Аннексин A8 регулирует пролиферацию клеток немелкоклеточного рака легкого человека линии A549 за счет регуляции сигнального пути EGFR-Akt-mTOR

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]
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.

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