Therapeutic Strategies for Targeting Ovarian Cancer Stem Cells

被引:22
|
作者
Yang, Wookyeom [1 ]
Kim, Dasol [2 ]
Kim, Dae Kyoung [2 ]
Choi, Kyung Un [3 ]
Suh, Dong Soo [4 ]
Kim, Jae Ho [2 ]
机构
[1] Pusan Natl Univ, Convergence Stem Cell Res Ctr, Yangsan 50612, Gyeongsangnam D, South Korea
[2] Pusan Natl Univ, Sch Med, Dept Physiol, Yangsan 50612, Gyeongsangnam D, South Korea
[3] Pusan Natl Univ Hosp, Dept Pathol, Busan 49241, South Korea
[4] Pusan Natl Univ Hosp, Dept Obstet & Gynecol, Busan 49241, South Korea
基金
新加坡国家研究基金会;
关键词
cancer stem cells; ovarian cancer; chemoreistance; stemess; HUMAN ADIPOSE-TISSUE; INDEPENDENT PROGNOSTIC MARKER; DRUG-RESISTANCE ROLE; LYSOPHOSPHATIDIC ACID; EMBRYONIC STEM; ALDEHYDE DEHYDROGENASE; INITIATING CELLS; POOR-PROGNOSIS; SOLID TUMORS; LYSOPHOSPHOLIPASE-D;
D O I
10.3390/ijms22105059
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ovarian cancer is a fatal gynecological malignancy. Although first-line chemotherapy and surgical operation are effective treatments for ovarian cancer, its clinical management remains a challenge owing to intrinsic or acquired drug resistance and relapse at local or distal lesions. Cancer stem cells (CSCs) are a small subpopulation of cells inside tumor tissues, and they can self-renew and differentiate. CSCs are responsible for the cancer malignancy involved in relapses as well as resistance to chemotherapy and radiation. These malignant properties of CSCs are regulated by cell surface receptors and intracellular pluripotency-associated factors triggered by internal or external stimuli from the tumor microenvironment. The malignancy of CSCs can be attenuated by individual or combined restraining of cell surface receptors and intracellular pluripotency-associated factors. Therefore, targeted therapy against CSCs is a feasible therapeutic tool against ovarian cancer. In this paper, we review the prominent roles of cell surface receptors and intracellular pluripotency-associated factors in mediating the stemness and malignancy of ovarian CSCs.
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收藏
页数:17
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