Lin Tao, Zhou Shiming, Gao Hui, Li Yuqiao, Sun Lijiang
1 Department of Urology, The Affiliated Hospital of Qingdao University, Qingdao, China.
2 Department of Urology, Liaocheng People's Hospital, Liaocheng, China.
Technol Cancer Res Treat. 2018 Jan 1;17:1533033818790536. doi: 10.1177/1533033818790536.
We evaluated whether human microRNA-325 may be a potential biomarker and tumor regulator in bladder cancer.
Human microRNA-325 expression was probed by quantitative real-time polymerase chain reaction in both in vitro bladder cancer cell lines and in vivo bladder carcinoma tissues retrieved from patients with cancer. The prognostic potential of human microRNA-325 in predicting postoperative overall survival of patients with bladder cancer was estimated. Endogenous human microRNA-325 was overexpressed by lentiviral transduction in bladder cancer cell lines, T24 and 5637 cells. The tumor regulatory effects of human microRNA-325 upregulation on T24 and 5637 cells were evaluated both in vitro and in vivo.
Human microRNA-325 was aberrantly downregulated in both bladder cell lines and human bladder carcinomas. Lowly expressed human microRNA-325 in bladder carcinoma was closely associated with poor postoperative overall survival of patients with cancer. In T24 and 5637 cells, virally transduced cells had markedly upregulated human microRNA-325 expressions. Biochemical assays demonstrated that human microRNA-325 upregulation in bladder cancer had tumor-suppressive functions by decreasing cancer proliferation, cisplatin chemoresistance, and cancer migration in vitro and hindering transplantation growth in vivo and cell cycle transition.
Human microRNA-325 is lowly expressed and may serve as a potential prognostic biomarker in human bladder cancer. After further validation, human microRNA-325 may be a novel therapeutic target for suppressing carcinoma in patients with bladder cancer.
我们评估了人类微小RNA - 325是否可能是膀胱癌的潜在生物标志物和肿瘤调节因子。
通过定量实时聚合酶链反应检测体外膀胱癌细胞系以及从癌症患者体内获取的膀胱癌组织中人类微小RNA - 325的表达。评估人类微小RNA - 325对膀胱癌患者术后总生存期的预后潜力。通过慢病毒转导在膀胱癌细胞系T24和5637细胞中过表达内源性人类微小RNA - 325。在体外和体内评估人类微小RNA - 325上调对T24和5637细胞的肿瘤调节作用。
人类微小RNA - 325在膀胱癌细胞系和人类膀胱癌中均异常下调。膀胱癌中低表达的人类微小RNA - 325与癌症患者术后较差的总生存期密切相关。在T24和5637细胞中,病毒转导的细胞中人类微小RNA - 325表达明显上调。生化分析表明,膀胱癌中人类微小RNA - 325的上调具有肿瘤抑制功能,可通过降低体外癌细胞增殖、顺铂化疗耐药性和癌细胞迁移,以及阻碍体内移植瘤生长和细胞周期转变来实现。
人类微小RNA - 325低表达,可能作为人类膀胱癌的潜在预后生物标志物。经过进一步验证后,人类微小RNA - 325可能成为抑制膀胱癌患者肿瘤的新型治疗靶点。