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外泌体lncRNA CIAT1促进膀胱癌集体侵袭的机制

刘志聪 刘戴胤 龙钧天 成炽杏 黄健

实用医学杂志2025,Vol.41Issue(9):1299-1308,10.
实用医学杂志2025,Vol.41Issue(9):1299-1308,10.DOI:10.3969/j.issn.1006-5725.2025.09.005

外泌体lncRNA CIAT1促进膀胱癌集体侵袭的机制

Exosomal lncRNA CIAT1 promotes collective invasion of bladder cancer

刘志聪 1刘戴胤 1龙钧天 2成炽杏 1黄健1

作者信息

  • 1. 中山大学孙逸仙纪念医院泌尿外科(广东 广州 510030)||广东省恶性肿瘤表观遗传与基因调控重点实验室(广东 广州 510030)
  • 2. 广东省恶性肿瘤表观遗传与基因调控重点实验室(广东 广州 510030)||中山大学孙逸仙纪念医院肿瘤科(广东 广州 510030)
  • 折叠

摘要

Abstract

Objective To investigate the role and molecular mechanisms of bladder cancer-derived exosomal long non-coding RNA(lncRNA)CIAT1 in mediating collective invasion and to evaluate its clinical significance and potential therapeutic value.Methods High-throughput sequencing was used to identify lncRNAs that are highly expressed in exosomes from bladder cancer and lymph node metastatic tissues.CIAT1 was selected for further validation in clinical bladder cancer samples.By constructing CIAT1-overexpressing and knockdown bladder cancer cells,we demonstrated in vitro that CIAT1-contained exosomes target cancer-associated fibroblasts(CAFs)to induce collective invasion.The underlying mechanism of CIAT1 in bladder cancer collective invasion was explored through RNA pull-down,RNA immunoprecipitation(RIP),dual-luciferase reporter assays,chromatin isolation by RNA purification(ChIRP)and chromatin immunoprecipitation(ChIP).Results CIAT1 was significantly upregulated in exosomes derived from bladder cancer tissues compared to adjacent normal tissues by High-throughput sequencing(fold change>1.5,P<0.05)and clinical sample validation(P<0.01).In vitro experiments,exosomal CIAT1 was selectively internalized by cancer-associated fibroblasts(CAFs),significantly enhancing collective invasion of bladder cancer via regulating CAFs.In co-culture models,CIAT1 overexpression group showed increased total number and total length of collective invasion chains compared to the control group(P<0.01 for both).Mechanistically,CIAT1 was packaged into exosomes via binding to hnRNPA2B1,and internalized by CAFs,where it activated N-cadherin transcription by modulating H3K4me3 histone modification at the N-cadherin promoter.Consistently,the CIAT1 overexpression group exhibited elevated collective invasion chain numbers and lengths compared to the control group(P<0.01 for both).However,blocking N-cadherin reversed the pro-invasive effects of CIAT1,with no significant differences in chain numbers or lengths between the CIAT1 overexpression+N-cadherin blockade group and controls(P>0.05 for both).Further clinical correlation analysis confirmed that CIAT1-regulated N-cadherin is closely associated with collective invasion in bladder cancer patients(P<0.01).Conclusions Exosomal CIAT1 derived from bladder cancer cells targets CAFs to activate N-cadherin transcription,thereby promoting bladder cancer collective invasion.

关键词

膀胱癌/外泌体/lncRNA/集体侵袭

Key words

bladder cancer/exosomes/lncRNA/collective invasion

分类

临床医学

引用本文复制引用

刘志聪,刘戴胤,龙钧天,成炽杏,黄健..外泌体lncRNA CIAT1促进膀胱癌集体侵袭的机制[J].实用医学杂志,2025,41(9):1299-1308,10.

基金项目

国家自然科学基金项目(编号:82173230) (编号:82173230)

实用医学杂志

OA北大核心

1006-5725

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