Curcuma wenyujin Y. H. Chen et C. Ling n-Butyl Alcohol Extract Inhibits AGS Cell Helicobacter pyloriCagA+VacA+ Promoted Invasiveness by Down-Regulating Caudal Type Homeobox Transcription Factor and Claudin-2 Expression

作     者：JIN Hai-feng DAI Jin-feng MENG Li-na LU Bin JIN Hai-feng;DAI Jin-feng;MENG Li-na;LU Bin

作者机构：Department of Gastrointerology the First Affiliated Hospital of Zhejiang Chinese Medical University 

出 版 物：《Chinese Journal of Integrative Medicine》 (中国结合医学杂志（英文版）)

年 卷 期：2020年第26卷第2期

页      面：122-129页

核心收录：

学科分类：1007[医学-药学(可授医学、理学学位)] 1006[医学-中西医结合] 1005[医学-中医学] 1002[医学-临床医学] 10[医学] 100602[医学-中西医结合临床] 

基　　金：Supported by the National Natural Science Foundation of China(No.81202822) Fund of Zhejiang Province Administration of Traditional Chinese Medicine,China(No.2016ZA092/2017ZKL008) Key Laboratory of Pathology and Physiology of Digestive Tract Diseases in Zhejiang Province,China 

主　　题：Helicobacter pylori gastric cancer AGS zinefinger ebox binding homeobox 1 caudal type homeobox transcription factor claudin・2 Chinese medicine 

摘      要：Objective:To investigate the effects and possible mechanisms of action of Curcuma wenyujin Y.H.Chen et C.Ling n-Butyl alcohol extract(CWNAE)on repression of human gastric cancer(GC)AGS cell invasion induced by co-culturing with Helicobacter pylori(HP).Methods:AGS cells were cultured with HP of positive or negative cytotoxin-associated gene A(Cag A)and vacuolating cytotoxin gene A(Vac A)expression(Cag A+/-or Vac A+/-)and divided into 5 group.Group A was cultured without HP as a control,Group B with HPCagA+VacA+,Group C with HPCagA-VacA-,Group D with HPCagA+VacA+and CWNAE,and Group E with HPCag A-Vac Aand CWNAE.Methylthiazolyldiphenyl-tetrazolium bromide(MTT)and tumor invasion assays,examinations of morphology and ultramicroscopic structures,quantitative real-time polymerase chain reaction and Western blots were performed to measure the effects and uncover the mechanisms behind these effects of HPCagA+VacA+and CWNAE on the epithelial-mesenchymal transition(EMT)of AGS cells.Results:The 10%inhibitory concentration of CWNAE against AGS cells after a 48 h incubation was 19.73±1.30μg/m L.More AGS cells were elongated after co-culturing with HPCagA+VacA+than after culturing with HPCagA-VacA-.In tumor invasion assays,HPCagA+VacA+significantly enhanced the invasiveness of AGS cells compared to the other experimental groups(all P value0.05),and this effect was inhibited by CWNAE.Treatment with CWNAE normalized tight junctions and reduced the number of pseudopodia of AGS cells co-cultured with HPCagA+VacA+.HPCagA+VacA+up-regulated zincfinger ebox binding homeobox 1(ZEB1)in AGS cells after co-culturing for 24 h.Expression of caudal type homeobox transcription factor(CDX-2)and claudin-2 was significantly increased by HPCagA+VacA+(P0.05),but not by HPCagA-VacA-.Conclusions:HPCagA+VacA+promoted the invasiveness of AGS cells through up-regulation of ZEB1 transcription and claudin-2 and CDX-2 expression.CWNAE inhibited these effects of HPCagA+VacA+on AGS cells by down-regulating ZEB1 transcription,and CDX-2 and claudin-2 expression.