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Microarray-based apoptosis gene screening technique in trichostatin A-induced drug-resisted lung cancer A549/CDDP cells / 解放军医学杂志
Article em Zh | WPRIM | ID: wpr-850076
Biblioteca responsável: WPRO
ABSTRACT
Objective: To detect the expression profile changes of apoptosis-related genes in trichostatin A (TSA)-induced drug-resisted lung cancer cells A549/CDDP by microarray, in order to screen the target genes in TSA treating cisplatin-resisted lung cancer. Methods: A549/CDDP cells were treated by TSA for 24 hours. Total RNA was extracted and reversely transcribed into cDNA. Gene expression levels were detected by the NimbleGen whole genome microarray. Differences of expression profiles between TSA-treated and control group were measured by NimbleScan 2.5 software and GO analysis. Apoptosis and proliferation related genes were screened from the expression changed genes. Results: Compared with the control group, 85 apoptosis-related genes were up-regulated and 43 growth or proliferation related genes were down-regulated in the TSA-treated group. GO analysis showed that the functions of these genes are mainly regulating apoptosis, cell resistance to chemical stimuli protein, as well as regulating cell growth, proliferation and the biological process of maintaining the cell biological quality. TSA-activated not only the mitochondrial apoptotic pathways, but also the death receptor related apoptosis pathway, and down-regulated the drug resistance related genes BAG3 and ABCC2. Conclusion: TSA may cause the expression changes of apoptotic and proliferation genes in A549/CDDP cells, these genes may play a role in TSA treating cisplatin-resisted lung cancer.
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Texto completo: 1 Índice: WPRIM Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: Zh Revista: Medical Journal of Chinese People's Liberation Army Ano de publicação: 2016 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: Zh Revista: Medical Journal of Chinese People's Liberation Army Ano de publicação: 2016 Tipo de documento: Article