Mechanism of sinomenine in regulating M2 macrophage polarization induced by gastric cancer cells

Yifei Chen; Mudan Ren; Xinlan LU; Guifang LU; Dan Zhang; Yan Zhao; Yarui LI; Dan Guo; Shuixiang HE

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Mechanism of sinomenine in regulating M2 macrophage polarization induced by gastric cancer cells

VernacularTitle:青藤碱调节胃癌细胞诱发的巨噬细胞M2极化的机制
Author: Yifei CHEN ¹ ; Mudan REN ¹ ; Xinlan LU ¹ ; Guifang LU ¹ ; Dan ZHANG ¹ ; Yan ZHAO ¹ ; Yarui LI ¹ ; Dan GUO ¹ ; Shuixiang HE ¹
Author Information

1. Department of Gastroenterology, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an 710061, China
Publication Type:Journal Article
Keywords: sinomenine; gastric cancer; M2 macrophage polarization; STAT6; IL-6
From: Journal of Xi'an Jiaotong University(Medical Sciences) 2022;43(3):436-443
CountryChina
Language:Chinese
Abstract: 【Objective】 To study the role and mechanism of sinomenine in the macrophage polarization induced by gastric cancer cells. 【Methods】 Sinomenine was added to gastric cancer cells BGC-823 and MKN-45， cell viability was measured by CCK-8， cell proliferation was measured by colony formation experiment， Co-culture and Transwell cell migration experiments were used to evaluate the recruitment and polarization of macrophages by sinomenine， flow cytometry was used to evaluate the polarization of macrophages， and qRT-PCR and Western blot were used to detect the expression of gene RNA and protein levels. 【Results】 Sinomenine could inhibit the proliferation of gastric cancer cells and the recruitment of gastric cancer cells to macrophages， thus promoting macrophage M2 polarization. It simultaneously inhibited the expression of STAT6 as well as the expression and phosphorylation of C/EBPβ. When STAT6 is overexpressed， it could reduce these inhibitory effects of sinomenine on gastric cancer cells. Further research found that STAT6 mediated the secretion of IL-6 by gastric cancer cells， which was the cause of sinomenine-mediated macrophage recruitment and M2 polarization. 【Conclusion】 The natural drug sinomenine has a good tumor-suppressing ability against gastric cancer， directly inhibits the survival and migration of gastric cancer cells， and inhibits the expression of IL-6 and the M2 phenotype in the tumor microenvironment， reshapes the tumor environment， and reduces the risk of M2 type macrophages for gastric cancer tumors.