A549电池
PI3K/AKT/mTOR通路
癌症研究
蛋白激酶B
转染
基因敲除
细胞生物学
细胞生长
小干扰RNA
生物
细胞培养
化学
信号转导
分子生物学
遗传学
作者
G. J. Zhou,Yuhan Sun,Yuankai Shi,Qiming Zhang,Lei Zhang,Liying Cui,G. X. Sun
出处
期刊:Molekulârnaâ biologiâ
[Pleiades Publishing]
日期:2021-01-01
标识
DOI:10.31857/s0026898421050116
摘要
Annexin A8 (ANXA8) is a member of the annexin family, which had been reported to regulate multiple cancer cellular processes including proliferation, metastasis and inflammation. However, the specific role of ANXA8 in lung cancer cell biology remains unknown. Our previous transcriptome study revealed that ANXA8 mRNA was downregulated in curcumin analog (MHMD) -treated human non-small lung cancer cells (A549 cell line). Here, we continued to study the ANXA8 expression in A549 cells using reverse transcription-quantitative PCR and Western blotting, compared with that in human normal bronchial epithelium cells (BE-AS-2B cell line). Overexpression of ANXA8 via transfection of pEGFP-ANXA8 recombinant vector contributed to the proliferation and migration of A549 cells. Moreover, the cell cycle protein cyclin E1 was upregulated in ANXA8-transfected A549 cells. Knockdown of ANXA8 using an RNA interference technique decreased A549 cell viability and restrained their migration in vitro. The expression levels of multiple cellular factors, including EGFR, PI3K, Akt, mTOR, p70S6K and 4EBP1, in the epidermal growth factor receptor (EGFR) signaling pathway were also altered by ANXA8 knockdown or overexpression in A549 cells, which confirmed the activation of the EGFR/Akt/mTOR signaling pathway by ANXA8. The present results provided evidence to support further investigation of the functional identification of ANXA8 in lung cancer cells in the future.
科研通智能强力驱动
Strongly Powered by AbleSci AI