The role of microRNA in castration-resistant prostate cancer

被引:35
作者
Thieu, William
Tilki, Derya
White, Ralph W. deVere
Evans, Christopher P. [1 ]
机构
[1] Univ Calif Davis, Med Ctr, Dept Urol, Sacramento, CA 95817 USA
关键词
Castration-resistant prostate cancer; microRNA; Review; ANDROGEN RECEPTOR; E-CADHERIN; TAMOXIFEN RESISTANCE; TRAIL RESISTANCE; BREAST-CANCER; RHO-GTPASE; C-MYC; EXPRESSION; ACTIVATION; TARGETS;
D O I
10.1016/j.urolonc.2013.11.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Castration-resistant prostate cancer (CRPC) has a historically low median survival rate, but recent advances and discoveries in microRNAs (miRNAs) have opened the potential for new prognostication modalities to enhance therapeutic success. As new chemotherapies and immunotherapies are developed, there is an increasing need for precision and stratification of CRPC to allow for optimization and personalization of therapy. Methods: A systematic literature review was conducted via electronic database resulting in the selection of 42 articles based on title, abstract, study format, and content by a consensus of all participating authors. Most selected articles were published between 2002 and 2013. In this review, we discuss the robustness of miRNAs as a biomarker platform, miRNAs associated with prostate cancer, and recent discoveries of miRNA associations with CRPC. Results: The associations discovered have been of interest owing to the ability to differentiate between CRPC and localized prostate cancer. With the evaluation of multiple miRNAs, it is possible to provide a profile regarding tumor characteristics. Furthermore, actions of miRNAs on CRPC tumor cells have the ability to suppress metastatic phenotypes. Conclusion: miRNAs may have a growing role in CRPC prognostication and may potentially transform into a therapeutic potential. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:517 / 523
页数:7
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