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微小RNA-7通过抑制雷帕霉素靶蛋白提高胃癌细胞对顺铂的敏感性。

miR-7 Increases Cisplatin Sensitivity of Gastric Cancer Cells Through Suppressing mTOR.

作者信息

Xu Ning, Lian Yan-Jun, Dai Xiang, Wang Yuan-Jie

机构信息

Department of Gastrointestinal Surgery, Taizhou People's Hospital, Taizhou, Jiangsu, China.

出版信息

Technol Cancer Res Treat. 2017 Dec;16(6):1022-1030. doi: 10.1177/1533034617717863. Epub 2017 Jul 11.

Abstract

MicroRNAs have been reported to play an important role in diverse biological processes and cancer progression. MicroRNA-7 has been observed to be downregulated in human gastric cancer tissues, but the function of microRNA-7 in gastric cancer has not been well investigated. In this study, we demonstrate that the expression of microRNA-7 was significantly downregulated in 30 pairs of human gastric cancer tissues compared to adjacent normal tissues. Enforced expression of microRNA-7 inhibited cell proliferation and migration abilities of gastric cancer cells, BGC823 and SGC7901. Furthermore, microRNA-7 targeted mTOR in gastric cancer cells. In human clinical specimens, mTOR was higher expressed in gastric cancer tissues compared with adjacent normal tissues. More interestingly, microRNA-7 also sensitizes gastric cancer cells to cisplatin (CDDP) by targeting mTOR. Collectively, our results demonstrate that microRNA-7 is a tumor suppressor microRNA and indicate its potential application for the treatment of human gastric cancer in future.

摘要

据报道,微小RNA在多种生物学过程和癌症进展中发挥重要作用。已观察到微小RNA-7在人胃癌组织中表达下调,但微小RNA-7在胃癌中的功能尚未得到充分研究。在本研究中,我们证明与相邻正常组织相比,微小RNA-7在30对人胃癌组织中的表达显著下调。过表达微小RNA-7可抑制胃癌细胞BGC823和SGC7901的细胞增殖和迁移能力。此外,微小RNA-7在胃癌细胞中靶向mTOR。在人类临床标本中,与相邻正常组织相比,mTOR在胃癌组织中高表达。更有趣的是,微小RNA-7还通过靶向mTOR使胃癌细胞对顺铂(CDDP)敏感。总的来说,我们的结果表明微小RNA-7是一种肿瘤抑制性微小RNA,并表明其在未来治疗人类胃癌中的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c465/5762063/10e2b6d29634/10.1177_1533034617717863-fig1.jpg

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