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首页|期刊导航|中国肿瘤生物治疗杂志|lncRNA PTENP1通过调控SCARA5表达对膀胱癌细胞恶性生物学行为的影响及其可能的机制

lncRNA PTENP1通过调控SCARA5表达对膀胱癌细胞恶性生物学行为的影响及其可能的机制

王静 孙颖 周敏 赵其波 杨猛 黄子明

中国肿瘤生物治疗杂志2025,Vol.32Issue(11):1151-1158,8.
中国肿瘤生物治疗杂志2025,Vol.32Issue(11):1151-1158,8.DOI:10.3872/j.issn.1007-385x.2025.11.007

lncRNA PTENP1通过调控SCARA5表达对膀胱癌细胞恶性生物学行为的影响及其可能的机制

Effects and mechanisms of lncRNA PTENP1 on proliferation,apoptosis,migration,and invasion of bladder cancer cells by regulating SCARA5 expression

王静 1孙颖 1周敏 1赵其波 1杨猛 2黄子明3

作者信息

  • 1. 江苏食品药品职业技术学院 制药工程学院,江苏 淮安 223005
  • 2. 江苏食品药品职业技术学院 健康医学院,江苏 淮安 223005
  • 3. 南京医科大学附属淮安第一人民医院 急诊科,江苏 淮安 223002
  • 折叠

摘要

Abstract

Objective:To investigate the functional mechanism of bone marrow mesenchymal stem cell(BMSC)-derived exosome lncRNA PTENP1 in bladder cancer progression.Methods:Exosomes from BMSC(BMSC-Exo)were characterized using transmission electron microscopy,nanoparticle tracking analysis(NTA),and WB assay for exosomal markers.The uptake of exosomes derived from BMSC by bladder cancer 5637 cells was confirmed through confocal microscopy.Based on different transfectants,bladder cancer cells(5637 and T24)were divided into groups:control group(no exosomes),BMSC-Exo group,BMSC OE-NC-Exo group,BMSC OE-PTENP1-Exo group,BMSC sh-NC-Exo group,and BMSC sh-PTENP1-Exo group,and co-cultured with respective exosomes(20 μg/mL).The evaluation of cell proliferation,apoptosis,migration,and invasion was conducted using CCK-8,colony formation,flow cytometry,wound healing,and Transwell assays,respectively.The interactions involving miR-17 with PTENP1 and scavenger receptor class A member 5(SCARA5)were validated using dual luciferase reporter assays,RNA pull-down,and RNA immunoprecipitation(RIP)methods.Results:qRT-PCR showed that BMSC exosomes overexpressing PTENP1(BMSC OE-PTENP1-Exo)significantly elevated PTENP1 levels in bladder cancer cells(P<0.01).BMSC OE-PTENP1-Exo inhibited cell proliferation(P<0.01),migration(P<0.01),and invasion(P<0.01),and promoted cell apoptosis(P<0.01).Furthermore,in vivo experiments showed that BMSC OE-PTENP1-Exo significantly inhibited tumor growth in nude mice(P<0.01).Conclusion:BMSC-derived exosomal PTENP1 inhibits BC progression by upregulating the expression of SCARA5 via sponging miR-17,providing a potential new therapeutic target for bladder cancer bladder cancer treatment.

关键词

lncRNA PTENP1/A类清道夫受体 5型/膀胱癌/5637细胞/T24细胞/增殖/凋亡

Key words

lncRNA PTENP1/scavenger receptor class A member 5(SCARA5)/bladder cancer/5637 cell/T24 cell/proliferation/apoptosis

分类

医药卫生

引用本文复制引用

王静,孙颖,周敏,赵其波,杨猛,黄子明..lncRNA PTENP1通过调控SCARA5表达对膀胱癌细胞恶性生物学行为的影响及其可能的机制[J].中国肿瘤生物治疗杂志,2025,32(11):1151-1158,8.

基金项目

江苏高校"青蓝工程"项目[苏教师函[2022]29号 ()

苏教师函[2024]14号] ()

淮安市自然科学研究计划(No.HAB202146) (No.HAB202146)

中国肿瘤生物治疗杂志

OA北大核心

1007-385X

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