Wei Yongbao, Yang Jinrui, Yi Lu, Wang Yinhuai, Dong Zhitao, Liu Ziting, Ou-yang Shifeng, Wu Hongtao, Zhong Zhaohui, Yin Zhuo, Zhou Keqin, Gao Yunliang, Yan Bin, Wang Zhao
Department of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Sci Rep. 2014 Dec 18;4:7546. doi: 10.1038/srep07546.
MicroRNAs (miRNAs) present frequently altered expression in urologic cancers including prostate, bladder, and kidney cancer. The altered expression of miR-223 has been reported in cancers and other diseases in recent researches. MiR-223 is up-regulated in systemic lupus erythematosus and rheumatoid arthritis. In neoplastic diseases, miR-223 is proved to be up-expressed in plasma or serum and cancer tissues compared with normal tissues in pancreatic cancer, gastric cancer, et al. However, whether altered expression of miR-223 is associated with prostate cancer (PCa) and what it is potential functions in PCa remained unveiled. In this study, we firstly found miR-223-3p were up-regulated in prostate cancer tissues and then we study functional role of miR-223-3p in PCa using DU145, PC3 and LNCaP cell lines. Our data suggested that miR-223-3p might target gene SEPT6 and promoted the biological behavior of prostate cancer. Notably, we found increasing SEPT6 expression might reverse the biological activity induced by miR-223-3p, which might be a potential therapeutic target for PCa.
微小RNA(miRNA)在包括前列腺癌、膀胱癌和肾癌在内的泌尿系统癌症中经常呈现表达改变。近期研究报道了miR-223在癌症及其他疾病中的表达改变。在系统性红斑狼疮和类风湿关节炎中,miR-223表达上调。在肿瘤性疾病中,与正常组织相比,miR-223在胰腺癌、胃癌等的血浆或血清以及癌组织中被证实呈高表达。然而,miR-223的表达改变是否与前列腺癌(PCa)相关及其在PCa中的潜在功能仍不明确。在本研究中,我们首先发现miR-223-3p在前列腺癌组织中上调,然后我们使用DU145、PC3和LNCaP细胞系研究miR-223-3p在PCa中的功能作用。我们的数据表明,miR-223-3p可能靶向SEPT6基因并促进前列腺癌的生物学行为。值得注意的是,我们发现增加SEPT6的表达可能会逆转miR-223-3p诱导的生物学活性,这可能是PCa的一个潜在治疗靶点。