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miR-1205/DNAJB1 reverses docetaxel chemoresistance in human triple negative breast carcinoma cells via regulation of mutp53/TAp63 signaling
文献摘要:
Chemoresistance is the major cause of therapeutic failure in human triple negative breast carcinoma(TNBC).Docetaxel(DOC),a first-line therapeutic drug in TNBC treatment,is limited for long-term use due to the develop-ment of chemoresistance.Thus,overcoming chemoresistance of DOC remains an important challenge to improve patient's outcome of TNBC.In this study,we aimed to investigate the molecular mechanism behind DOC che-moresistance and the possible therapeutic effects of miRNAs.Utilizing qRT-PCR analysis,we discovered that miR-1205 is gradually downregulated in human triple negative breast carcinoma MDA-MB-231 and docetaxel-resistant MDA-MB-231(MDA-MB-231/DOC)cells compared with Hs 578Bst normal human breast fibroblasts.Cell viability,cell cycle and apoptosis assays in MDA-MB-231/DOC cells indicated that miR-1205 overexpression enhances doc-etaxel sensitivity by reducing cell viability as well as inducing G2/M cell cycle arrest and cell apoptosis.Western blot analysis,dual-luciferase reporter assay,co-immunoprecipitation assay and chromatin immunoprecipitation assay revealed that miR-1205 overexpression disrupts the stable complex formation of DNAJB1,mutp53 and TAp63 by directly reducing DNAJB1 expression,which abates the sequestrating effect of mutp53 on TAp63,thereby leading to the enhanced DOC sensitivity in MDA-MB-231/DOC cells.Our findings demonstrate the role of the miR-1205/DNAJB1 axis in the docetaxel resistance of TNBC,which may offer a promising therapeutic approach to resolve docetaxel resistance in TNBC.
文献关键词:
作者姓名:
Yongxiang Yin;Jinqiu Zhang;Tao Ma;Daozhen Chen;Daru Lu
作者机构:
State Key Laboratory of Genetic Engineering and MOE Engineering Research Center of Gene Technology,School of Life Sciences,Fudan University,Shanghai 200438,China;Department of Pathology,The Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University,Wuxi 214002,China;Department of Breast,The Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University,Wuxi 214002,China;Central Laboratory,The Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University,Wuxi 214002,China
引用格式:
[1]Yongxiang Yin;Jinqiu Zhang;Tao Ma;Daozhen Chen;Daru Lu-.miR-1205/DNAJB1 reverses docetaxel chemoresistance in human triple negative breast carcinoma cells via regulation of mutp53/TAp63 signaling)[J].生物化学与生物物理学报(英文版),2022(01):37-46
A类:
mutp53,Chemoresistance,moresistance,578Bst,etaxel,abates,sequestrating
B类:
DNAJB1,reverses,docetaxel,chemoresistance,human,triple,negative,breast,carcinoma,cells,regulation,TAp63,signaling,major,cause,therapeutic,failure,TNBC,Docetaxel,DOC,first,line,drug,treatment,limited,long,term,due,develop,Thus,overcoming,remains,important,challenge,improve,patient,outcome,In,this,study,aimed,investigate,molecular,mechanism,behind,possible,effects,miRNAs,Utilizing,qRT,analysis,discovered,that,gradually,downregulated,MB,resistant,compared,Hs,normal,fibroblasts,Cell,viability,cycle,apoptosis,assays,indicated,overexpression,enhances,sensitivity,reducing,well,inducing,G2,arrest,blot,luciferase,reporter,immunoprecipitation,chromatin,revealed,disrupts,stable,complex,formation,directly,which,thereby,leading,enhanced,Our,findings,demonstrate,role,axis,may,offer,promising,approach,resolve
AB值:
0.44498
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