Influence of oridonin on EC9706 cell proliferation and apoptosis
Liu Junba
Abstract
Liu Junba
Abstract
Aim:To study the influence of oridonin on esophageal squamous cell carcinoma EC9706 cell proliferation and apoptosis in vitro. Methods:MTT assay was used to detect the inhibition effect of oridonin on the growth of EC9706; flow cytometry was applied to detect the impact of oridonin on cell cycle and apoptosis of EC9706,and calculated the apoptosis rate of cells; change of Ca2 +fluorescence intensity of EC9706 affected by different concentrations of oridonin was observed by laser scanning confocal microscope. Results:MTT assay showed that the inhibition rate in the experiment group increased with the rising of concentration( F = 370. 600,P 0. 001) after oridonin acting on EC9706; results of cell cycle detected by flow cytometry showed that the number of cell in G 0 and G 1 stage increased notably after oridonin acting on EC9706 for 48 hour respectively( F = 24. 200,P 0. 001); results of apoptosis showed that oridonin could obviously inducethe apoptosis of EC9706( P 0. 05),and the effect was the best when the oridonin concentration was 40 μmol/L( F = 10. 214,37. 820,P 0. 001). Different concentrations of oridonin could increase Ca2 +fluorescence intensity of EC9706, and the difference was significant( F = 24. 400,P 0. 001). Conclusion:oridonin can improve the inhibition effects on proliferation and apoptosis of EC9706 cell.
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.
Aim:To study the influence of oridonin on esophageal squamous cell carcinoma EC9706 cell proliferation and apoptosis in vitro. Methods:MTT assay was used to detect the inhibition effect of oridonin on the growth of EC9706; flow cytometry was applied to detect the impact of oridonin on cell cycle and apoptosis of EC9706,and calculated the apoptosis rate of cells; change of Ca2 +fluorescence intensity of EC9706 affected by different concentrations of oridonin was observed by laser scanning confocal microscope. Results:MTT assay showed that the inhibition rate in the experiment group increased with the rising of concentration( F = 370. 600,P 0. 001) after oridonin acting on EC9706; results of cell cycle detected by flow cytometry showed that the number of cell in G 0 and G 1 stage increased notably after oridonin acting on EC9706 for 48 hour respectively( F = 24. 200,P 0. 001); results of apoptosis showed that oridonin could obviously inducethe apoptosis of EC9706( P 0. 05),and the effect was the best when the oridonin concentration was 40 μmol/L( F = 10. 214,37. 820,P 0. 001). Different concentrations of oridonin could increase Ca2 +fluorescence intensity of EC9706, and the difference was significant( F = 24. 400,P 0. 001). Conclusion:oridonin can improve the inhibition effects on proliferation and apoptosis of EC9706 cell.
Key concepts: Apoptosis, Flow cytometry, Cell growth, MTT assay, Cell cycle, Molecular biology, Chemistry, Cell