Article(id=1317125611609510845, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317125500041015883, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.02.035, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1791956816818, onlineDateStr=2026-10-14, pubDate=1770652800000, pubDateStr=2026-02-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1791956816818, onlineIssueDateStr=2026-10-14, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1791956816818, creator=13701087609, updateTime=1791956816818, updator=13701087609, issue=Issue{id=1317125500041015883, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='2', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1770652800000', pubDateStr='2026-02-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1791956790217, creator='13701087609', updateTime=1791958795145, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1317133909368877755, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317125500041015883, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1317133909373072060, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317125500041015883, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=206, endPage=210, ext={EN=ArticleExt(id=1317125611823420350, articleId=1317125611609510845, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Tectoridin Induces Apoptosis and Autophagy in Gastric Cancer Cells Through PI3K/Akt/mTOR Signaling Pathway, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective To investigate the effect of Tectoridin(Tec)on autophagy and apoptosis of human gastric cancer cell line HGC-27.
Methods The cell proliferation ability was detected by CCK-8 and clone formation assay,the cell apoptosis rate was detected by flow cytometry,and the autophagy inhibitor 3-MA was used to detect the autophagy. Western blotting was used to detect the protein expression levels of Beclin-1,Bcl-2,Bax and p53. Bioinformatics methods were used to predict the potential targets and signaling pathways,molecular docking was used to evaluate the binding degree between targets and Tec. Western blotting was used to detect the expressions of PI3K/Akt/mTOR pathway related proteins.
Results Tec can inhibit gastric cancer proliferation in a time-dependent and dose-dependent manner,promote the autophagy and apoptosis of HGC-27 cells,up-regulate the protein expressions of autophagy factor Beclin-1,apoptosis factor p53 and Bax,and reduce the protein expressions of apoptosis molecule Bcl-2. PPI network visualization analysis showed a strong affinity between Tec and targets such as AKT1,while KEGG enrichment analysis suggested that the inhibitory effect of Tec on gastric cancer may be closely related to the PI3K/Akt/mTOR signaling pathway. The protein expressions of the PI3K/Akt/mTOR signaling pathway,including p-PI3K,p-Akt and p-mTOR,were down-regulated.
Conclusion Tec can induce the cell apoptosis and autophagy through the PI3K/Akt/mTOR pathway to inhibit the growth of HGC-27 cells.
, authors=Xinyu LIU
1, Zhiqiang WANG
2, Ningning YAO
2, Lei HAN
2, Yucheng LU
2, authorsList=Xinyu LIU, Zhiqiang WANG, Ningning YAO, Lei HAN, Yucheng LU, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1317125612129604543, articleId=1317125611609510845, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=射干苷通过PI3K/Akt/mTOR信号通路诱导胃癌HGC-27细胞凋亡和自噬, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的 探讨射干苷(Tectoridin,Tec)对人胃癌细胞HGC-27细胞自噬和凋亡的影响。
方法 采用CCK-8和克隆形成检测细胞增殖能力,流式细胞术检测细胞凋亡率,自噬抑制剂3-甲基腺嘌呤(3-MA)用于检测自噬;蛋白免疫印迹法检测Beclin-1、Bcl-2、Bax和p53的蛋白表达;进行生物信息学方法预测其可能的靶点及信号通路,分子对接用于评估靶点与Tec的结合程度;蛋白免疫印迹法检测相关蛋白的表达水平。
结果 Tec以时间和剂量依赖的方式抑制胃癌HGC-27细胞增殖,促进细胞的自噬和凋亡,上调自噬因子Beclin-1、凋亡因子p53、BAX的蛋白表达,减少凋亡分子Bcl-2的蛋白表达。蛋白互作(protein-protein interaction,PPI)网络可视化分析显示Tec与AKT1等靶点的亲和力强,KEGG富集分析表明Tec抑制胃癌的作用机制可能与PI3K/Akt/mTOR信号通路密切相关;PI3K/Akt/mTOR信号通路p-PI3K、p-Akt、p-mTOR的蛋白表达下调。
结论 Tec可以通过抑制PI3K/Akt/mTOR通路诱导细胞凋亡和自噬来抑制HGC-27细胞的生长。
, authors=刘鑫雨
1, 王志强
2, 姚宁宁
2, 韩磊
2, 陆玉成
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