In vivo and in vitro effects of hyperplasia suppressor gene on the proliferation and apoptosis of lung adenocarcinoma A549 cells
العنوان: | In vivo and in vitro effects of hyperplasia suppressor gene on the proliferation and apoptosis of lung adenocarcinoma A549 cells |
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المؤلفون: | Zhen-Qing Sun, Zhou Wang, Gang Chen, Hefei Li, Qiang Guo |
المصدر: | Bioscience Reports. 38 |
بيانات النشر: | Portland Press Ltd., 2018. |
سنة النشر: | 2018 |
مصطلحات موضوعية: | 0301 basic medicine, A549 cell, medicine.diagnostic_test, Chemistry, Cell growth, Biophysics, Cell Biology, Cell cycle, medicine.disease, Biochemistry, Flow cytometry, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, medicine.anatomical_structure, Apoptosis, 030220 oncology & carcinogenesis, medicine, Cancer research, Adenocarcinoma, Gene silencing, Molecular Biology, B cell |
الوصف: | Lung adenocarcinoma is the most common subtype of non-small cell lung cancer (NSCLC). Hyperplasia suppressor gene (HSG) has been reported to inhibit cell proliferation, migration, and remodeling in cardiovascular diseases. However, there lacks systematic researches on the effect of HSG on the apoptosis and proliferation of lung adenocarcinoma A549 cells and data of in vivo experiments. The present study aims to investigate the effects of HSG gene silencing on proliferation and apoptosis of lung adenocarcinoma A549 cells. The human lung adenocarcinoma A549 cell was selected to construct adenovirus vector. Reverse transcription-quantitative PCR (RT-qPCR) and Western blot analysis were conducted to detect expressions of HSG and apoptosis related-proteins. Cell Counting Kit (CCK)-8 assay was performed to assess A549 cell proliferation and flow cytometry to analyze cell cycle and apoptosis rate. The BALB/C nude mice were collected to establish xenograft model. Silenced HSG showed decreased mRNA and protein expressions of HSG, and elevated A549 cell survival rates at the time point of 24, 48, and 72 h. The ratio of cells at G0/G1 phase and apoptosis rate decreased and the ratio of cells at S- and G2/M phases increased following the silencing of HSG. There were decreases of B cell lymphoma-2 (Bcl-2)-associated X protein (Bax), Caspase-3, and Caspase-8 expressions but increases in Bcl-2 induced by silenced HSG. As for the xenograft in nude mice, tumor volume increased, and apoptosis index (AI) decreased after HSG silencing. These results indicate that HSG gene silencing may promote the proliferation of A549 cells and inhibit the apoptosis. HSG may be a promising target for the treatment of lung adenocarcinoma. |
تدمد: | 1573-4935 0144-8463 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::6efe1a858d90d6b404b090f263be9cda https://doi.org/10.1042/bsr20180391 |
حقوق: | OPEN |
رقم الأكسشن: | edsair.doi...........6efe1a858d90d6b404b090f263be9cda |
قاعدة البيانات: | OpenAIRE |
تدمد: | 15734935 01448463 |
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