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微小RNA-494通过靶向c-Myc抑制上皮性卵巢癌生长。

MiR-494 Inhibits Epithelial Ovarian Cancer Growth by Targeting c-Myc.

作者信息

Yuan Jialing, Wang Kana, Xi Mingrong

机构信息

Department of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China (mainland).

出版信息

Med Sci Monit. 2016 Feb 24;22:617-24. doi: 10.12659/msm.897288.

Abstract

BACKGROUND Epithelial ovarian cancer (EOC) is the most lethal malignant gynecological cancer. MicroRNAs (miRNAs) play important roles in the pathogenesis of ovarian cancer. The role of miR-494 in EOC has not been fully investigated. MATERIAL AND METHODS MiR-494 levels in ovarian cancer tissues and cells were tested by qRT-PCR. Cells were transfected with miR-494 mimics or miR-494 ASO by Lipofectamine. Bioinformatics algorithms from TargetScanHuman were used to predict the target genes of miR-494. The c-Myc protein level was assayed by Western blot. The interaction between miR-494 and c-Myc was confirmed by dual luciferase assays. RESULTS MiR-494 showed low levels in EOC tissues and cells. Overexpression of miR-494 inhibited cell growth and migration of EOC cells and vice versa. c-Myc is the targeted gene of miR-494. CONCLUSIONS MiR-494 has an anti-tumor role in EOC via c-Myc.

摘要

背景

上皮性卵巢癌(EOC)是最致命的妇科恶性肿瘤。微小RNA(miRNA)在卵巢癌的发病机制中起重要作用。miR-494在EOC中的作用尚未得到充分研究。

材料与方法

采用qRT-PCR检测卵巢癌组织和细胞中miR-494的水平。通过脂质体转染miR-494模拟物或miR-494反义寡核苷酸(ASO)转染细胞。使用TargetScanHuman的生物信息学算法预测miR-494的靶基因。通过蛋白质免疫印迹法检测c-Myc蛋白水平。通过双荧光素酶报告基因检测法确认miR-494与c-Myc之间的相互作用。

结果

miR-494在EOC组织和细胞中呈低水平表达。miR-494的过表达抑制了EOC细胞的生长和迁移,反之亦然。c-Myc是miR-494的靶基因。

结论

miR-494通过c-Myc在EOC中发挥抗肿瘤作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7c8/4768945/38d74c4fdf98/medscimonit-22-617-g001.jpg

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