Effect of A1a-Gln on Fas Ligand gene expression and apoptosis of lymphocyte induced by human colon carcinoma cell.
Bao Guoqiang
Abstract
Bao Guoqiang
Abstract
Objective To study the effect of A1a-Gln on Fas Ligand mRNA expression and apoptosis of lymphocyte induced by human colon cancer cells line SW480 with cell culture. Methods Different concentrations of Ala-Gln were added in the cultured human colon cancer cells line SW480.The changes of Fas Ligand mRNA was detected by the reverse transcription polymerase chain reaction method(RT-PCR)and apoptosis rate of lymphocyte induced by SW480 cell was measured by flow cytometry analysis. Results RT-PCR revealed that the higher concentration A1a-Gln down-regulated Fas Ligand mRNA expression on SW480 cell(P0.05); flow cytometry showed that the higher concentration Ala-Gln reduced apoptosis rate of lymphocyte induced by SW480 cell(P0.05). The comparisons with different concentrations teams of Ala-Gln have statistical significance(P0.05). Conclusion Ala-Gln in certain concentration can down-regulated Fas Ligand mRNA expression of human colon cancer cells line SW480. For the same time, the down-regulative effect can inhibit SW480 cells to counterattack lymphocyte.
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 study the effect of A1a-Gln on Fas Ligand mRNA expression and apoptosis of lymphocyte induced by human colon cancer cells line SW480 with cell culture. Methods Different concentrations of Ala-Gln were added in the cultured human colon cancer cells line SW480.The changes of Fas Ligand mRNA was detected by the reverse transcription polymerase chain reaction method(RT-PCR)and apoptosis rate of lymphocyte induced by SW480 cell was measured by flow cytometry analysis. Results RT-PCR revealed that the higher concentration A1a-Gln down-regulated Fas Ligand mRNA expression on SW480 cell(P0.05); flow cytometry showed that the higher concentration Ala-Gln reduced apoptosis rate of lymphocyte induced by SW480 cell(P0.05). The comparisons with different concentrations teams of Ala-Gln have statistical significance(P0.05). Conclusion Ala-Gln in certain concentration can down-regulated Fas Ligand mRNA expression of human colon cancer cells line SW480. For the same time, the down-regulative effect can inhibit SW480 cells to counterattack lymphocyte.
Key concepts: Apoptosis, Flow cytometry, Fas ligand, Lymphocyte, Molecular biology, Cell culture, Colorectal cancer, Messenger RNA