Xu Shaohua, Wang Tao, Song Wen, Jiang Tao, Zhang Feng, Yin Yu, Jiang Shi-Wen, Wu Kongming, Yu Zuoren, Wang Chenguang, Chen Ke
Department of Gynecology, Shanghai First Matenity and Infant Hospital, Tongji University School of Medicine, Shanghai, China.
Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Sci Rep. 2015 Aug 28;5:13528. doi: 10.1038/srep13528.
Prostate cancer at advanced stages including metastatic and castration-resistant cancer remains incurable due to the lack of effective therapies. MiR-190a belongs to the small noncoding RNA family and has an important role in breast cancer metastasis. However, it is still unknown whether miR-190a plays a role in prostate cancer development. Herein, we first observed AR/miR-190a/YB-1 forms an auto-regulatory negative feedback loop in prostate cancer: miR-190a expression was down-regulated by AR activation; YB-1 functions are as an AR activator; miR-190a inhibited AR expression and transactivation through direct binding to 3'UTR of YB-1 gene. MiR-190a contributes the human prostate cancer cell growth through AR-dependent signaling. Moreover, we examined the expression of miR-190a and observed a significant decrease in human prostate cancers. Reduced expression of miR-190a was inversely correlated to AR levels of prostate cancer patients, and patients with higher miR-190a expression in their tumor have improved tumor-free survival. Taken together, our findings identified a biochemical and functional link between miR-190a with reduced expression in advanced prostate cancer, YB-1 and AR signaling in prostate cancer.
包括转移性和去势抵抗性癌症在内的晚期前列腺癌由于缺乏有效的治疗方法而仍然无法治愈。MiR-190a属于小非编码RNA家族,在乳腺癌转移中起重要作用。然而,miR-190a是否在前列腺癌发展中发挥作用仍不清楚。在此,我们首先观察到AR/miR-190a/YB-1在前列腺癌中形成一个自调节负反馈环:AR激活下调miR-190a表达;YB-1作为AR激活剂发挥作用;miR-190a通过直接结合YB-1基因的3'UTR抑制AR表达和反式激活。MiR-190a通过AR依赖信号促进人前列腺癌细胞生长。此外,我们检测了miR-190a的表达,发现其在人前列腺癌中显著降低。miR-190a表达降低与前列腺癌患者的AR水平呈负相关,肿瘤中miR-190a表达较高的患者无瘤生存期得到改善。综上所述,我们的研究结果确定了晚期前列腺癌中表达降低的miR-190a、YB-1和前列腺癌中的AR信号之间的生化和功能联系。