Ovarian cancer stem cells: Working towards the root of sternness

被引:111
作者
Foster, Rosemary [1 ,2 ]
Buckanovich, Ronald J. [3 ,4 ,5 ]
Rueda, Bo R. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Dept Obstet & Gynecol, Vincent Ctr Reprod Biol, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Obstet & Gynecol, Div Gynecol Oncol, Boston, MA 02114 USA
[3] Univ Michigan, Cell & Mol Biol Program, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Obstet & Gynecol, Ann Arbor, MI 48109 USA
关键词
Cancer stem cells; Ovarian cancer; SIDE-POPULATION CELLS; ALDEHYDE DEHYDROGENASE; BREAST-CANCER; INITIATING CELLS; FALLOPIAN-TUBE; EXPRESSION; IDENTIFICATION; CD133; CHEMOTHERAPY; PATHOGENESIS;
D O I
10.1016/j.canlet.2012.10.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Despite medical advances made over the past decade, ovarian cancer remains one of the more lethal gynecologic cancers in the United States. While current therapeutic strategies are relatively effective, there is a high incidence of recurrent chemoresistant disease. This has been attributed, in part, to a regenerative tumor cell sub-population that has acquired stem cell properties which allows these cells to escape standard chemotherapeutics and drive recurrent disease. To date, a number of laboratories have identified these cancer stem cell (CSC) sub-populations in ovarian cancer cell lines, tumors or ascites and the collective findings suggest ovarian CSCs are likely to be as heterogeneous as the disease itself. Moreover, the multiple ovarian histophenotypes and possible sites of disease origin together with the potential for differential hierarchal contributions of multiple CSCs populations represent significant challenges to the identification, functional characterization and therapeutic targeting of ovarian CSC. This review will highlight the markers and methodology currently used to identify and isolate these cells. We will discuss some of the underlying ovarian CSC biology, the signaling pathways implicated in their survival, replication and differentiation and potential therapeutic targeting strategies. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:147 / 157
页数:11
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