al. (1997). Viable offspring derived from fetal and adult mammalian cells. Nature, 385, 810–813.PubMed Wilmut, I., Schnieke, A. E., McWhir, J., et al. (1997). Viable offspring derived from fetal and adult mammalian cells. Nature, 385, 810–813.PubMed
106.
go back to reference Chaffer, C. L., Thompson, E. W., & Williams, E. D. (2007). Mesenchymal to epithelial transition in development and disease. Cells, Tissues, Organs, 185, 7–19.PubMed Chaffer, C. L., Thompson, E. W., & Williams, E. D. (2007). Mesenchymal to epithelial transition in development and disease. Cells, Tissues, Organs, 185, 7–19.PubMed
107.
go back to reference Tarin, D. (1967). Sequential electron microscopical study of experimental mouse skin carcinogenesis. International Journal of Cancer, 2, 195–211. Tarin, D. (1967). Sequential electron microscopical study of experimental mouse skin carcinogenesis. International Journal of Cancer, 2, 195–211.
108.
go back to reference Tarin, D. (1976). Cellular interactions in neoplasia. In L. Weiss (Ed.), Fundamental aspects of metastasis (pp. 151–187). Amsterdam: North Holland Publishing Co. Tarin, D. (1976). Cellular interactions in neoplasia. In L. Weiss (Ed.), Fundamental aspects of metastasis (pp. 151–187). Amsterdam: North Holland Publishing Co.
109.
go back to reference Sugino, T., Gorham, H., Yoshida, K., et al. (1996). Progressive loss of CD44 gene expression in invasive bladder cancer. The American Journal of Pathology, 149, 873–882.PubMed Sugino, T., Gorham, H., Yoshida, K., et al. (1996). Progressive loss of CD44 gene expression in invasive bladder cancer. The American Journal of Pathology, 149, 873–882.PubMed
110.
go back to reference Viadana, E., Bross, I. D., & Pickren, J. W. (1973). An autopsy study of some routes of dissemination of cancer of the breast. British Journal of Cancer, 27, 336–340.PubMed Viadana, E., Bross, I. D., & Pickren, J. W. (1973). An autopsy study of some routes of dissemination of cancer of the breast. British Journal of Cancer, 27, 336–340.PubMed
111.
go back to reference Noltenius, C., & Noltenius, H. (1985). Dormant tumor cells in liver and brain. An autopsy study on metastasizing tumors. Pathology Research and Practice, 179, 504–511. Noltenius, C., & Noltenius, H. (1985). Dormant tumor cells in liver and brain. An autopsy study on metastasizing tumors. Pathology Research and Practice, 179, 504–511.
112.
go back to reference Suzuki, M., Mose, E., Galloy, C., et al. (2007). Osteopontin gene expression determines spontaneous metastatic performance of orthotopic human breast cancer xenografts. The American Journal of Pathology, 171, 682–692.PubMed Suzuki, M., Mose, E., Galloy, C., et al. (2007). Osteopontin gene expression determines spontaneous metastatic performance of orthotopic human breast cancer xenografts. The American Journal of Pathology, 171, 682–692.PubMed
113.
go back to reference Urquidi, V., Sloan, D., Kawai, K., et al. (2002). Contrasting expression of thrombospondin-1 and osteopontin correlates with absence or presence of metastatic phenotype in an isogenic model of spontaneous human breast cancer metastasis. Clinical Cancer Research, 8, 61–74.PubMed Urquidi, V., Sloan, D., Kawai, K., et al. (2002). Contrasting expression of thrombospondin-1 and osteopontin correlates with absence or presence of metastatic phenotype in an isogenic model of spontaneous human breast cancer metastasis. Clinical Cancer Research, 8, 61–74.PubMed
114.
go back to reference Agrawal, D., Chen, T., Irby, R., et al. (2002). Osteopontin identified as lead marker of colon cancer progression, using pooled sample expression profiling. Journal of the National Cancer Institute, 94, 513–521.PubMed Agrawal, D., Chen, T., Irby, R., et al. (2002). Osteopontin identified as lead marker of colon cancer progression, using pooled sample expression profiling. Journal of the National Cancer Institute, 94, 513–521.PubMed
115.
go back to reference Ang, C., Chambers, A. F., Tuck, A. B., et al. (2005). Plasma osteopontin levels are predictive of disease stage in patients with transitional cell carcinoma of the bladder. BJU International, 96, 803–805.PubMed Ang, C., Chambers, A. F., Tuck, A. B., et al. (2005). Plasma osteopontin levels are predictive of disease stage in patients with transitional cell carcinoma of the bladder. BJU International, 96, 803–805.PubMed
116.
go back to reference Donati, V., Boldrini, L., Dell’Omodarme, M., et al. (2005). Osteopontin expression and prognostic significance in non-small cell lung cancer. Clinical Cancer Research, 11, 6459–6465.PubMed Donati, V., Boldrini, L., Dell’Omodarme, M., et al. (2005). Osteopontin expression and prognostic significance in non-small cell lung cancer. Clinical Cancer Research, 11, 6459–6465.PubMed
117.
go back to reference Jang, T., Savarese, T., Low, H. P., et al. (2006). Osteopontin expression in intratumoral astrocytes marks tumor progression in gliomas induced by prenatal exposure to N-ethyl-N-nitrosourea. The American Journal of Pathology, 168, 1676–1685.PubMed Jang, T., Savarese, T., Low, H. P., et al. (2006). Osteopontin expression in intratumoral astrocytes marks tumor progression in gliomas induced by prenatal exposure to N-ethyl-N-nitrosourea. The American Journal of Pathology, 168, 1676–1685.PubMed
118.
go back to reference Matusan, K., Dordevic, G., Stipic, D., et al. (2006). Osteopontin expression correlates with prognostic variables and survival in clear cell renal cell carcinoma. Journal of Surgical Oncology, 94, 325–331.PubMed Matusan, K., Dordevic, G., Stipic, D., et al. (2006). Osteopontin expression correlates with prognostic variables and survival in clear cell renal cell carcinoma. Journal of Surgical Oncology, 94, 325–331.PubMed
119.
go back to reference Roland, P. Y., Kelly, F. J., Kulwicki, C. Y., et al. (2004). The benefits of a gynecologic oncologist: a pattern of care study for endometrial cancer treatment. Gynecologic Oncology, 93, 125–130.PubMed Roland, P. Y., Kelly, F. J., Kulwicki, C. Y., et al. (2004). The benefits of a gynecologic oncologist: a pattern of care study for endometrial cancer treatment. Gynecologic Oncology, 93, 125–130.PubMed
120.
go back to reference Wai, P. Y., & Kuo, P. C. (2004). The role of osteopontin in tumor metastasis. The Journal of Surgical Research, 121, 228–241.PubMed Wai, P. Y., & Kuo, P. C. (2004). The role of osteopontin in tumor metastasis. The Journal of Surgical Research, 121, 228–241.PubMed
121.
go back to reference Feng, W., McCabe, N. P., Mahabeleshwar, G. H., et al. (2008). The angiogenic response is dictated by beta3 integrin on bone marrow-derived cells. The Journal of Cell Biology, 183, 1145–1157.PubMed Feng, W., McCabe, N. P., Mahabeleshwar, G. H., et al. (2008). The angiogenic response is dictated by beta3 integrin on bone marrow-derived cells. The Journal of Cell Biology, 183, 1145–1157.PubMed
122.
go back to reference Kelly, P. N., Dakic, A., Adams, J. M., et al. (2007). Tumor growth need not be driven by rare cancer stem cells. Science, 317, 337.PubMed Kelly, P. N., Dakic, A., Adams, J. M., et al. (2007). Tumor growth need not be driven by rare cancer stem cells. Science, 317, 337.PubMed
123.
go back to reference Price, J. E., Syms, A. J., Wallace, J. S., et al. (1986). Cellular immortality, clonogenicity, tumorigenicity and the metastatic phenotype. European Journal of Cancer & Clinical Oncology, 22, 349–355. Price, J. E., Syms, A. J., Wallace, J. S., et al. (1986). Cellular immortality, clonogenicity, tumorigenicity and the metastatic phenotype. European Journal of Cancer & Clinical Oncology, 22, 349–355.
124.
go back to reference Visvader, J. E., & Lindeman, G. J. (2008). Cancer stem cells in solid tumours: accumulating evidence and unresolved questions. Nature Reviews. Cancer, 8, 755–768.PubMed Visvader, J. E., & Lindeman, G. J. (2008). Cancer stem cells in solid tumours: accumulating evidence and unresolved questions. Nature Reviews. Cancer, 8, 755–768.PubMed
125.
go back to reference Wang, G. X., Zhan, Y. A., Hu, H. L., et al. (2012). Mesenchymal stem cells modified to express interferon-beta inhibit the growth of prostate cancer in a mouse model. The Journal of International Medical Research, 40, 317–327.PubMed Wang, G. X., Zhan, Y. A., Hu, H. L., et al. (2012). Mesenchymal stem cells modified to express interferon-beta inhibit the growth of prostate cancer in a mouse model. The Journal of International Medical Research, 40, 317–327.PubMed
126.
go back to reference Schrodinger, E. (1944). What is life (p. 194). Cambridge, UK: Cambridge University Press. Schrodinger, E. (1944). What is life (p. 194). Cambridge, UK: Cambridge University Press.
Metadata
Title
Role of the host stroma in cancer and its therapeutic significance
Author
David Tarin
Publication date
01-12-2013
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 3-4/2013
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-013-9438-4

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