细胞凋亡
细胞周期
小RNA
癌症研究
癌细胞
癌基因
细胞生长
癌症
基因敲除
生物
下调和上调
细胞生物学
蛋白激酶B
癌变
活力测定
分子生物学
细胞周期检查点
MAPK/ERK通路
分子医学
转染
基因沉默
基因
生物化学
遗传学
作者
Xinxin Li,Jinpeng Yuan,Qiangjian Cao,Aosi Xie,Juntian Chen
标识
DOI:10.3892/ijmm.2020.4603
摘要
The aberrant expression of microRNA (miRNAor miR)‑383‑5p has been found in numerous types of cancer. However, the function of miR‑383‑5p in gastric cancer (GC) remains elusive and requires further investigation. In the present study, the level of miR‑383‑5p and cancerous inhibitor of PP2A (CIP2A) in GC cell lines was determined by reverse transcription‑quantitative PCR analysis. GC cell proliferation, apoptosis and cell cycle distribution were determined by the MTT assay and flow cytometry, respectively. The mRNA target of miR‑383‑5p was identified by dual luciferase activity assay. It was observed that the expression of miR‑383‑5p was lower and that of CIP2A was higher in GC cells compared with the GES‑1 normal human gastric epithelial cell line. Transfectoin with miR‑383‑5p mimic significantly inhibited GC cell proliferation, while it promoted cell apoptosis and G0/G1 arrest by targeting CIP2A. Taken together, the findings of the present study demonstrate that miR‑383‑5p inhibits GC cell proliferation and promotes apoptosis and G0/G1 arrest by targeting CIP2A, indicating that targeting miR‑383‑5p may hold promise as a future therapeutic strategy for patients with GC.
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