Tanshinone I attenuates gastric precancerous lesions by inhibiting epithelial mesenchymal transition through the p38/STAT3 pathway

被引:6
|
作者
Liang, Dan [1 ]
Tang, Shiyun [1 ]
Liu, Lu [2 ]
Zhao, Maoyuan [1 ]
Ma, Xiao [2 ]
Zhao, Yanling [3 ]
Shen, Caifei [4 ]
Liu, Qingsong [5 ]
Tang, Jianyuan [6 ]
Zeng, Jinhao [5 ]
Chen, Nianzhi [7 ]
机构
[1] Hosp Chengdu Univ Tradit Chinese Med, Chengdu, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Coll Pharm, Chengdu, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Pharm, Beijing, Peoples R China
[4] Hosp Chengdu Univ Tradit Chinese Med, Dept Endoscopy Ctr, Chengdu, Peoples R China
[5] Hosp Chengdu Univ Tradit Chinese Med, Dept Gastroenterol, Chengdu, Peoples R China
[6] Hosp Chengdu Univ Tradit Chinese Med, TCM Regulating Metab Dis Key Lab Sichuan Prov, Chengdu, Peoples R China
[7] Chongqing Med Univ, Coll Biomed Engn, State Key Lab Ultrasound Med & Engn, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
Gastric precancerous lesions; Epithelial-mesenchymal transition; Tanshinone I; p38/STAT3; Gastric cancer;
D O I
10.1016/j.intimp.2023.110902
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Gastric precancerous lesions (GPLs) are omens for gastric cancer (GC), which developing with a series of pathological changes of gastric mucosa. Reversing epithelial-mesenchymal transition (EMT) in gastric mucosa is the main approach to restrain GPLs from evolving into cancer. Tanshinone I (Tan-I), the active ingredients of traditional Chinese herb Salvia miltiorrhiza, has exhibited anticancer effect. Purpose: To investigate the effect and mechanism of Tan-I in intervening GPLs, and provide a new therapeutic strategy for prevention of GC. Methods: Gastric mucosal epithelial cells were treated with the N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) to construct MNNG-induced cell (MC cell) of gastric mucosa that undergoing EMT process. Then, this study explored the effect and mechanism of Tan-I in vitro. Subsequently, this study constructed GPL mice to clarify the exact efficacy and mechanism of Tan-I on GPLs. Results: Tan-I inhibited MC cell proliferation, invasion and migration. Simultaneously, the aberrant expression of E-cadherin and N-cadherin were reversed. Tan-I attenuated inflammation by reducing the release of nitric oxide, TNF alpha and IL-1 beta. Tan-I reversed the EMT and inflammatory processes by regulating p38 and STAT3. Conclusion: This study showed that Tan-I inhibited the progression of GPLs by reversing the EMT process and reducing inflammation by restraining the p38/STAT3 signaling pathway.
引用
收藏
页数:13
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