Article(id=1291404560728318716, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1291404554201985968, articleNumber=null, orderNo=null, doi=10.13699/j.cnki.1001-6821.2025.06.008, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1723651200000, receivedDateStr=2024-08-15, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1785824440413, onlineDateStr=2026-08-04, pubDate=1743091200000, pubDateStr=2025-03-28, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1785824440413, onlineIssueDateStr=2026-08-04, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1785824440413, creator=13701087609, updateTime=1785824440413, updator=13701087609, issue=Issue{id=1291404554201985968, tenantId=1146029695717560320, journalId=1246415772164075586, year='2025', volume='41', issue='6', pageStart='751', pageEnd='900', issueExtLink='null', onlineDate='null', pubDate='1743091200000', pubDateStr='2025-03-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1785824438858, creator='13701087609', updateTime=1785824438858, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext=null, issueFiles=null, downloadFileDto=null}, startPage=790, endPage=793, ext={EN=ArticleExt(id=1291404560921256701, articleId=1291404560728318716, tenantId=1146029695717560320, journalId=1246415772164075586, language=EN, title=
MiR-28-5
p targeting GAGE12I inhibits gastric cancer cell proliferation, migration and invasion
in vitro, columnId=1246531407326105792, journalTitle=Chinese Journal of Clinical Pharmacology, columnName=Clinical and Basic Bridging Research, runingTitle=null, highlight=null, articleAbstract=
Objective To investigate the in vitro inhibitory effects of microRNA-28-5p (miR-28-5p) targeting G antigen 12I antibody (GAGE12I) on the proliferation, migration, and invasion of gastric cancer cells.
Methods SGC-7901 cell were randomly divided into miR-28-5p group (miR-28-5p mimic), miR-NC group (miR-28-5p negative control mimic), shGAGE12I group (GAGE12I knockout) and blank group (GAGE12I not knockout). Cell proliferation, migration, and invasion capabilities were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay and invasion chambers. Bioinformatics analysis and luciferase activity assays were conducted to examine the interaction between miR-28-5p and GAGE12I.
Results The proliferation rates of miR-28-5p and miR-NC groups were (99.90±10.30)% and (48.25±4.15)%; the invasion rates were (145.57±14.52)% and (67.30±6.95)%; the mobility rates were (103.58±10.75)% and (43.18±4.26)%, respectively, the differences were statistically significant (all P<0.05). The proliferation rates of shGAGE12I group and blank group were (99.80±10.20)% and (35.50±3.58)%; the invasion rates were (142.70±13.65)% and (65.30±6.75)%; the mobility rates were (103.55±10.06)% and (48.38±4.52)%, respectively, the differences were statistically significant (all P<0.05). GAGE12I was the target of miR-28-5p.
Conclusion MiR-28-5p negatively regulates GAGE12I and reduces the proliferation, invasion and migration of gastric cancer cells.
, authors=Li-ping XIAO
1, Qing-fang ZENG
2, Tao ZHAN
3, authorsList=Li-ping XIAO, Qing-fang ZENG, Tao ZHAN, authorCompany=null, correspAuthors=Qing-fang ZENG, 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=1291404561214857982, articleId=1291404560728318716, tenantId=1146029695717560320, journalId=1246415772164075586, language=CN, title=靶向GAGE12I的
miR-28-5
p体外抑制胃癌细胞增殖、迁移和侵袭的研究, columnId=1246531407485489349, journalTitle=中国临床药理学杂志, columnName=临床与基础桥接研究, runingTitle=null, highlight=null, articleAbstract=
目的 探讨靶向G抗原12I抗体（GAGE12I）的微小核糖核酸-28-5p（miR-28-5p）对体外抑制胃癌细胞增殖、迁移和侵袭的影响。
方法 将SGC-7901细胞分为miR-28-5p组（miR-28-5p模拟物）、miR-NC组（miR-28-5p空白模拟物）、shGAGE12I组（GAGE12I敲除）、空白组（GAGE12I未敲除）。用四甲基偶氮唑盐比色法和侵袭实验小室检测细胞的增殖、迁移和侵袭能力，用生物信息学分析和荧光素酶活性检测miR-28-5p与GAGE12I的相互作用。
结果 miR-28-5p组与miR-NC组的增殖率分别为（99.90±10.30）%和（48.25±4.15）%，侵袭率分别为（145.57±14.52）%和（67.30±6.95）%，迁移率分别为（103.58±10.75）%和（43.18±4.26）%，在统计学上差异均有统计学意义（均P<0.05）。shGAGE12I组和空白组的增殖率分别为（99.80±10.20）%和（35.50±3.58）%，侵袭率分别为（142.70±13.65）%和（65.30±6.75）%，迁移率分别为（103.55±10.06）%和（48.38±4.52）%，在统计学上差异均有统计学意义（均P<0.05）。GAGE12I为miR-28-5p的靶标。
结论 miR-28-5p负调控GAGE12I，减少胃癌细胞的增殖、侵袭和迁移。
, authors=肖丽萍
1, 曾庆芳
2, 詹涛
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肖丽萍（1977-），女，副主任护师，主要从事肿瘤护理方面的工作
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