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논문 기본 정보

자료유형
학술저널
저자정보
Pan, Xue-Diao (College of Pharmacy, Guang dong Pharmaceutical University) Yang, Zhou-Ping (College of Pharmacy, Guang dong Pharmaceutical University) Tang, Qi-Ling (College of Pharmacy, Guang dong Pharmaceutical University) Peng, Tong (College of Pharmacy, Guang dong Pharmaceutical University) Zhang, Zheng-Bing (Pharmacy Department of Zhangzhou Health Vocational College) Zhou, Si-Gui (College of Pharmacy, Guang dong Pharmaceutical University) Wang, Gui-Xiang (College of Pharmacy, Guang dong Pharmaceutical University) He, Bing (College of Pharmacy, Guang dong Pharmaceutical University) Zang, Lin-Quan (College of Pharmacy, Guang dong Pharmaceutical University)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제15권 제20호
발행연도
2014.1
수록면
8,631 - 8,635 (5page)

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Glutathione S-transferase A1 (GSTA1) appears to be primarily involved in detoxification processes, but possible roles in lung cancer remain unclear. The objective of this study was to investigate the expression and function of GSTA1 in lung cancer cells. Real-time PCR and Western blotting were performed to assess expression in cancer cell lines and the normal lung cells, then verify the A549 cells line with stable overexpression. Localization of GSTA1 proteins was assessed by cytoimmunofluorescence. Three double-strand DNA oligoRNAs (SiRNAs) were synthesized prior to being transfected into A549 cells with Lipofectamine 2000, and then the most efficient SiRNA was selected. Expression of the GSTA1 gene in the transfected cells was determined by real-time PCR and Western blotting. The viability of the transfected cells were assessed by MTT. Results showed that the mRNA and protein expression of A549 cancer cells was higher than in MRC-5 normal cells. Cytoimmunofluorescence demonstrated GSTA1 localization in the cell cytoplasm and/or membranes. Transfection into A549 cells demonstrated that down-regulated expression could inhibit cell viability. Our data indicated that GSTA1 expression may be a target molecule in early diagnosis and treatment of lung cancer.

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