New insights into prostate cancer stem cells

被引:69
|
作者
Chen, Xin [1 ]
Rycaj, Kiera [1 ]
Liu, Xin [1 ,2 ]
Tang, Dean G. [1 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Mol Carcinogenesis, Smithville, TX 78957 USA
[2] Univ Texas Austin, Dept Nutr Sci, Austin, TX 78712 USA
[3] Univ Texas MD Anderson Canc Ctr, Ctr Canc Epigenet Stem Cell & Dev Biol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Ctr RNA Interference & Noncoding RNAs, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Ctr Mol Carcinogenesis, Houston, TX 77030 USA
[6] Tongji Univ, Sch Med, East Hosp, Canc Stem Cell Inst,Res Ctr Translat Med, Shanghai 200092, Peoples R China
关键词
prostate cancer; cancer stem cells; prostate cancer stem cells; differentiation; therapy resistance; EPITHELIAL BASAL-CELLS; ACUTE MYELOID-LEUKEMIA; SELF-RENEWAL; INITIATING CELLS; TUMOR-GROWTH; PROSPECTIVE IDENTIFICATION; ALDEHYDE DEHYDROGENASE; STEM/PROGENITOR CELLS; MOLECULAR-GENETICS; SIDE-POPULATION;
D O I
10.4161/cc.23721
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prostate cancer (PCa) remains one of the most prevalent malignancies affecting men in the western world. The etiology for PCa development and molecular mechanisms underlying castration-resistant progression are incompletely understood. Emerging evidence from many tumor systems has shown the existence of distinct subpopulations of stem like-cancer cells termed cancer stem cells (CSCs), which may be involved in tumor initiation, progression, metastasis and therapy resistance. Prostate cancer stem cells (PCSCs) have also been identified using different experimental strategies in distinct model systems. In this brief review, we summarize our current knowledge of normal prostate stem/progenitor cells, highlight recent progress on PCSCs, expound on the potential cell of origin for PCa and discuss the involvement of PCSCs in PCa progression and castration resistance. Elucidation of the phenotypic and functional properties and molecular regulation of PCSCs will help us better understand PCa biology and may lead to development of novel therapeutics targeting castration-resistant PCa cells.
引用
收藏
页码:579 / 586
页数:8
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