Enhancement of Cytotoxicity of Fluorouracil by Rosiglitazone in Colon Cancer
Sun Li
Abstract
Sun Li
Abstract
Objective To investigate the enhancenment of cytotoxicity of fluorouracil on human colon cancer by rosiglitazone. Methods Human colon cancer (HT-29) cells were cultured in vitro. HT-29 cell line was treated with various concentrations of Rosiglitazone or 5-Fu or both, cell proliferation was evaluated by MTT assay, Trypan blue exclusion method was used to test the influence of growth curve in HT-29 cells. The apoptosis of HT-29 cells was determined by PI staining flow cytometry and cell cycle was analyzed by using flow cytometry. Results Rosiglitazone significantly increased proliferation and growth inhibitoty effect of 5-Fu to HT-29 cells at 1.5μmol/L. PI staining flow cytometry data showed the apoptosis of HT-29 cells was induced and cell cycle was arrested at G1 stage by rosiglitazone;rosiglitazone (1.0μmol/L) significantly promoted apoptosis inducation of HT-29 cells by 5-Fu. Conclusions Rosiglitazone can enhance growth inhibition and apoptosis inducation of 5-Fu on HT-29 cells. The effect of chemosenitization to 5-Fu of rosiglitazone are associated with apoptosis and cell cycle arrested at G1 stage of HT-29 cells.
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Objective To investigate the enhancenment of cytotoxicity of fluorouracil on human colon cancer by rosiglitazone. Methods Human colon cancer (HT-29) cells were cultured in vitro. HT-29 cell line was treated with various concentrations of Rosiglitazone or 5-Fu or both, cell proliferation was evaluated by MTT assay, Trypan blue exclusion method was used to test the influence of growth curve in HT-29 cells. The apoptosis of HT-29 cells was determined by PI staining flow cytometry and cell cycle was analyzed by using flow cytometry. Results Rosiglitazone significantly increased proliferation and growth inhibitoty effect of 5-Fu to HT-29 cells at 1.5μmol/L. PI staining flow cytometry data showed the apoptosis of HT-29 cells was induced and cell cycle was arrested at G1 stage by rosiglitazone;rosiglitazone (1.0μmol/L) significantly promoted apoptosis inducation of HT-29 cells by 5-Fu. Conclusions Rosiglitazone can enhance growth inhibition and apoptosis inducation of 5-Fu on HT-29 cells. The effect of chemosenitization to 5-Fu of rosiglitazone are associated with apoptosis and cell cycle arrested at G1 stage of HT-29 cells.
Key concepts: Rosiglitazone, Apoptosis, Flow cytometry, Cell cycle, Medicine, Trypan blue, Cell growth, Cytotoxicity