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

上皮-间质转换 癌症研究 丹参 胃粘膜 癌症 炎症 细胞凋亡 车站3 化学 一氧化氮 细胞迁移 药理学 细胞 医学 病理 免疫学 内科学 转移 生物化学 中医药 替代医学
作者
Dan Liang,Shiyun Tang,Lu Liu,Maoyuan Zhao,Xiao Ma,Yanling Zhao,Caifei Shen,Qingsong Liu,Jianyuan Tang,Jinhao Zeng,Nianzhi Chen
出处
期刊:International Immunopharmacology [Elsevier BV]
卷期号:124: 110902-110902 被引量:8
标识
DOI:10.1016/j.intimp.2023.110902
摘要

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.To investigate the effect and mechanism of Tan-I in intervening GPLs, and provide a new therapeutic strategy for prevention of GC.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.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, TNFα and IL-1β. Tan-I reversed the EMT and inflammatory processes by regulating p38 and STAT3.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.
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