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Supplementary Figure S6 from Alpha-Smooth Muscle Actin (ACTA2) Is Required for Metastatic Potential of Human Lung Adenocarcinoma

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posted on 2023-03-31, 17:20 authored by Hye Won Lee, Young Mi Park, Se Jeong Lee, Hyun Jung Cho, Duk-Hwan Kim, Jung-Il Lee, Myung-Soo Kang, Ho Jun Seol, Young Mog Shim, Do-Hyun Nam, Hyeon Ho Kim, Kyeung Min Joo

Supplementary Figure S6 - PDF file 30K, Supplementary Figure S6. Silencing of FAK and c-MET by specific siRNAs in PC14PE6 (A) and H322 (B) cells To investigate whether ACTA2 silencing inhibited migratory and invasive activity by suppressing FAK and c-MET expression, silencing of FAK and c-MET using specific siRNA was checked. PC14PE6 and H322 cells were transfected with each siRNA using Lipofectamine2000; 48 hours post-transfection, whole cell lysates were prepared and the level of FAK and c-MET was determined by Western blot

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ARTICLE ABSTRACT

Purpose: Metastatic relapse of primary lung cancer leads to therapeutic resistance and unfavorable clinical prognosis; therefore, identification of key molecules associated with metastatic conversion has significant clinical implications. We previously identified a link between early brain metastasis of lung adenocarcinoma and amplification of the α-smooth muscle actin (ACTA2) gene. The aim of present study was to investigate the prognostic and functional significance of ACTA2 expression in cancer cells for the metastatic potential of lung adenocarcinomas.Experimental Design:ACTA2 expression was analyzed in tumor cells from 263 patients with primary lung adenocarcinomas by immunohistochemistry, and was correlated with clinicopathologic parameters. The expression of ACTA2 in human lung adenocarcinoma cells was modulated with short hairpin RNAs (shRNA) and siRNAs specifically targeting ACTA2.Results: The patients with lung adenocarcinomas with high ACTA2 expression in tumor cells showed significantly enhanced distant metastasis and unfavorable prognosis. ACTA2 downregulation remarkably impaired in vitro migration, invasion, clonogenicity, and transendothelial penetration of lung adenocarcinoma cells without affecting proliferation. Consistent with the in vitro results, depletion of ACTA2 in human lung adenocarcinoma PC14PE6 cells significantly reduced their metastatic potential without altering their tumorigenic potential. Expression of c-MET and FAK in lung adenocarcinoma cells was also reduced by ACTA2-targeting siRNAs and shRNAs, and was accompanied by a loss of mesenchymal characteristics.Conclusions: These findings indicate that ACTA2 regulates c-MET and FAK expression in lung adenocarcinoma cells, which positively and selectively influence metastatic potential. Therefore, ACTA2 could be a promising prognostic biomarker and/or therapeutic target for metastatic lung adenocarcinoma. Clin Cancer Res; 19(21); 5879–89. ©2013 AACR.

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