Suppr超能文献

微小RNA-122过表达在抑制人胆管癌细胞增殖、侵袭及促进其凋亡中的作用

The Roles of MicroRNA-122 Overexpression in Inhibiting Proliferation and Invasion and Stimulating Apoptosis of Human Cholangiocarcinoma Cells.

作者信息

Liu Ning, Jiang Fan, He Tian-Lin, Zhang Jun-Kuan, Zhao Juan, Wang Chun, Jiang Gui-Xing, Cao Li-Ping, Kang Peng-Cheng, Zhong Xiang-Yu, Lin Tian-Yu, Cui Yun-Fu

机构信息

Department of General Surgery, Hainan Provincial people's Hospital, Haikou 570311, P.R. China.

Department of Geratology, Hainan Provincial people's Hospital, Haikou 570311, P.R. China.

出版信息

Sci Rep. 2015 Dec 21;5:16566. doi: 10.1038/srep16566.

Abstract

Our study investigated whether microRNA-122 (miR-122) played important roles in the proliferation, invasion and apoptosis of human cholangiocarcinoma (CC) cells. QBC939 and RBE cells lines were chosen and divided into five groups: miR-122 mimic group, anti-miR-122 group, negative control (NC) group, mock group and blank group. MiR-122 expression was measured by qRT-PCR. Roles of miR-122 in cell proliferation, apoptosis and invasion were investigated using MTT assay, flow cytometer and Transwell invasion assay, respectively. MiR-122 expression was lower in CC tissues and QBC939 cell than that in normal bile duct tissues, HCCC-9810 and RBE cells. In both QBC939 and RBE cells lines, miR-122 expression was higher in miR-122 mimic group than that in NC group, mock group and blank group; opposite results were found in anti-miR-122 group. Cell proliferation and invasion were remarkably inhibited in miR-122 mimic group after 48 h/72 h transfection, while apoptotic cells numbers were much greater in miR-122 mimic group; the opposite results were obtained from anti-miR-122 group (all P < 0.05). MiR-122 expression was significantly weaker in CC tissues, and miR-122 overexpression might play pivotal roles in inhibiting proliferation, stimulating apoptosis and suppressing invasion of CC cells, suggesting a new target for CC diagnosis and treatment.

摘要

我们的研究调查了微小RNA-122(miR-122)是否在人胆管癌(CC)细胞的增殖、侵袭和凋亡中发挥重要作用。选用QBC939和RBE细胞系,并将其分为五组:miR-122模拟物组、抗miR-122组、阴性对照组(NC)、模拟组和空白组。通过qRT-PCR检测miR-122的表达。分别采用MTT法、流式细胞仪和Transwell侵袭试验研究miR-122在细胞增殖、凋亡和侵袭中的作用。CC组织和QBC939细胞中miR-122的表达低于正常胆管组织、HCCC-9810和RBE细胞。在QBC939和RBE细胞系中,miR-122模拟物组中miR-122的表达均高于NC组、模拟组和空白组;抗miR-122组则得到相反的结果。转染48小时/72小时后,miR-122模拟物组的细胞增殖和侵袭受到显著抑制,而miR-122模拟物组的凋亡细胞数量则多得多;抗miR-122组得到相反的结果(所有P<0.05)。CC组织中miR-122的表达明显较弱,miR-122的过表达可能在抑制CC细胞增殖、刺激凋亡和抑制侵袭中起关键作用,提示其可作为CC诊断和治疗的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e12b/4685305/f0658b6483e2/srep16566-f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验