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Erschienen in: Cellular Oncology 6/2012

01.12.2012 | Review

Interpretation of interlocking key issues of cancer stem cells in malignant solid tumors

verfasst von: Wei-hui Liu, Nan You, Ning Zhang, Hong-tao Yan, Tao Wang, Zhu Huang, Hong-bao Liu, Li-jun Tang

Erschienen in: Cellular Oncology | Ausgabe 6/2012

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Abstract

Objective

In this review, several interlinking issues related to cancer stem cells (CSCs) in malignant solid tumors are sequentially discussed.

Methods

A literature search was performed using PubMed, Web of Science and the Cochrane library, combining the words CSCs, solid tumor, isolation, identification, origination, therapy, target and epithelial–mesenchymal transition.

Results

Because a primary problem is the isolation of CSCs, we first analyzed the advantages and disadvantages of recently used methods, which were mostly based on the physical or immunochemical characteristics of CSCs. Once CSCs are isolated, they should be identified by their stem cell properties. Here, we suggest how to establish a standard identification strategy. We also focused on the origination hypotheses of CSCs. The supporting molecular mechanisms for each theory were thoroughly analyzed and integrated. Especially, epithelial– mesenchymal transition is an increasingly recognized mechanism to generate CSCs that are endowed with a more invasive and metastatic phenotype. Finally, we discuss putative strategies of eliminating CSCs as effective cancer therapies.

Conclusion

After several interlocking issues of CSCs are thoroughly clarified, these CSCs in solid malignant tumors may specifically be targeted, which raises a new hope for eliminating these tumors.
Literatur
1.
Zurück zum Zitat H. Clevers, The cancer stem cell: premises, promises and challenges. Nat. Med. 17(3), 313–319 (2011)PubMedCrossRef H. Clevers, The cancer stem cell: premises, promises and challenges. Nat. Med. 17(3), 313–319 (2011)PubMedCrossRef
2.
Zurück zum Zitat T. Ikegami, Transforming growth factor-beta signaling and liver cancer stem cell. Hepatol Res. 39(9), 847–849 (2009)PubMedCrossRef T. Ikegami, Transforming growth factor-beta signaling and liver cancer stem cell. Hepatol Res. 39(9), 847–849 (2009)PubMedCrossRef
3.
Zurück zum Zitat M.F. Clarke, J.E. Dick, P.B. Dirks, C.J. Eaves, C.H. Jamieson, D.L. Jones et al., Cancer stem cells–perspectives on current status and future directions: AACR Workshop on cancer stem cells. Cancer Res. 66(19), 9339–9344 (2006)PubMedCrossRef M.F. Clarke, J.E. Dick, P.B. Dirks, C.J. Eaves, C.H. Jamieson, D.L. Jones et al., Cancer stem cells–perspectives on current status and future directions: AACR Workshop on cancer stem cells. Cancer Res. 66(19), 9339–9344 (2006)PubMedCrossRef
4.
Zurück zum Zitat M. Balic, H. Lin, L. Young, D. Hawes, A. Giuliano, G. McNamara et al., Most early disseminated cancer cells detected in bone marrow of breast cancer patients have a putative breast cancer stem cell phenotype. Clin. Cancer Res. 12(19), 5615–5621 (2006)PubMedCrossRef M. Balic, H. Lin, L. Young, D. Hawes, A. Giuliano, G. McNamara et al., Most early disseminated cancer cells detected in bone marrow of breast cancer patients have a putative breast cancer stem cell phenotype. Clin. Cancer Res. 12(19), 5615–5621 (2006)PubMedCrossRef
5.
Zurück zum Zitat G. Gu, J. Yuan, M. Wills, S. Kasper, Prostate cancer cells with stem cell characteristics reconstitute the original human tumor in vivo. Cancer Res. 67(10), 4807–4815 (2007)PubMedCrossRef G. Gu, J. Yuan, M. Wills, S. Kasper, Prostate cancer cells with stem cell characteristics reconstitute the original human tumor in vivo. Cancer Res. 67(10), 4807–4815 (2007)PubMedCrossRef
6.
Zurück zum Zitat S. Takaishi, T. Okumura, S. Tu, S.S. Wang, W. Shibata, R. Vigneshwaran et al., Identification of gastric cancer stem cells using the cell surface marker CD44. Stem Cells 27(5), 1006–1020 (2009)PubMedCrossRef S. Takaishi, T. Okumura, S. Tu, S.S. Wang, W. Shibata, R. Vigneshwaran et al., Identification of gastric cancer stem cells using the cell surface marker CD44. Stem Cells 27(5), 1006–1020 (2009)PubMedCrossRef
7.
Zurück zum Zitat M. Todaro, M.G. Francipane, J.P. Medema, G. Stassi, Colon cancer stem cells: Promise of targeted therapy. Gastroenterology 138(6), 2151–2162 (2010)PubMedCrossRef M. Todaro, M.G. Francipane, J.P. Medema, G. Stassi, Colon cancer stem cells: Promise of targeted therapy. Gastroenterology 138(6), 2151–2162 (2010)PubMedCrossRef
8.
Zurück zum Zitat T. Chiba, A. Kamiya, O. Yokosuka, A. Iwama, Cancer stem cells in hepatocellular carcinoma: Recent progress and perspective. Cancer Lett. 286(2), 145–153 (2009)PubMedCrossRef T. Chiba, A. Kamiya, O. Yokosuka, A. Iwama, Cancer stem cells in hepatocellular carcinoma: Recent progress and perspective. Cancer Lett. 286(2), 145–153 (2009)PubMedCrossRef
9.
Zurück zum Zitat T. Shupe, B.E. Petersen, Evidence regarding a stem cell origin of hepatocellular carcinoma. Stem Cell Rev. 1(3), 261–264 (2005)PubMedCrossRef T. Shupe, B.E. Petersen, Evidence regarding a stem cell origin of hepatocellular carcinoma. Stem Cell Rev. 1(3), 261–264 (2005)PubMedCrossRef
10.
Zurück zum Zitat M. Baddoo, K. Hill, R. Wilkinson, D. Gaupp, C. Hughes, G.C. Kopen et al., Characterization of mesenchymal stem cells isolated from murine bone marrow by negative selection. J. Cell. Biochem. 89(6), 1235–1249 (2003)PubMedCrossRef M. Baddoo, K. Hill, R. Wilkinson, D. Gaupp, C. Hughes, G.C. Kopen et al., Characterization of mesenchymal stem cells isolated from murine bone marrow by negative selection. J. Cell. Biochem. 89(6), 1235–1249 (2003)PubMedCrossRef
11.
Zurück zum Zitat F.I. Ghani, H. Yamazaki, S. Iwata, T. Okamoto, K. Aoe, K. Okabe et al., Identification of cancer stem cell markers in human malignant mesothelioma cells. Biochem. Biophys. Res. Commun. 404(2), 735–742 (2011)PubMedCrossRef F.I. Ghani, H. Yamazaki, S. Iwata, T. Okamoto, K. Aoe, K. Okabe et al., Identification of cancer stem cell markers in human malignant mesothelioma cells. Biochem. Biophys. Res. Commun. 404(2), 735–742 (2011)PubMedCrossRef
12.
Zurück zum Zitat S. Shigdar, J. Lin, Y. Yu, M. Pastuovic, M. Wei, W. Duan, RNA aptamer against a cancer stem cell marker epithelial cell adhesion molecule. Cancer Sci. 102(5), 991–998 (2011)PubMedCrossRef S. Shigdar, J. Lin, Y. Yu, M. Pastuovic, M. Wei, W. Duan, RNA aptamer against a cancer stem cell marker epithelial cell adhesion molecule. Cancer Sci. 102(5), 991–998 (2011)PubMedCrossRef
13.
Zurück zum Zitat K. Kohga, T. Tatsumi, T. Takehara, H. Tsunematsu, S. Shimizu, M. Yamamoto et al., Expression of CD133 confers malignant potential by regulating metalloproteinases in human hepatocellular carcinoma. J. Hepatol. 52(6), 872–879 (2010)PubMedCrossRef K. Kohga, T. Tatsumi, T. Takehara, H. Tsunematsu, S. Shimizu, M. Yamamoto et al., Expression of CD133 confers malignant potential by regulating metalloproteinases in human hepatocellular carcinoma. J. Hepatol. 52(6), 872–879 (2010)PubMedCrossRef
14.
Zurück zum Zitat L. Vermeulen, M. Todaro, F. de Sousa Mello, M.R. Sprick, K. Kemper, M. Perez Alea et al., Single-cell cloning of colon cancer stem cells reveals a multi-lineage differentiation capacity. Proc. Natl. Acad. Sci. U. S. A. 105(36), 13427–13432 (2008)PubMedCrossRef L. Vermeulen, M. Todaro, F. de Sousa Mello, M.R. Sprick, K. Kemper, M. Perez Alea et al., Single-cell cloning of colon cancer stem cells reveals a multi-lineage differentiation capacity. Proc. Natl. Acad. Sci. U. S. A. 105(36), 13427–13432 (2008)PubMedCrossRef
15.
Zurück zum Zitat L.S. Hart, N.G. Dolloff, D.T. Dicker, C. Koumenis, J.G. Christensen, A. Grimberg et al., Human colon cancer stem cells are enriched by insulin-like growth factor-1 and are sensitive to figitumumab. Cell Cycle 10(14), 2331–2338 (2011)PubMedCrossRef L.S. Hart, N.G. Dolloff, D.T. Dicker, C. Koumenis, J.G. Christensen, A. Grimberg et al., Human colon cancer stem cells are enriched by insulin-like growth factor-1 and are sensitive to figitumumab. Cell Cycle 10(14), 2331–2338 (2011)PubMedCrossRef
16.
Zurück zum Zitat F.J. Abdul Khalek, G.I. Gallicano, L. Mishra, Colon cancer stem cells. Gastrointest Cancer Res 1, S16–S23 (2010) F.J. Abdul Khalek, G.I. Gallicano, L. Mishra, Colon cancer stem cells. Gastrointest Cancer Res 1, S16–S23 (2010)
17.
Zurück zum Zitat W. Song, H. Li, K. Tao, R. Li, Z. Song, Q. Zhao et al., Expression and clinical significance of the stem cell marker CD133 in hepatocellular carcinoma. Int. J. Clin. Pract. 62(8), 1212–1218 (2008)PubMedCrossRef W. Song, H. Li, K. Tao, R. Li, Z. Song, Q. Zhao et al., Expression and clinical significance of the stem cell marker CD133 in hepatocellular carcinoma. Int. J. Clin. Pract. 62(8), 1212–1218 (2008)PubMedCrossRef
18.
Zurück zum Zitat T. Nagata, C. Sakakura, S. Komiyama, A. Miyashita, M. Nishio, Y. Murayama et al., Expression of cancer stem cell markers CD133 and CD44 in locoregional recurrence of rectal cancer. Anticancer Res. 31(2), 495–500 (2011)PubMed T. Nagata, C. Sakakura, S. Komiyama, A. Miyashita, M. Nishio, Y. Murayama et al., Expression of cancer stem cell markers CD133 and CD44 in locoregional recurrence of rectal cancer. Anticancer Res. 31(2), 495–500 (2011)PubMed
19.
Zurück zum Zitat T. Yamashita, J. Ji, A. Budhu, M. Forgues, W. Yang, H.Y. Wang et al., EpCAM-positive hepatocellular carcinoma cells are tumor-initiating cells with stem/progenitor cell features. Gastroenterology 136(3), 1012–1024 (2009)PubMedCrossRef T. Yamashita, J. Ji, A. Budhu, M. Forgues, W. Yang, H.Y. Wang et al., EpCAM-positive hepatocellular carcinoma cells are tumor-initiating cells with stem/progenitor cell features. Gastroenterology 136(3), 1012–1024 (2009)PubMedCrossRef
20.
Zurück zum Zitat Z.F. Yang, P. Ngai, D.W. Ho, W.C. Yu, M.N. Ng, C.K. Lau et al., Identification of local and circulating cancer stem cells in human liver cancer. Hepatology 47(3), 919–928 (2008)PubMedCrossRef Z.F. Yang, P. Ngai, D.W. Ho, W.C. Yu, M.N. Ng, C.K. Lau et al., Identification of local and circulating cancer stem cells in human liver cancer. Hepatology 47(3), 919–928 (2008)PubMedCrossRef
21.
Zurück zum Zitat H. Yanai, K. Nakamura, S. Hijioka, A. Kamei, T. Ikari, Y. Ishikawa et al., Dlk-1, a cell surface antigen on foetal hepatic stem/progenitor cells, is expressed in hepatocellular, colon, pancreas and breast carcinomas at a high frequency. J. Biochem. 148(1), 85–92 (2010)PubMedCrossRef H. Yanai, K. Nakamura, S. Hijioka, A. Kamei, T. Ikari, Y. Ishikawa et al., Dlk-1, a cell surface antigen on foetal hepatic stem/progenitor cells, is expressed in hepatocellular, colon, pancreas and breast carcinomas at a high frequency. J. Biochem. 148(1), 85–92 (2010)PubMedCrossRef
22.
Zurück zum Zitat B. Christ, P. Stock, M.M. Dollinger, CD13: Waving the flag for a novel cancer stem cell target. Hepatology 53(4), 1388–1390 (2011)PubMedCrossRef B. Christ, P. Stock, M.M. Dollinger, CD13: Waving the flag for a novel cancer stem cell target. Hepatology 53(4), 1388–1390 (2011)PubMedCrossRef
23.
Zurück zum Zitat W. Yang, H.X. Yan, L. Chen, Q. Liu, Y.Q. He, L.X. Yu et al., Wnt/beta-catenin signaling contributes to activation of normal and tumorigenic liver progenitor cells. Cancer Res. 68(11), 4287–4295 (2008)PubMedCrossRef W. Yang, H.X. Yan, L. Chen, Q. Liu, Y.Q. He, L.X. Yu et al., Wnt/beta-catenin signaling contributes to activation of normal and tumorigenic liver progenitor cells. Cancer Res. 68(11), 4287–4295 (2008)PubMedCrossRef
24.
Zurück zum Zitat S. Lingala, Y.Y. Cui, X. Chen, B.H. Ruebner, X.F. Qian, M.A. Zern et al., Immunohistochemical staining of cancer stem cell markers in hepatocellular carcinoma. Exp. Mol. Pathol. 89(1), 27–35 (2010)PubMedCrossRef S. Lingala, Y.Y. Cui, X. Chen, B.H. Ruebner, X.F. Qian, M.A. Zern et al., Immunohistochemical staining of cancer stem cell markers in hepatocellular carcinoma. Exp. Mol. Pathol. 89(1), 27–35 (2010)PubMedCrossRef
25.
Zurück zum Zitat Z. Zhu, X. Hao, M. Yan, M. Yao, C. Ge, J. Gu et al., Cancer stem/progenitor cells are highly enriched in CD133 + CD44+ population in hepatocellular carcinoma. Int. J. Cancer 126(9), 2067–2078 (2010)PubMed Z. Zhu, X. Hao, M. Yan, M. Yao, C. Ge, J. Gu et al., Cancer stem/progenitor cells are highly enriched in CD133 + CD44+ population in hepatocellular carcinoma. Int. J. Cancer 126(9), 2067–2078 (2010)PubMed
26.
Zurück zum Zitat X.R. Yang, Y. Xu, B. Yu, J. Zhou, S.J. Qiu, G.M. Shi et al., High expression levels of putative hepatic stem/progenitor cell biomarkers related to tumour angiogenesis and poor prognosis of hepatocellular carcinoma. Gut 59(7), 953–962 (2010)PubMedCrossRef X.R. Yang, Y. Xu, B. Yu, J. Zhou, S.J. Qiu, G.M. Shi et al., High expression levels of putative hepatic stem/progenitor cell biomarkers related to tumour angiogenesis and poor prognosis of hepatocellular carcinoma. Gut 59(7), 953–962 (2010)PubMedCrossRef
27.
Zurück zum Zitat T. Fujii, Y. Zen, K. Harada, H. Niwa, S. Masuda, Y. Kaizaki et al., Participation of liver cancer stem/progenitor cells in tumorigenesis of scirrhous hepatocellular carcinoma–human and cell culture study. Hum. Pathol. 39(8), 1185–1196 (2008)PubMedCrossRef T. Fujii, Y. Zen, K. Harada, H. Niwa, S. Masuda, Y. Kaizaki et al., Participation of liver cancer stem/progenitor cells in tumorigenesis of scirrhous hepatocellular carcinoma–human and cell culture study. Hum. Pathol. 39(8), 1185–1196 (2008)PubMedCrossRef
28.
Zurück zum Zitat M.A. Goodell, K. Brose, G. Paradis, A.S. Conner, R.C. Mulligan, Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo. J. Exp. Med. 183(4), 1797–1806 (1996)PubMedCrossRef M.A. Goodell, K. Brose, G. Paradis, A.S. Conner, R.C. Mulligan, Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo. J. Exp. Med. 183(4), 1797–1806 (1996)PubMedCrossRef
29.
Zurück zum Zitat G.J. Spangrude, G.R. Johnson, Resting and activated subsets of mouse multipotent hematopoietic stem cells. Proc Natl Acad Sci USA 87(19), 7433–7437 (1990)PubMedCrossRef G.J. Spangrude, G.R. Johnson, Resting and activated subsets of mouse multipotent hematopoietic stem cells. Proc Natl Acad Sci USA 87(19), 7433–7437 (1990)PubMedCrossRef
30.
Zurück zum Zitat A. Asakura, P. Seale, A. Girgis-Gabardo, M.A. Rudnicki, Myogenic specification of side population cells in skeletal muscle. J. Cell Biol. 159(1), 123–134 (2002)PubMedCrossRef A. Asakura, P. Seale, A. Girgis-Gabardo, M.A. Rudnicki, Myogenic specification of side population cells in skeletal muscle. J. Cell Biol. 159(1), 123–134 (2002)PubMedCrossRef
31.
Zurück zum Zitat A.J. Alvi, H. Clayton, C. Joshi, T. Enver, A. Ashworth, M.M. Vivanco et al., Functional and molecular characterisation of mammary side population cells. Breast Cancer Res. 5(1), R1–R8 (2003)PubMedCrossRef A.J. Alvi, H. Clayton, C. Joshi, T. Enver, A. Ashworth, M.M. Vivanco et al., Functional and molecular characterisation of mammary side population cells. Breast Cancer Res. 5(1), R1–R8 (2003)PubMedCrossRef
32.
Zurück zum Zitat K. Shimano, M. Satake, A. Okaya, J. Kitanaka, N. Kitanaka, M. Takemura et al., Hepatic oval cells have the side population phenotype defined by expression of ATP-binding cassette transporter ABCG2/BCRP1. Am. J. Pathol. 163(1), 3–9 (2003)PubMedCrossRef K. Shimano, M. Satake, A. Okaya, J. Kitanaka, N. Kitanaka, M. Takemura et al., Hepatic oval cells have the side population phenotype defined by expression of ATP-binding cassette transporter ABCG2/BCRP1. Am. J. Pathol. 163(1), 3–9 (2003)PubMedCrossRef
33.
Zurück zum Zitat C.M. Dekaney, J.M. Rodriguez, M.C. Graul, S.J. Henning, Isolation and characterization of a putative intestinal stem cell fraction from mouse jejunum. Gastroenterology 129(5), 1567–1580 (2005)PubMedCrossRef C.M. Dekaney, J.M. Rodriguez, M.C. Graul, S.J. Henning, Isolation and characterization of a putative intestinal stem cell fraction from mouse jejunum. Gastroenterology 129(5), 1567–1580 (2005)PubMedCrossRef
34.
Zurück zum Zitat M. Ono, T. Maruyama, H. Masuda, T. Kajitani, T. Nagashima, T. Arase et al., Side population in human uterine myometrium displays phenotypic and functional characteristics of myometrial stem cells. Proc. Natl. Acad. Sci. U.S.A. 104(47), 18700–18705 (2007)PubMedCrossRef M. Ono, T. Maruyama, H. Masuda, T. Kajitani, T. Nagashima, T. Arase et al., Side population in human uterine myometrium displays phenotypic and functional characteristics of myometrial stem cells. Proc. Natl. Acad. Sci. U.S.A. 104(47), 18700–18705 (2007)PubMedCrossRef
35.
Zurück zum Zitat T. Chiba, K. Kita, Y.W. Zheng, O. Yokosuka, H. Saisho, A. Iwama et al., Side population purified from hepatocellular carcinoma cells harbors cancer stem cell-like properties. Hepatology 44(1), 240–251 (2006)PubMedCrossRef T. Chiba, K. Kita, Y.W. Zheng, O. Yokosuka, H. Saisho, A. Iwama et al., Side population purified from hepatocellular carcinoma cells harbors cancer stem cell-like properties. Hepatology 44(1), 240–251 (2006)PubMedCrossRef
36.
Zurück zum Zitat G.M. Shi, Y. Xu, J. Fan, J. Zhou, X.R. Yang, S.J. Qiu et al., Identification of side population cells in human hepatocellular carcinoma cell lines with stepwise metastatic potentials. J. Cancer Res. Clin. Oncol. 134(11), 1155–1163 (2008)PubMedCrossRef G.M. Shi, Y. Xu, J. Fan, J. Zhou, X.R. Yang, S.J. Qiu et al., Identification of side population cells in human hepatocellular carcinoma cell lines with stepwise metastatic potentials. J. Cancer Res. Clin. Oncol. 134(11), 1155–1163 (2008)PubMedCrossRef
37.
Zurück zum Zitat Y. Zhang, W.J. Song, F.Q. Zhang, W.H. Liu, K.F. Dou, Differentiation-inducing activity of hydroxycamptothecin on cancer stem-like cells derived from hepatocellular carcinoma. Dig. Dis. Sci. 56(8), 2473–2481 (2011)PubMedCrossRef Y. Zhang, W.J. Song, F.Q. Zhang, W.H. Liu, K.F. Dou, Differentiation-inducing activity of hydroxycamptothecin on cancer stem-like cells derived from hepatocellular carcinoma. Dig. Dis. Sci. 56(8), 2473–2481 (2011)PubMedCrossRef
38.
Zurück zum Zitat W.H. Liu, N.S. Qian, R. Li, K.F. Dou, Replacing Hoechst33342 with rhodamine123 in isolation of cancer stem-like cells from the MHCC97 cell line. Toxicol. In Vitro 24(2), 538–545 (2010)PubMedCrossRef W.H. Liu, N.S. Qian, R. Li, K.F. Dou, Replacing Hoechst33342 with rhodamine123 in isolation of cancer stem-like cells from the MHCC97 cell line. Toxicol. In Vitro 24(2), 538–545 (2010)PubMedCrossRef
39.
Zurück zum Zitat W.H. Liu, K.S. Tao, N. You, Z.C. Liu, H.T. Zhang, K.F. Dou, Differences in the Properties and Mirna Expression Profiles between Side Populations from Hepatic Cancer Cells and Normal Liver Cells. PLoS One 6(8), e23311 (2011)PubMedCrossRef W.H. Liu, K.S. Tao, N. You, Z.C. Liu, H.T. Zhang, K.F. Dou, Differences in the Properties and Mirna Expression Profiles between Side Populations from Hepatic Cancer Cells and Normal Liver Cells. PLoS One 6(8), e23311 (2011)PubMedCrossRef
40.
Zurück zum Zitat Z. Song, R. Li, N. You, K. Tao, K. Dou, Loss of heterozygosity of the tumor suppressor gene Tg737 in the side population cells of hepatocellular carcinomas is associated with poor prognosis. Mol. Biol. Rep. 37(8), 4091–4101 (2010)PubMedCrossRef Z. Song, R. Li, N. You, K. Tao, K. Dou, Loss of heterozygosity of the tumor suppressor gene Tg737 in the side population cells of hepatocellular carcinomas is associated with poor prognosis. Mol. Biol. Rep. 37(8), 4091–4101 (2010)PubMedCrossRef
41.
Zurück zum Zitat A. Golebiewska, N.H. Brons, R. Bjerkvig, S.P. Niclou, Critical appraisal of the side population assay in stem cell and cancer stem cell research. Cell Stem Cell 8(2), 136–147 (2011)PubMedCrossRef A. Golebiewska, N.H. Brons, R. Bjerkvig, S.P. Niclou, Critical appraisal of the side population assay in stem cell and cancer stem cell research. Cell Stem Cell 8(2), 136–147 (2011)PubMedCrossRef
42.
Zurück zum Zitat F. Montanaro, K. Liadaki, J. Schienda, A. Flint, E. Gussoni, L.M. Kunkel, Demystifying SP cell purification: Viability, yield, and phenotype are defined by isolation parameters. Exp. Cell Res. 298(1), 144–154 (2004)PubMedCrossRef F. Montanaro, K. Liadaki, J. Schienda, A. Flint, E. Gussoni, L.M. Kunkel, Demystifying SP cell purification: Viability, yield, and phenotype are defined by isolation parameters. Exp. Cell Res. 298(1), 144–154 (2004)PubMedCrossRef
43.
Zurück zum Zitat C. Ferlini, G. Scambia, Assay for apoptosis using the mitochondrial probes, Rhodamine123 and 10-N-nonyl acridine orange. Nat. Protoc. 2(12), 3111–3114 (2007)PubMedCrossRef C. Ferlini, G. Scambia, Assay for apoptosis using the mitochondrial probes, Rhodamine123 and 10-N-nonyl acridine orange. Nat. Protoc. 2(12), 3111–3114 (2007)PubMedCrossRef
44.
Zurück zum Zitat A.C. Ribou, J. Vigo, E. Kohen, J.M. Salmon, Microfluorometric study of oxygen dependence of (1″-pyrene butyl)-2-rhodamine ester probe in mitochondria of living cells. J. Photochem. Photobiol. B 70(2), 107–115 (2003)PubMedCrossRef A.C. Ribou, J. Vigo, E. Kohen, J.M. Salmon, Microfluorometric study of oxygen dependence of (1″-pyrene butyl)-2-rhodamine ester probe in mitochondria of living cells. J. Photochem. Photobiol. B 70(2), 107–115 (2003)PubMedCrossRef
45.
46.
Zurück zum Zitat A.M. Rosca, A. Burlacu, Isolation of a mouse bone marrow population enriched in stem and progenitor cells by centrifugation on a Percoll gradient. Biotechnol. Appl. Biochem. 55(4), 199–208 (2010)PubMedCrossRef A.M. Rosca, A. Burlacu, Isolation of a mouse bone marrow population enriched in stem and progenitor cells by centrifugation on a Percoll gradient. Biotechnol. Appl. Biochem. 55(4), 199–208 (2010)PubMedCrossRef
47.
Zurück zum Zitat Y. Chang, P.H. Hsieh, C.C. Chao, The efficiency of Percoll and Ficoll density gradient media in the isolation of marrow derived human mesenchymal stem cells with osteogenic potential. Chang Gung Med. J. 32(3), 264–275 (2009)PubMed Y. Chang, P.H. Hsieh, C.C. Chao, The efficiency of Percoll and Ficoll density gradient media in the isolation of marrow derived human mesenchymal stem cells with osteogenic potential. Chang Gung Med. J. 32(3), 264–275 (2009)PubMed
48.
Zurück zum Zitat W.H. Liu, R. Li, K.F. Dou, Convenient and efficient enrichment of the CD133+ liver cells from rat fetal liver cells as a source of liver stem/progenitor cells. Stem Cell Rev. 7(1), 94–102 (2011)PubMedCrossRef W.H. Liu, R. Li, K.F. Dou, Convenient and efficient enrichment of the CD133+ liver cells from rat fetal liver cells as a source of liver stem/progenitor cells. Stem Cell Rev. 7(1), 94–102 (2011)PubMedCrossRef
49.
Zurück zum Zitat W.H. Liu, X. Wang, N. You, K.S. Tao, T. Wang, L.J. Tang et al., Efficient Enrichment of Hepatic Cancer Stem-Like Cells from a Primary Rat HCC Model via a Density Gradient Centrifugation-Centered Method. PLoS One 7(4), e35720 (2012)PubMedCrossRef W.H. Liu, X. Wang, N. You, K.S. Tao, T. Wang, L.J. Tang et al., Efficient Enrichment of Hepatic Cancer Stem-Like Cells from a Primary Rat HCC Model via a Density Gradient Centrifugation-Centered Method. PLoS One 7(4), e35720 (2012)PubMedCrossRef
50.
Zurück zum Zitat N.A. Lobo, Y. Shimono, D. Qian, M.F. Clarke, The biology of cancer stem cells. Annu. Rev. Cell Dev. Biol. 23, 675–699 (2007)PubMedCrossRef N.A. Lobo, Y. Shimono, D. Qian, M.F. Clarke, The biology of cancer stem cells. Annu. Rev. Cell Dev. Biol. 23, 675–699 (2007)PubMedCrossRef
51.
Zurück zum Zitat M.F. Clarke, M. Fuller, Stem cells and cancer: Two faces of eve. Cell 124(6), 1111–1115 (2006)PubMedCrossRef M.F. Clarke, M. Fuller, Stem cells and cancer: Two faces of eve. Cell 124(6), 1111–1115 (2006)PubMedCrossRef
52.
Zurück zum Zitat X. Lu, Y. Kang, Cell fusion hypothesis of the cancer stem cell. Adv. Exp. Med. Biol. 714, 129–140 (2011)PubMedCrossRef X. Lu, Y. Kang, Cell fusion hypothesis of the cancer stem cell. Adv. Exp. Med. Biol. 714, 129–140 (2011)PubMedCrossRef
53.
Zurück zum Zitat T. Yamashita, M. Honda, K. Nio, Y. Nakamoto, H. Takamura, T. Tani et al., Oncostatin m renders epithelial cell adhesion molecule-positive liver cancer stem cells sensitive to 5-Fluorouracil by inducing hepatocytic differentiation. Cancer Res. 70(11), 4687–4697 (2010)PubMedCrossRef T. Yamashita, M. Honda, K. Nio, Y. Nakamoto, H. Takamura, T. Tani et al., Oncostatin m renders epithelial cell adhesion molecule-positive liver cancer stem cells sensitive to 5-Fluorouracil by inducing hepatocytic differentiation. Cancer Res. 70(11), 4687–4697 (2010)PubMedCrossRef
54.
Zurück zum Zitat R. Taghizadeh, M. Noh, Y.H. Huh, E. Ciusani, L. Sigalotti, M. Maio et al., CXCR6, a newly defined biomarker of tissue-specific stem cell asymmetric self-renewal, identifies more aggressive human melanoma cancer stem cells. PLoS One 5(12), e15183 (2010)PubMedCrossRef R. Taghizadeh, M. Noh, Y.H. Huh, E. Ciusani, L. Sigalotti, M. Maio et al., CXCR6, a newly defined biomarker of tissue-specific stem cell asymmetric self-renewal, identifies more aggressive human melanoma cancer stem cells. PLoS One 5(12), e15183 (2010)PubMedCrossRef
55.
Zurück zum Zitat A.G. Schepers, H.J. Snippert, D.E. Stange, M. van den Born, J.H. van Es, M. van de Wetering et al., Lineage tracing reveals Lgr5+ stem cell activity in mouse intestinal adenomas. Science 337(6095), 730–735 (2012)PubMedCrossRef A.G. Schepers, H.J. Snippert, D.E. Stange, M. van den Born, J.H. van Es, M. van de Wetering et al., Lineage tracing reveals Lgr5+ stem cell activity in mouse intestinal adenomas. Science 337(6095), 730–735 (2012)PubMedCrossRef
56.
Zurück zum Zitat A.L. Welm, S. Kim, B.E. Welm, J.M. Bishop, MET and MYC cooperate in mammary tumorigenesis. Proc. Natl. Acad. Sci. U.S.A. 102(12), 4324–4329 (2005)PubMedCrossRef A.L. Welm, S. Kim, B.E. Welm, J.M. Bishop, MET and MYC cooperate in mammary tumorigenesis. Proc. Natl. Acad. Sci. U.S.A. 102(12), 4324–4329 (2005)PubMedCrossRef
57.
Zurück zum Zitat B. Mayer, J.P. Johnson, F. Leitl, K.W. Jauch, M.M. Heiss, F.W. Schildberg et al., E-cadherin expression in primary and metastatic gastric cancer: down-regulation correlates with cellular dedifferentiation and glandular disintegration. Cancer Res. 53(7), 1690–1695 (1993)PubMed B. Mayer, J.P. Johnson, F. Leitl, K.W. Jauch, M.M. Heiss, F.W. Schildberg et al., E-cadherin expression in primary and metastatic gastric cancer: down-regulation correlates with cellular dedifferentiation and glandular disintegration. Cancer Res. 53(7), 1690–1695 (1993)PubMed
58.
Zurück zum Zitat S. Sell, Cellular origin of cancer: Dedifferentiation or stem cell maturation arrest? Environ. Health Perspect. 101(Suppl 5), 15–26 (1993)PubMedCrossRef S. Sell, Cellular origin of cancer: Dedifferentiation or stem cell maturation arrest? Environ. Health Perspect. 101(Suppl 5), 15–26 (1993)PubMedCrossRef
59.
Zurück zum Zitat R. Fossmark, C.M. Zhao, T.C. Martinsen, S. Kawase, D. Chen, H.L. Waldum, Dedifferentiation of enterochromaffin-like cells in gastric cancer of hypergastrinemic cotton rats. APMIS. 113(6), 436–449 (2005)PubMedCrossRef R. Fossmark, C.M. Zhao, T.C. Martinsen, S. Kawase, D. Chen, H.L. Waldum, Dedifferentiation of enterochromaffin-like cells in gastric cancer of hypergastrinemic cotton rats. APMIS. 113(6), 436–449 (2005)PubMedCrossRef
60.
Zurück zum Zitat A.V. Ougolkov, M.E. Fernandez-Zapico, V.N. Bilim, T.C. Smyrk, S.T. Chari, D.D. Billadeau, Aberrant nuclear accumulation of glycogen synthase kinase-3beta in human pancreatic cancer: association with kinase activity and tumor dedifferentiation. Clin. Cancer Res. 12(17), 5074–5081 (2006)PubMedCrossRef A.V. Ougolkov, M.E. Fernandez-Zapico, V.N. Bilim, T.C. Smyrk, S.T. Chari, D.D. Billadeau, Aberrant nuclear accumulation of glycogen synthase kinase-3beta in human pancreatic cancer: association with kinase activity and tumor dedifferentiation. Clin. Cancer Res. 12(17), 5074–5081 (2006)PubMedCrossRef
61.
Zurück zum Zitat Y. Oku, T. Shimoji, K. Takifuji, T. Hotta, S. Yokoyama, K. Matsuda et al., Identification of the molecular mechanisms for dedifferentiation at the invasion front of colorectal cancer by a gene expression analysis. Clin. Cancer Res. 14(22), 7215–7222 (2008)PubMedCrossRef Y. Oku, T. Shimoji, K. Takifuji, T. Hotta, S. Yokoyama, K. Matsuda et al., Identification of the molecular mechanisms for dedifferentiation at the invasion front of colorectal cancer by a gene expression analysis. Clin. Cancer Res. 14(22), 7215–7222 (2008)PubMedCrossRef
62.
Zurück zum Zitat R.J. Gilbertson, T.A. Graham, Cancer: Resolving the stem-cell debate. Nature 488(7412), 462–463 (2012)PubMedCrossRef R.J. Gilbertson, T.A. Graham, Cancer: Resolving the stem-cell debate. Nature 488(7412), 462–463 (2012)PubMedCrossRef
63.
Zurück zum Zitat J. Chen, Y. Li, T.S. Yu, R.M. McKay, D.K. Burns, S.G. Kernie et al., A restricted cell population propagates glioblastoma growth after chemotherapy. Nature 488(7412), 522–526 (2012)PubMedCrossRef J. Chen, Y. Li, T.S. Yu, R.M. McKay, D.K. Burns, S.G. Kernie et al., A restricted cell population propagates glioblastoma growth after chemotherapy. Nature 488(7412), 522–526 (2012)PubMedCrossRef
64.
Zurück zum Zitat G. Driessens, B. Beck, A. Caauwe, B.D. Simons, C. Blanpain, Defining the mode of tumour growth by clonal analysis. Nature 488(7412), 527–530 (2012)PubMedCrossRef G. Driessens, B. Beck, A. Caauwe, B.D. Simons, C. Blanpain, Defining the mode of tumour growth by clonal analysis. Nature 488(7412), 527–530 (2012)PubMedCrossRef
65.
Zurück zum Zitat A.V. Salnikov, G. Kusumawidjaja, V. Rausch, H. Bruns, W. Gross, A. Khamidjanov et al., Cancer stem cell marker expression in hepatocellular carcinoma and liver metastases is not sufficient as single prognostic parameter. Cancer Lett. 275(2), 185–193 (2009)PubMedCrossRef A.V. Salnikov, G. Kusumawidjaja, V. Rausch, H. Bruns, W. Gross, A. Khamidjanov et al., Cancer stem cell marker expression in hepatocellular carcinoma and liver metastases is not sufficient as single prognostic parameter. Cancer Lett. 275(2), 185–193 (2009)PubMedCrossRef
66.
Zurück zum Zitat T. Chiba, S. Miyagi, A. Saraya, R. Aoki, A. Seki, Y. Morita et al., The polycomb gene product BMI1 contributes to the maintenance of tumor-initiating side population cells in hepatocellular carcinoma. Cancer Res. 68(19), 7742–7749 (2008)PubMedCrossRef T. Chiba, S. Miyagi, A. Saraya, R. Aoki, A. Seki, Y. Morita et al., The polycomb gene product BMI1 contributes to the maintenance of tumor-initiating side population cells in hepatocellular carcinoma. Cancer Res. 68(19), 7742–7749 (2008)PubMedCrossRef
67.
Zurück zum Zitat J.P. Li, J.Y. Zheng, J.J. Du, R. Zhang, A.G. Yang, What is the relationship among microRNA-181, epithelial cell-adhesion molecule (EpCAM) and beta-catenin in hepatic cancer stem cells. Hepatology 50(6), 2047–2048 (2009). author reply 448PubMedCrossRef J.P. Li, J.Y. Zheng, J.J. Du, R. Zhang, A.G. Yang, What is the relationship among microRNA-181, epithelial cell-adhesion molecule (EpCAM) and beta-catenin in hepatic cancer stem cells. Hepatology 50(6), 2047–2048 (2009). author reply 448PubMedCrossRef
68.
Zurück zum Zitat S. Cairo, Y. Wang, A. de Reynies, K. Duroure, J. Dahan, M.J. Redon et al., Stem cell-like micro-RNA signature driven by Myc in aggressive liver cancer. Proc. Natl. Acad. Sci. U.S.A. 107(47), 20471–20476 (2010)PubMedCrossRef S. Cairo, Y. Wang, A. de Reynies, K. Duroure, J. Dahan, M.J. Redon et al., Stem cell-like micro-RNA signature driven by Myc in aggressive liver cancer. Proc. Natl. Acad. Sci. U.S.A. 107(47), 20471–20476 (2010)PubMedCrossRef
69.
Zurück zum Zitat R.J. Isfort, D.B. Cody, C.J. Doersen, W.G. Richards, B.K. Yoder, J.E. Wilkinson et al., The tetratricopeptide repeat containing Tg737 gene is a liver neoplasia tumor suppressor gene. Oncogene 15(15), 1797–1803 (1997)PubMedCrossRef R.J. Isfort, D.B. Cody, C.J. Doersen, W.G. Richards, B.K. Yoder, J.E. Wilkinson et al., The tetratricopeptide repeat containing Tg737 gene is a liver neoplasia tumor suppressor gene. Oncogene 15(15), 1797–1803 (1997)PubMedCrossRef
70.
Zurück zum Zitat N. You, W. Liu, X. Zhong, R. Ji, M. Zhang, H. You et al., Tg737 inhibition results in malignant transformation in fetal liver stem/progenitor cells by promoting cell-cycle progression and differentiation arrest. Mol. Carcinog. 51(8), 659–673 (2012)PubMedCrossRef N. You, W. Liu, X. Zhong, R. Ji, M. Zhang, H. You et al., Tg737 inhibition results in malignant transformation in fetal liver stem/progenitor cells by promoting cell-cycle progression and differentiation arrest. Mol. Carcinog. 51(8), 659–673 (2012)PubMedCrossRef
71.
Zurück zum Zitat B. Zhang, X. Pan, G.P. Cobb, T.A. Anderson, microRNAs as oncogenes and tumor suppressors. Dev. Biol. 302(1), 1–12 (2007)PubMedCrossRef B. Zhang, X. Pan, G.P. Cobb, T.A. Anderson, microRNAs as oncogenes and tumor suppressors. Dev. Biol. 302(1), 1–12 (2007)PubMedCrossRef
72.
Zurück zum Zitat C.E. Rogler, MicroRNAs make inroads into liver development. Gastroenterology 136(3), 770–772 (2009)PubMedCrossRef C.E. Rogler, MicroRNAs make inroads into liver development. Gastroenterology 136(3), 770–772 (2009)PubMedCrossRef
73.
Zurück zum Zitat E.J. Lee, Y. Gusev, J. Jiang, G.J. Nuovo, M.R. Lerner, W.L. Frankel et al., Expression profiling identifies microRNA signature in pancreatic cancer. Int. J. Cancer 120(5), 1046–1054 (2007)PubMedCrossRef E.J. Lee, Y. Gusev, J. Jiang, G.J. Nuovo, M.R. Lerner, W.L. Frankel et al., Expression profiling identifies microRNA signature in pancreatic cancer. Int. J. Cancer 120(5), 1046–1054 (2007)PubMedCrossRef
74.
Zurück zum Zitat Q.W. Wong, R.W. Lung, P.T. Law, P.B. Lai, K.Y. Chan, K.F. To et al., MicroRNA-223 is commonly repressed in hepatocellular carcinoma and potentiates expression of Stathmin1. Gastroenterology 135(1), 257–269 (2008)PubMedCrossRef Q.W. Wong, R.W. Lung, P.T. Law, P.B. Lai, K.Y. Chan, K.F. To et al., MicroRNA-223 is commonly repressed in hepatocellular carcinoma and potentiates expression of Stathmin1. Gastroenterology 135(1), 257–269 (2008)PubMedCrossRef
75.
Zurück zum Zitat R. Liu, Z. Zhou, D. Zhao, C. Chen, The Induction of KLF5 Transcription Factor by Progesterone Contributes to Progesterone-Induced Breast Cancer Cell Proliferation and Dedifferentiation. Mol. Endocrinol. 25(7), 1137–1144 (2011)PubMedCrossRef R. Liu, Z. Zhou, D. Zhao, C. Chen, The Induction of KLF5 Transcription Factor by Progesterone Contributes to Progesterone-Induced Breast Cancer Cell Proliferation and Dedifferentiation. Mol. Endocrinol. 25(7), 1137–1144 (2011)PubMedCrossRef
76.
Zurück zum Zitat S. Chumsri, P. Phatak, M.J. Edelman, N. Khakpour, A.W. Hamburger, A.M. Burger, Cancer stem cells and individualized therapy. Cancer Genomics Proteomics 4(3), 165–174 (2007)PubMed S. Chumsri, P. Phatak, M.J. Edelman, N. Khakpour, A.W. Hamburger, A.M. Burger, Cancer stem cells and individualized therapy. Cancer Genomics Proteomics 4(3), 165–174 (2007)PubMed
77.
Zurück zum Zitat G. Federici, V. Espina, L. Liotta, K.H. Edmiston, Breast cancer stem cells: A new target for therapy. Oncology (Williston Park) 25(1), 25–28 (2011) G. Federici, V. Espina, L. Liotta, K.H. Edmiston, Breast cancer stem cells: A new target for therapy. Oncology (Williston Park) 25(1), 25–28 (2011)
78.
Zurück zum Zitat D. Dingli, F. Michor, Successful therapy must eradicate cancer stem cells. Stem Cells 24(12), 2603–2610 (2006)PubMedCrossRef D. Dingli, F. Michor, Successful therapy must eradicate cancer stem cells. Stem Cells 24(12), 2603–2610 (2006)PubMedCrossRef
79.
Zurück zum Zitat Y. Liu, W.L. Lu, J. Guo, J. Du, T. Li, J.W. Wu et al., A potential target associated with both cancer and cancer stem cells: a combination therapy for eradication of breast cancer using vinorelbine stealthy liposomes plus parthenolide stealthy liposomes. J. Control. Release 129(1), 18–25 (2008)PubMedCrossRef Y. Liu, W.L. Lu, J. Guo, J. Du, T. Li, J.W. Wu et al., A potential target associated with both cancer and cancer stem cells: a combination therapy for eradication of breast cancer using vinorelbine stealthy liposomes plus parthenolide stealthy liposomes. J. Control. Release 129(1), 18–25 (2008)PubMedCrossRef
80.
Zurück zum Zitat J. Gil, A. Stembalska, K.A. Pesz, M.M. Sasiadek, Cancer stem cells: The theory and perspectives in cancer therapy. J. Appl. Genet. 49(2), 193–199 (2008)PubMedCrossRef J. Gil, A. Stembalska, K.A. Pesz, M.M. Sasiadek, Cancer stem cells: The theory and perspectives in cancer therapy. J. Appl. Genet. 49(2), 193–199 (2008)PubMedCrossRef
81.
Zurück zum Zitat L. Milas, W.N. Hittelman, Cancer stem cells and tumor response to therapy: current problems and future prospects. Semin. Radiat. Oncol. 19(2), 96–105 (2009)PubMedCrossRef L. Milas, W.N. Hittelman, Cancer stem cells and tumor response to therapy: current problems and future prospects. Semin. Radiat. Oncol. 19(2), 96–105 (2009)PubMedCrossRef
82.
Zurück zum Zitat Y.L. Hu, Y.H. Fu, Y. Tabata, J.Q. Gao, Mesenchymal stem cells: a promising targeted-delivery vehicle in cancer gene therapy. J. Control. Release 147(2), 154–162 (2010)PubMedCrossRef Y.L. Hu, Y.H. Fu, Y. Tabata, J.Q. Gao, Mesenchymal stem cells: a promising targeted-delivery vehicle in cancer gene therapy. J. Control. Release 147(2), 154–162 (2010)PubMedCrossRef
83.
Zurück zum Zitat P. Aimola, V. Desiderio, A. Graziano, P.P. Claudio, Stem cells in cancer therapy: From their role in pathogenesis to their use as therapeutic agents. Drug News Perspect. 23(3), 175–183 (2010)PubMedCrossRef P. Aimola, V. Desiderio, A. Graziano, P.P. Claudio, Stem cells in cancer therapy: From their role in pathogenesis to their use as therapeutic agents. Drug News Perspect. 23(3), 175–183 (2010)PubMedCrossRef
84.
Zurück zum Zitat R. Uchibori, K. Ozawa, [Mesenchymal stem cells (MSCs) as a platform for cancer gene therapy]. Rinsho Ketsueki 51(11), 1641–1646 (2010)PubMed R. Uchibori, K. Ozawa, [Mesenchymal stem cells (MSCs) as a platform for cancer gene therapy]. Rinsho Ketsueki 51(11), 1641–1646 (2010)PubMed
85.
Zurück zum Zitat L.J. Dai, M.R. Moniri, Z.R. Zeng, J.X. Zhou, J. Rayat, G.L. Warnock, Potential implications of mesenchymal stem cells in cancer therapy. Cancer Lett. 305(1), 8–20 (2011)PubMedCrossRef L.J. Dai, M.R. Moniri, Z.R. Zeng, J.X. Zhou, J. Rayat, G.L. Warnock, Potential implications of mesenchymal stem cells in cancer therapy. Cancer Lett. 305(1), 8–20 (2011)PubMedCrossRef
86.
Zurück zum Zitat K. Shah, Mesenchymal stem cells engineered for cancer therapy. Adv. Drug Deliv. Rev. 64(8), 739–748 (2012)PubMedCrossRef K. Shah, Mesenchymal stem cells engineered for cancer therapy. Adv. Drug Deliv. Rev. 64(8), 739–748 (2012)PubMedCrossRef
87.
Zurück zum Zitat I.S. Florian, C. Tomuleasa, O. Soritau, T. Timis, H. Ioani, A. Irimie et al., Cancer stem cells and malignant gliomas. From pathophysiology to targeted molecular therapy. J. BUON 16(1), 16–23 (2011)PubMed I.S. Florian, C. Tomuleasa, O. Soritau, T. Timis, H. Ioani, A. Irimie et al., Cancer stem cells and malignant gliomas. From pathophysiology to targeted molecular therapy. J. BUON 16(1), 16–23 (2011)PubMed
88.
Zurück zum Zitat H. Beug, Breast cancer stem cells: eradication by differentiation therapy? Cell 138(4), 623–625 (2009)PubMedCrossRef H. Beug, Breast cancer stem cells: eradication by differentiation therapy? Cell 138(4), 623–625 (2009)PubMedCrossRef
89.
Zurück zum Zitat L. Wijaya, D. Agustina, A.O. Lizandi, M.M. Kartawinata, F. Sandra, Reversing breast cancer stem cell into breast somatic stem cell. Curr. Pharm. Biotechnol. 12(2), 189–195 (2011)PubMedCrossRef L. Wijaya, D. Agustina, A.O. Lizandi, M.M. Kartawinata, F. Sandra, Reversing breast cancer stem cell into breast somatic stem cell. Curr. Pharm. Biotechnol. 12(2), 189–195 (2011)PubMedCrossRef
90.
Zurück zum Zitat F.A. Kruyt, J.J. Schuringa, Apoptosis and cancer stem cells: Implications for apoptosis targeted therapy. Biochem. Pharmacol. 80(4), 423–430 (2010)PubMedCrossRef F.A. Kruyt, J.J. Schuringa, Apoptosis and cancer stem cells: Implications for apoptosis targeted therapy. Biochem. Pharmacol. 80(4), 423–430 (2010)PubMedCrossRef
91.
Zurück zum Zitat S. Sell, Potential gene therapy strategies for cancer stem cells. Curr. Gene Ther. 6(5), 579–591 (2006)PubMedCrossRef S. Sell, Potential gene therapy strategies for cancer stem cells. Curr. Gene Ther. 6(5), 579–591 (2006)PubMedCrossRef
92.
Zurück zum Zitat S. Soltanian, M.M. Matin, Cancer stem cells and cancer therapy. Tumour Biol. 32(3), 425–440 (2011)PubMedCrossRef S. Soltanian, M.M. Matin, Cancer stem cells and cancer therapy. Tumour Biol. 32(3), 425–440 (2011)PubMedCrossRef
93.
Zurück zum Zitat O.K. Okamoto, J.F. Perez, Targeting cancer stem cells with monoclonal antibodies: a new perspective in cancer therapy and diagnosis. Expert Rev. Mol. Diagn. 8(4), 387–393 (2008)PubMedCrossRef O.K. Okamoto, J.F. Perez, Targeting cancer stem cells with monoclonal antibodies: a new perspective in cancer therapy and diagnosis. Expert Rev. Mol. Diagn. 8(4), 387–393 (2008)PubMedCrossRef
94.
Zurück zum Zitat M.R. Alison, S.M. Lim, L.J. Nicholson, Cancer stem cells: problems for therapy? J. Pathol. 223(2), 147–161 (2011)PubMedCrossRef M.R. Alison, S.M. Lim, L.J. Nicholson, Cancer stem cells: problems for therapy? J. Pathol. 223(2), 147–161 (2011)PubMedCrossRef
95.
Zurück zum Zitat E. Gorelik, A. Lokshin, V. Levina, Lung cancer stem cells as a target for therapy. Anticancer Agents Med Chem. 10(2), 164–171 (2010)PubMedCrossRef E. Gorelik, A. Lokshin, V. Levina, Lung cancer stem cells as a target for therapy. Anticancer Agents Med Chem. 10(2), 164–171 (2010)PubMedCrossRef
96.
Zurück zum Zitat G.J. Leiros, M.E. Balana, Metastatic cancer stem cells: new molecular targets for cancer therapy. Curr. Pharm. Biotechnol. 12(11), 1909–1922 (2011)PubMedCrossRef G.J. Leiros, M.E. Balana, Metastatic cancer stem cells: new molecular targets for cancer therapy. Curr. Pharm. Biotechnol. 12(11), 1909–1922 (2011)PubMedCrossRef
97.
Zurück zum Zitat M.E. Sehl, J.S. Sinsheimer, H. Zhou, K.L. Lange, Differential destruction of stem cells: implications for targeted cancer stem cell therapy. Cancer Res. 69(24), 9481–9489 (2009)PubMedCrossRef M.E. Sehl, J.S. Sinsheimer, H. Zhou, K.L. Lange, Differential destruction of stem cells: implications for targeted cancer stem cell therapy. Cancer Res. 69(24), 9481–9489 (2009)PubMedCrossRef
Metadaten
Titel
Interpretation of interlocking key issues of cancer stem cells in malignant solid tumors
verfasst von
Wei-hui Liu
Nan You
Ning Zhang
Hong-tao Yan
Tao Wang
Zhu Huang
Hong-bao Liu
Li-jun Tang
Publikationsdatum
01.12.2012
Verlag
Springer Netherlands
Erschienen in
Cellular Oncology / Ausgabe 6/2012
Print ISSN: 2211-3428
Elektronische ISSN: 2211-3436
DOI
https://doi.org/10.1007/s13402-012-0110-8

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