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miR-425-5p检测的临床价值及其与胃癌细胞增殖和凋亡的关系

Clinical value of miR-425-5p detection and its association with cell proliferation and apoptosis of gastric cancer.

作者信息

Zhang Zhuoqi, Wen Ming, Guo Jian, Shi Jianwei, Wang Zhiyu, Tan Bibo, Zhang Gang, Zheng Xiangkui, Zhang Aimin

机构信息

Department of Gastrointestinal Surgery, Affiliated Hospital of Hebei University, Baoding, 071000, China.

Department of Gastrointestinal Surgery, Affiliated Hospital of Hebei University, Baoding, 071000, China.

出版信息

Pathol Res Pract. 2017 Aug;213(8):929-937. doi: 10.1016/j.prp.2017.05.009. Epub 2017 May 31.

Abstract

Researches have shown that miR-425-5p expression altered in lung, esophageal, and glial cancer. Similarly, in our previous study, we found miR-425-5p expression was up-regulated in GC cells and could promote gastric cancer (GC) cell invasion and metastasis. However, the functional mechanism and the prognostic significance of miR-425-5p in GC remain unclear. Therefore, the present study examined miR-425-5p expression in GC tissues and also evaluated miR-425-5p of the therapeutic and prognostic value. Moreover, with interference of miR-425-5p expression in cell lines, we investigated the molecular mechanism of miR-425-5p and the expression level was higher in GC tissues comparing with that in gastric tumor-adjacent mucosa. These results suggested that miR-425-5p over-expression may be associated with depth of invasion and TNM stages and can be a prognostic marker of poor outcome. After inhibition of miR-425-5p expression in MKN45 cells, the cell activity was weakened. The number of G0/G1 cells increased while G2/M and S cells decreased, and the cell apoptotic rates elevated (P<0.05). Some proliferation and apoptosis related genes were altered (P<0.05). Consequently, miR-425-5p can be considered as a marker of poor prognosis and it is probably involved in GC cell proliferation and apoptosis by regulating some of the genes which participate these processes.

摘要

研究表明,miR-425-5p在肺癌、食管癌和神经胶质瘤中表达发生改变。同样,在我们之前的研究中,我们发现miR-425-5p在胃癌细胞中表达上调,并且能够促进胃癌(GC)细胞的侵袭和转移。然而,miR-425-5p在胃癌中的功能机制和预后意义仍不清楚。因此,本研究检测了miR-425-5p在胃癌组织中的表达,并评估了miR-425-5p的治疗和预后价值。此外,通过干扰细胞系中miR-425-5p的表达,我们研究了miR-425-5p的分子机制,且与胃肿瘤旁黏膜相比,miR-425-5p在胃癌组织中的表达水平更高。这些结果表明,miR-425-5p的过表达可能与侵袭深度和TNM分期相关,并且可能是预后不良的一个标志物。在MKN45细胞中抑制miR-425-5p的表达后,细胞活性减弱。G0/G1期细胞数量增加,而G2/M期和S期细胞数量减少,细胞凋亡率升高(P<0.05)。一些增殖和凋亡相关基因发生改变(P<0.05)。因此,miR-425-5p可被视为预后不良的标志物,并且它可能通过调控一些参与这些过程的基因来参与胃癌细胞的增殖和凋亡。

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