- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
BioMed Research International
Volume 2013 (2013), Article ID 510905, 11 pages
Ovarian and Breast Cancer Spheres Are Similar in Transcriptomic Features and Sensitive to Fenretinide
1Key Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS) and Shanghai Jiao Tong University School of Medicine (SJTU-SM), 225 Chong-Qing South Road, Shanghai 200025, China
2Graduate School of the Chinese Academy of Sciences, Beijing 100049, China
Received 17 April 2013; Revised 16 August 2013; Accepted 18 August 2013
Academic Editor: George Perry
Copyright © 2013 Haiwei Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- D. Bonnet and J. E. Dick, “Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell,” Nature Medicine, vol. 3, no. 7, pp. 730–737, 1997.
- M. Al-Hajj, M. S. Wicha, A. Benito-Hernandez, S. J. Morrison, and M. F. Clarke, “Prospective identification of tumorigenic breast cancer cells,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 7, pp. 3983–3988, 2003.
- S. K. Singh, C. Hawkins, I. D. Clarke et al., “Identification of human brain tumour initiating cells,” Nature, vol. 432, no. 7015, pp. 396–401, 2004.
- C. A. O'Brien, A. Pollett, S. Gallinger, and J. E. Dick, “A human colon cancer cell capable of initiating tumour growth in immunodeficient mice,” Nature, vol. 445, no. 7123, pp. 106–110, 2007.
- P. C. Hermann, S. L. Huber, T. Herrler et al., “Distinct populations of cancer stem cells determine tumor growth and metastatic activity in human pancreatic cancer,” Cell Stem Cell, vol. 1, no. 3, pp. 313–323, 2007.
- S. Zhang, C. Balch, M. W. Chan et al., “Identification and characterization of ovarian cancer-initiating cells from primary human tumors,” Cancer Research, vol. 68, no. 11, pp. 4311–4320, 2008.
- R. Bjerkvig, B. B. Tysnes, K. S. Aboody, J. Najbauer, and A. J. A. Terzis, “The origin of the cancer stem cell: current controversies and new insights,” Nature Reviews Cancer, vol. 5, no. 11, pp. 899–904, 2005.
- M. Diehn, R. W. Cho, N. A. Lobo et al., “Association of reactive oxygen species levels and radioresistance in cancer stem cells,” Nature, vol. 458, no. 7239, pp. 780–783, 2009.
- P. B. Gupta, T. T. Onder, G. Jiang et al., “Identification of selective inhibitors of cancer stem cells by high-throughput screening,” Cell, vol. 138, no. 4, pp. 645–659, 2009.
- D. Burgos-Ojeda, B. R. Rueda, and R. J. Buckanovich, “Ovarian cancer stem cell markers: prognostic and therapeutic implications,” Cancer Letters, vol. 311, no. 1, pp. 1–7, 2012.
- G. Dontu, W. M. Abdallah, J. M. Foley et al., “In vitro propagation and transcriptional profiling of human mammary stem/progenitor cells,” Genes and Development, vol. 17, no. 10, pp. 1253–1270, 2003.
- L. Ricci-Vitiani, D. G. Lombardi, E. Pilozzi et al., “Identification and expansion of human colon-cancer-initiating cells,” Nature, vol. 445, no. 7123, pp. 111–115, 2007.
- Z. Su, W. S. Graybill, and Y. Zhu, “Detection and monitoring of ovarian cancer,” Clinica Chimica Acta, vol. 415, pp. 341–345, 2013.
- M. C. King, J. H. Marks, and J. B. Mandell, “Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2,” Science, vol. 302, no. 5645, pp. 643–646, 2003.
- D. J. Slamon, W. Godolphin, L. A. Jones et al., “Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer,” Science, vol. 244, no. 4905, pp. 707–712, 1989.
- P. E. Schwartz, J. T. Chambers, E. I. Kohorn et al., “Tamoxifen in combination with cytotoxic chemotherapy in advanced epithelial ovarian cancer. A prospective randomized trial,” Cancer, vol. 63, no. 6, pp. 1074–1078, 1989.
- A. Latifi, K. Abubaker, N. Castrechini et al., “Cisplatin treatment of primary and metastatic epithelial ovarian carcinomas generates residual cells with mesenchymal stem cell-like profile,” Journal of Cellular Biochemistry, vol. 112, no. 10, pp. 2850–2864, 2011.
- E. Ulukaya and E. J. Wood, “Fenretinide and its relation to cancer,” Cancer Treatment Reviews, vol. 25, no. 4, pp. 229–235, 1999.
- W. Malone, M. Perloff, J. Crowell, C. Sigman, and H. Higley, “Fenretinide: a prototype cancer prevention drug,” Expert Opinion on Investigational Drugs, vol. 12, no. 11, pp. 1829–1842, 2003.
- P. E. Lovat, M. Ranalli, M. Corazzari et al., “Mechanisms of free-radical induction in relation to fenretinide-induced apoptosis of neuroblastoma,” Journal of Cellular Biochemistry, vol. 89, no. 4, pp. 698–708, 2003.
- N. Hail Jr., H. J. Kim, and R. Lotan, “Mechanisms of fenretinide-induced apoptosis,” Apoptosis, vol. 11, no. 10, pp. 1677–1694, 2006.
- Y. Du, Y. Xia, X. Pan, et al., “Fenretinide targets chronic myeloid leukemia stem/progenitor cells by regulation of redox signaling,” Antioxidants and Redox Signaling, 2013.
- The Gene Ontology Consortium, “The gene ontology project in 2008,” Nucleic Acids Research, vol. 36, supplement 1, pp. D440–D444, 2008.
- W. Miller, K. Rosenbloom, R. C. Hardison et al., “28-Way vertebrate alignment and conservation track in the UCSC genome browser,” Genome Research, vol. 17, no. 12, pp. 1797–1808, 2007.
- N. Yoshizumi, J. Fujiwara, A. Yoshizaki, M. Sato, R. Sakai, and I. Nishiya, “Cytokinetic effects of carboplatin and cisplatin on a human ovarian cancer cell line,” Human Cell, vol. 1, no. 3, pp. 301–307, 1988.
- V. Vathipadiekal, D. Saxena, S. C. Mok, P. V. Hauschka, L. Ozbun, and M. J. Birrer, “Identification of a potential ovarian cancer stem cell gene expression profile from advanced stage papillary serous ovarian cancer,” PLoS ONE, vol. 7, no. 1, Article ID e29079, 2012.
- C. K. McCann, W. B. Growdon, K. Kulkarni-Datar et al., “Inhibition of hedgehog signaling antagonizes serous ovarian cancer growth in a primary xenograft model,” PLoS ONE, vol. 6, no. 11, Article ID e28077, 2011.
- M. Wickstrom, C. Dyberg, T. Shimokawa et al., “Targeting the hedgehog signal transduction pathway at the level of GLI inhibits neuroblastoma cell growth in vitro and in vivo,” International Journal of Cancer, vol. 132, no. 7, pp. 1516–1524, 2013.
- A. D. Steg, K. S. Bevis, A. A. Katre et al., “Stem cell pathways contribute to clinical chemoresistance in ovarian cancer,” Clinical Cancer Research, vol. 18, no. 3, pp. 869–881, 2012.
- N. Y. Frank, A. Margaryan, Y. Huang et al., “ABCB5-mediated doxorubicin transport and chemoresistance in human malignant melanoma,” Cancer Research, vol. 65, no. 10, pp. 4320–4333, 2005.
- K. M. Britton, R. Eyre, I. J. Harvey et al., “Breast cancer, side population cells and ABCG2 expression,” Cancer Letters, vol. 323, no. 1, pp. 97–105, 2012.
- M. J. Grimshaw, L. Cooper, K. Papazisis et al., “Mammosphere culture of metastatic breast cancer cells enriches for tumorigenic breast cancer cells,” Breast Cancer Research, vol. 10, no. 3, article R52, 2008.
- C. Ginestier, M. H. Hur, E. Charafe-Jauffret et al., “ALDH1 is a marker of normal and malignant human mammary stem cells and a predictor of poor clinical outcome,” Cell Stem Cell, vol. 1, no. 5, pp. 555–567, 2007.
- M. Heuser, L. M. Sly, B. Argiropoulos et al., “Modeling the functional heterogeneity of leukemia stem cells: role of STAT5 in leukemia stem cell self-renewal,” Blood, vol. 114, no. 19, pp. 3983–3993, 2009.
- L. Y. W. Bourguignon, K. Peyrollier, W. Xia, and E. Gilad, “Hyaluronan-CD44 interaction activates stem cell marker Nanog, Stat-3-mediated MDR1 gene expression, and ankyrin-regulated multidrug efflux in breast and ovarian tumor cells,” The Journal of Biological Chemistry, vol. 283, no. 25, pp. 17635–17651, 2008.
- J. Wu, J. P. Williams, T. A. Rizvi et al., “Plexiform and dermal neurofibromas and pigmentation are caused by Nf1 loss in desert hedgehog-expressing cells,” Cancer Cell, vol. 13, no. 2, pp. 105–116, 2008.
- E. E. Ibrahim, R. Babaei-Jadidi, A. Saadeddin et al., “Embryonic NANOG activity defines colorectal cancer stem cells and modulates through AP1- and TCF-dependent mechanisms,” Stem Cells, vol. 30, no. 10, pp. 2076–2087.
- H. Zhang, J. Q. Mi, H. Fang et al., “Preferential eradication of acute myelogenous leukemia stem cells by fenretinide,” Proceedings of the National Academy of Sciences of the United States of America, vol. 110, no. 14, pp. 5606–5611.
- U. Veronesi, G. de Palo, E. Marubini et al., “Randomized trial of fenretinide to prevent second breast malignancy in women with early breast cancer,” Journal of the National Cancer Institute, vol. 91, no. 21, pp. 1847–1856, 1999.
- D. Trachootham, J. Alexandre, and P. Huang, “Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach?” Nature Reviews Drug Discovery, vol. 8, no. 7, pp. 579–591, 2009.
- N. Oridate, S. Suzuki, M. Higuchi, M. F. Mitchell, W. K. Hong, and R. Lotan, “Involvement of reactive oxygen species in N-(4-hydroxyphenyl)retinamide-induced apoptosis in cervical carcinoma cells,” Journal of the National Cancer Institute, vol. 89, no. 16, pp. 1191–1198, 1997.
- K. Wang, H. Fang, D. Xiao et al., “Converting redox signaling to apoptotic activities by stress-responsive regulators HSF1 and NRF2 in fenretinide treated cancer cells,” PLoS ONE, vol. 4, no. 10, Article ID e7538, 2009.
- L. Jiang, X. Pan, Y. Chen, K. Wang, Y. Du, and J. Zhang, “Preferential involvement of both ROS and ceramide in fenretinide-induced apoptosis of HL60 rather than NB4 and U937 cells,” Biochemical and Biophysical Research Communications, vol. 405, no. 2, pp. 314–318, 2011.
- Y. H. Yu, G. Y. Chiou, P. I. Huang et al., “Network biology of tumor stem-like cells identified a regulatory role of CBX5 in lung cancer,” Scientific Reports, vol. 2, article 584, 2012.
- C. Tringali, F. Cirillo, G. Lamorte et al., “NEU4L sialidase overexpression promotes β-catenin signaling in neuroblastoma cells, enhancing stem-like malignant cell growth,” International Journal of Cancer, vol. 131, no. 8, pp. 1768–1778, 2012.