癌症研究
生物
肝癌
癌症
癌细胞
细胞生长
基因敲除
小RNA
转染
细胞凋亡
小干扰RNA
活力测定
细胞
细胞迁移
细胞培养
庆大霉素保护试验
分子生物学
转移
基因
生物化学
遗传学
肝细胞癌
作者
Jun Huang,QINGYUAN XI,JIE XIONG,HAO PENG,Haitao Yang,Yu Sun,Robert M. Hoffman
出处
期刊:Anticancer Research
[International Institute of Anticancer Research (IIAR) Conferences 1997. Athens, Greece. Abstracts]
日期:2022-10-01
卷期号:42 (10): 4715-4725
标识
DOI:10.21873/anticanres.15976
摘要
Liver cancer is the third-most lethal cancer worldwide. Abnormal expression of microRNAs (miRNAs) modulates gene expression to exert oncogenic or tumor-suppressive effects in liver cancer. However, the biological role of miR-1303 in the progression of liver cancer and its regulatory mechanism has not been elucidated.The expression levels of miR-1303 were measured in liver-cancer tissues of patients and cell lines by RT-qPCR. Huh-7 and HepG2 liver-cancer cells were co-transfected by TLN1 and miR-1303 constructs. Cell viability was measured by the CCk-8 assay and colony-formation assay. Flow cytometry was used to measure cell apoptosis. Cell migration and invasion were determined by wound-healing and transwell-chamber assays. RT-PCR and western-blotting were used to determine miR-1303 inhibitor-associated marker expression, such as Bax, cleaved-caspase-3 and cleaved-caspase-9.miR-1303 expression was strongly up-regulated in liver-cancer tissues and cells. Knockdown of miR-1303 attenuated cell proliferation, migration and invasion, and induced apoptosis in liver-cancer cells. Talin 1 (TLN1) and miR-1303 expression were negatively correlated, possibly by miR-1303 targeting the TLN1 gene. TLN1 expression enhanced the efficacy of an miR-1303 inhibitor to reduce liver-cancer cell proliferation and invasion.miR-1303 plays an important role in liver cancer, which is inhibited by TLN1 expression.
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