Stem and progenitor-like cells contribute to the aggressive behavior of human epithelial ovarian cancer
- PMID: 15833827
- DOI: 10.1158/0008-5472.CAN-04-3931
Stem and progenitor-like cells contribute to the aggressive behavior of human epithelial ovarian cancer
Abstract
The cellular mechanisms underlying the increasing aggressiveness associated with ovarian cancer progression are poorly understood. Coupled with a lack of identification of specific markers that could aid early diagnoses, the disease becomes a major cause of cancer-related mortality in women. Here we present direct evidence that the aggressiveness of human ovarian cancer may be a result of transformation and dysfunction of stem cells in the ovary. A single tumorigenic clone was isolated among a mixed population of cells derived from the ascites of a patient with advanced ovarian cancer. During the course of the study, yet another clone underwent spontaneous transformation in culture, providing a model of disease progression. Both the transformed clones possess stem cell-like characteristics and differentiate to grow in an anchorage-independent manner in vitro as spheroids, although further maturation and tissue-specific differentiation was arrested. Significantly, tumors established from these clones in animal models are similar to those in the human disease in their histopathology and cell architecture. Furthermore, the tumorigenic clones, even on serial transplantation continue to establish tumors, thereby confirming their identity as tumor stem cells. These findings suggest that: (a) stem cell transformation can be the underlying cause of ovarian cancer and (b) continuing stochastic events of stem and progenitor cell transformation define the increasing aggression that is characteristically associated with the disease.
Similar articles
-
Tumorigenic heterogeneity in cancer stem cells evolved from long-term cultures of telomerase-immortalized human mesenchymal stem cells.Cancer Res. 2005 Apr 15;65(8):3126-35. doi: 10.1158/0008-5472.CAN-04-2218. Cancer Res. 2005. PMID: 15833842
-
Isolation and characterization of human gastric cell lines with stem cell phenotypes.J Gastroenterol Hepatol. 2007 Sep;22(9):1460-8. doi: 10.1111/j.1440-1746.2007.05031.x. Epub 2007 Jul 20. J Gastroenterol Hepatol. 2007. PMID: 17645461
-
Niche-dependent tumorigenic capacity of malignant ovarian ascites-derived cancer cell subpopulations.Clin Cancer Res. 2009 Jan 1;15(1):70-80. doi: 10.1158/1078-0432.CCR-08-1233. Clin Cancer Res. 2009. PMID: 19118034
-
Molecular pathogenesis and therapeutic targets in epithelial ovarian cancer.J Cell Biochem. 2007 Dec 1;102(5):1117-29. doi: 10.1002/jcb.21552. J Cell Biochem. 2007. PMID: 17879946 Review.
-
Pathophysiological dynamics of human ovarian surface epithelial cells in epithelial ovarian carcinogenesis.Int Rev Cytol. 2005;242:1-54. doi: 10.1016/S0074-7696(04)42001-4. Int Rev Cytol. 2005. PMID: 15598466 Review.
Cited by
-
Targeting CD133 in an in vivo ovarian cancer model reduces ovarian cancer progression.Gynecol Oncol. 2013 Sep;130(3):579-87. doi: 10.1016/j.ygyno.2013.05.027. Epub 2013 May 27. Gynecol Oncol. 2013. PMID: 23721800 Free PMC article.
-
Isolation and identification of cancer stem-like cells from side population of human prostate cancer cells.J Huazhong Univ Sci Technolog Med Sci. 2012 Oct;32(5):697-703. doi: 10.1007/s11596-012-1020-8. Epub 2012 Oct 18. J Huazhong Univ Sci Technolog Med Sci. 2012. PMID: 23073799
-
Cancer Stem Cells: Detection and Characterization from Solid Tumors.Methods Mol Biol. 2024;2835:215-228. doi: 10.1007/978-1-0716-3995-5_18. Methods Mol Biol. 2024. PMID: 39105918
-
Target-specific delivery of doxorubicin to retinoblastoma using epithelial cell adhesion molecule aptamer.Mol Vis. 2012;18:2783-95. Epub 2012 Nov 22. Mol Vis. 2012. PMID: 23213278 Free PMC article.
-
The effect of salinomycin on ovarian cancer stem-like cells.Obstet Gynecol Sci. 2016 Jul;59(4):261-8. doi: 10.5468/ogs.2016.59.4.261. Epub 2016 Jul 13. Obstet Gynecol Sci. 2016. PMID: 27462592 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical