Enhanced plasma miR-26a-5p promotes the progression of bladder cancer via targeting PTEN

被引:29
作者
Wang, Hui [1 ,2 ]
Hu, Zhao [1 ]
Chen, Li [3 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Nephrol, Jinan 250014, Shandong, Peoples R China
[2] Fourth Hosp Jinan City, Dept Nephrol, Jinan 250031, Shandong, Peoples R China
[3] Shandong Univ, Qilu Hosp, Dept Endocrinol, 44 Wenhua Xi Rd, Jinan 250014, Shandong, Peoples R China
关键词
miR-26a-5p; bladder cancer; PTEN; biomarker; URINE BASED TESTS; MIRNA SIGNATURE; PROLIFERATION; MIGRATION; INVASION; CELLS; IDENTIFICATION; ACTIVATION;
D O I
10.3892/ol.2018.9163
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The current study aimed to evaluate the expression and specific role of miR-26a-5p in the progression of bladder cancer (BC). Reverse transcription-quantitative polymerase chain reaction analysis was performed to evaluate the level of miR-26a-5p in BC cancer and healthy controls. The present data showed that plasma miR-26a-5p was significantly increased in BC patients. Furthermore, BC tissues exhibited greater levels of miR-26a-5p compared with adjacent non-neoplastic tissues-26a-5p. Compared with BC patients at Ta-T1 stage, the level of miR-26a-5p was significantly elevated in BC patients T2. BC patients at G3 stage demonstrated a higher plasma miR-26a-5p level compared with those at G1/2 stage. Receiver operating characteristic (ROC) analysis indicated that miR-26a-5p could differentiate BC patients from controls. Additionally, Kaplan-Meier analysis demonstrated that plasma miR-26a-5p negatively correlated with survival of BC patients. Dual luciferase reporter assay indicated that miR-26a-5p significantly suppressed the relative luciferase activity of pmirGLO-PTEN-3UTR compared with the control. In conclusion, the current study indicated novel data that the levels of plasma miR-26a-5p was significantly increased in BC patients. Furthermore, the present study suggested that determination of plasma miR-26a-5p level could help to distinguish BC patients from healthy controls via targeting PTEN.
引用
收藏
页码:4223 / 4228
页数:6
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