Trichostatin A Increases Radiosensitivity of Non-small Cell Lung Cancer A549 Cells
Li Su
Abstract
Li Su
Abstract
Objective:To investigate the activity of trichostatin A(TSA),one of the HDIs,on radiosensitize human non-small cell lung cancer(NSCLC) cell line A549 cells in vitro.Methods:A549 cells were exposed toγ-irradiation with or without TSA pre-treatment. MTT assay was performed to detect cell viability.Apoptosis was analyzed with Annexin V-PI staining by flow cytometry.The pro-apoptotic protein Bax expression in cytoplasm and mitochondria was detected by western blot.The changes of mitochondrial membrane potential(MMP) were measured by flow cytometry.Results:The pre-treatment with TSA 0.5μM radiosensitized A549 cells toγ-irradiation(5Gy) significantly by decreasing cell viability.γ-irradiation or TSA alone only caused small amount of apoptotic cells,as indicated by Annexin V positive cells.However,TSA pre-treatment enhancedγ-irradiation-induced apoptosis significantly.In the combined treatment group,mitochondrial Bax expression was higher than that in the other groups,and which decreased MMP significantly compared withγ-irradiation(5Gy) or TSA alone.Conclusions:TSA has potential to act as radio-sensitizer in A549 cells through Bax activation and mitochondrial apoptotic pathway.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To investigate the activity of trichostatin A(TSA),one of the HDIs,on radiosensitize human non-small cell lung cancer(NSCLC) cell line A549 cells in vitro.Methods:A549 cells were exposed toγ-irradiation with or without TSA pre-treatment. MTT assay was performed to detect cell viability.Apoptosis was analyzed with Annexin V-PI staining by flow cytometry.The pro-apoptotic protein Bax expression in cytoplasm and mitochondria was detected by western blot.The changes of mitochondrial membrane potential(MMP) were measured by flow cytometry.Results:The pre-treatment with TSA 0.5μM radiosensitized A549 cells toγ-irradiation(5Gy) significantly by decreasing cell viability.γ-irradiation or TSA alone only caused small amount of apoptotic cells,as indicated by Annexin V positive cells.However,TSA pre-treatment enhancedγ-irradiation-induced apoptosis significantly.In the combined treatment group,mitochondrial Bax expression was higher than that in the other groups,and which decreased MMP significantly compared withγ-irradiation(5Gy) or TSA alone.Conclusions:TSA has potential to act as radio-sensitizer in A549 cells through Bax activation and mitochondrial apoptotic pathway.
Key concepts: A549 cell, Apoptosis, Viability assay, Trichostatin A, Radiosensitivity, Molecular biology, Flow cytometry, Annexin