ChunJiao Song, Huan Chen, ChaoYang Xu, GuoMei Ru
Shaoxing People's Hospital, Shaoxing Hospital of Zhejiang University, Shaoxing, Zhejiang Province, China.
IUBMB Life. 2014 Jun;66(6):379-86. doi: 10.1002/iub.1281. Epub 2014 Jun 30.
Prostate cancer (PCa) is the second most commonly occurring malignant tumor in Europe and America. Normal and neoplastic growth of prostate gland are dependent on androgen receptor (AR) expression and function. PCa is driven by androgen and its receptor, and they continue to be the key drivers of castration-resistant prostate cancer (CRPC). CRPC is the terminal stage of PCa and seriously jeopardizes the patient's quality of life and lifespan. miRNAs are small noncoding RNAs, 18-25 nt in length that destabilize mRNA or repress protein synthesis by interacting with the 3'-untranslated regions (3'-UTR) of target mRNAs. miRNAs can regulate AR or be regulated by AR and then affect various signaling pathways related to cellular functions and tumor processes. In this review, we focus on the relationship between miRNAs and AR in PCa and elucidate their roles in the induction of malignant changes in PCa.
前列腺癌(PCa)是欧美地区第二常见的恶性肿瘤。前列腺的正常生长和肿瘤生长依赖于雄激素受体(AR)的表达和功能。PCa由雄激素及其受体驱动,它们仍然是去势抵抗性前列腺癌(CRPC)的关键驱动因素。CRPC是PCa的终末期,严重危及患者的生活质量和寿命。微小RNA(miRNA)是长度为18 - 25个核苷酸的小型非编码RNA,通过与靶mRNA的3'非翻译区(3'-UTR)相互作用使mRNA不稳定或抑制蛋白质合成。miRNA可以调节AR或受AR调节,进而影响与细胞功能和肿瘤进程相关的各种信号通路。在本综述中,我们聚焦于PCa中miRNA与AR的关系,并阐明它们在PCa恶性变化诱导中的作用。