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Diosgenin affect human gastric cancer BGC-823 and SGC-7901 cells through MAPK pathways |
WU Yuan-yuan1, CUI Guo-xing1, MA Tie-liang2, DING Wei-liang2, GE Zhi-jun3, TANG Zhi-an4 |
(1.Department of Gastroenterology,2.Central Laboratory,3.Department of Critical Care Medicine,4.Department of Traditional Chinese Medicine,the Affiliated Yixing Hospital of Jiangsu University,Yixing Jiangsu 214200,China) |
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Abstract Objective: To discuss the role of diosgenin in the proliferation, invasion,migration and apoptosis of human gastric cancer BGC-823 and SGC-7901 cells via MAPK signaling pathways. Methods: Human gastric cancer cell lines BGC-823 and SGC-7901 were cultured in vitro and treated with diosgenin. Proliferation rate, cell migration and invasion were measured by MTT method via Transwell assay. And protein expression of apoptosis-associated protein (AAP) BAX, apoptosis inhibitor protein Bcl-2 and Erk1/2,JNK and p38 proteins of MAPK pathways were measured by Western Blot. Results: When BGC-823 and SGC-7901 cells were treated with diosgenin,the proliferation, migration and invasion of BGC-823 and SGC-7901 cells were significantly decreased. The apoptosis of both cells was enhanced to a certain extent. As to the correlation of gastric cancer cells and MAPK pathways,we found that p-p38 protein expression level after diosgenin treated was dramatically down-regulated; however,the expression levels of Erk1/2,JNK,p38,p-Erk1/2 and p-JNK were negligible. Conclusion: Diosgenin might affect the proliferation,invasion,migration and apoptosis of human gastric cancer BGC-823 and SGC-7901 cells through p-p38 of MAPK pathways.
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[1] |
. [J]. Journal of Jiangsu University(Medicine Edition), 2018, 28(05): 454-458. |
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