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微小RNA-27a(miR-27a)中的rs11671784 G/A变异通过降低miR-27a并增加靶标RUNX-1的表达来降低膀胱癌的化疗敏感性。

rs11671784 G/A variation in miR-27a decreases chemo-sensitivity of bladder cancer by decreasing miR-27a and increasing the target RUNX-1 expression.

作者信息

Deng Ying, Bai Hansong, Hu Honglin

机构信息

Department of Oncology, Sichuan Provincial People's Hospital, School of Clinical Medicine of University of Electronic Science and Technology of China, Chengdu 610000, China.

Department of Oncology, Sichuan Provincial People's Hospital, School of Clinical Medicine of University of Electronic Science and Technology of China, Chengdu 610000, China; Graduate School, Zunyi Medical College, Zunyi 563000, China.

出版信息

Biochem Biophys Res Commun. 2015 Mar 6;458(2):321-7. doi: 10.1016/j.bbrc.2015.01.109. Epub 2015 Feb 3.

Abstract

Single nucleotide polymorphism (SNP) rs11671784 is in the loop of pre-miR-27a and the G/A variation can significantly decrease mature miR-27a expression. This study explored the role of miR-27a in chemo-sensitivity of bladder cancer and how rs11671784 G/A variation affects the sensitivity. Blood and tumor samples from 89 bladder cancer cases were analyzed. In-vitro study was performed to explore the mechanism of chemo-sensitivity and the downstream target of miR-27a by using bladder cancer cell lines. This study identified a causative relationship between rs11671784 G/A variation, lowered miR-27a expression, increased RUNX-1 expression and following weakened chemo-sensitivity. rs11671784 G allele has significantly stronger effect over A allele in promoting chemo-sensitivity in bladder cancer. miR-27a mediates chemotherapy at least partially through reducing P-gp expression and increasing apoptosis. In addition, RUNX-1 is a novel direct target of miR-27a, which is involved in its regulation of chemo-sensitivity in bladder cancer.

摘要

单核苷酸多态性(SNP)rs11671784位于前体miR - 27a的环中,G/A变异可显著降低成熟miR - 27a的表达。本研究探讨了miR - 27a在膀胱癌化疗敏感性中的作用以及rs11671784 G/A变异如何影响敏感性。分析了89例膀胱癌患者的血液和肿瘤样本。利用膀胱癌细胞系进行体外研究,以探讨化疗敏感性机制及miR - 27a的下游靶点。本研究确定了rs11671784 G/A变异、miR - 27a表达降低、RUNX - 1表达增加以及随后化疗敏感性减弱之间的因果关系。rs11671784的G等位基因在促进膀胱癌化疗敏感性方面对A等位基因具有显著更强的作用。miR - 27a至少部分通过降低P - gp表达和增加细胞凋亡来介导化疗。此外,RUNX - 1是miR - 27a的一个新的直接靶点,其参与miR - 27a对膀胱癌化疗敏感性的调控。

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