典型文献
DSCR9/miR-21-5p axis inhibits pancreatic cancer proliferation and resistance to gemcitabine via BTG2 signaling
文献摘要:
The outcome of pancreatic adenocarcinoma(PAAD)patients is poor,given resistance to gemcitabine.Long non-coding RNA(IncRNA)has been implicated in the carcinogenesis of pancreatic cancer;however,its function and mechanism in PAAD resistance to gemcitabine(GEM)are yet unknown.Herein,we demonstrate that IncRNA DSCR9 is significantly reduced in PAAD in vitro and in vivo.CCK-8,BrdU and flow cytometry assays show that overexpression of DSCR9 markedly suppresses pancreatic cancer cell proliferation and invasion,and promotes apoptosis under gemcitabine treatment.BTG2 acts as a tumor suppressor by reducing the proliferation and inva-sion of pancreatic cancer cells and increasing gemcitabine-induced apoptosis.Immunofluorescence(IF)staining combined with fluorescence in situ hybridization(FISH)of pancreatic cancer tissues shows that DSCR9 and BTG2 are both increased in pancreatic cancer tissues.Luciferase assay shows that miR-21-5p simultaneously binds to DSCR9 and 3'UTR of BTG2;DSCR9 relieves miR-21-5p-induced inhibition of BTG2 by competing with BTG2 for miR-21-5p binding.Overexpression of miR-21-5p enhances the invasiveness of pancreatic cancer cells by promoting cancer cell proliferation and invasion and attenuating gemcitabine-induced apoptosis.Overexpression of miR-21-5p attenuates the effect of DSCR9 overexpression on BTG2 expression and invasiveness of pancreatic cancer cells.Finally,miR-21-5p expression is increased,while BTG2 expression is decreased in pancreatic cancer tissues.miR-21-5p is negatively correlated with DSCR9 and BTG2.In conclusion,the DSCR9/miR-21-5p/BTG2 axis modulates pancreatic cancer proliferation,invasion,and gemcitabine resistance.
文献关键词:
中图分类号:
作者姓名:
Hui Huang;Xia Li;Xianlin Zhang;Zhiqiang Li;Duo Han;Wenzhe Gao;Ling Liu;Cheng Peng;Hongwei Zhu;Xiao Yu
作者机构:
Department of Hepatopancreatobiliary Surgery,Third Xiangya Hospital,Central South University,Changsha 410013,China;Department of Endocrinology,Third Xiangya Hospital,Central South University,Changsha 410013,China;Department of General Surgery,Affiliated Renhe Hospital of China Three Gorges University,Yichang 443001,China;Department of Cardiology,Second People's Hospital of Hunan Province,Hunan University of Chinese Medicine,Changsha 410007,China
文献出处:
引用格式:
[1]Hui Huang;Xia Li;Xianlin Zhang;Zhiqiang Li;Duo Han;Wenzhe Gao;Ling Liu;Cheng Peng;Hongwei Zhu;Xiao Yu-.DSCR9/miR-21-5p axis inhibits pancreatic cancer proliferation and resistance to gemcitabine via BTG2 signaling)[J].生物化学与生物物理学报(英文版),2022(12):1775-1788
A类:
DSCR9
B类:
miR,5p,axis,inhibits,pancreatic,cancer,proliferation,resistance,gemcitabine,via,BTG2,signaling,outcome,adenocarcinoma,PAAD,patients,poor,given,Long,coding,IncRNA,has,been,implicated,carcinogenesis,however,function,mechanism,GEM,are,yet,unknown,Herein,demonstrate,that,significantly,reduced,vitro,vivo,CCK,BrdU,flow,cytometry,assays,overexpression,markedly,suppresses,invasion,promotes,apoptosis,under,treatment,acts,tumor,suppressor,by,reducing,cells,increasing,induced,Immunofluorescence,IF,staining,combined,situ,hybridization,FISH,tissues,shows,both,increased,Luciferase,simultaneously,binds,UTR,relieves,inhibition,competing,binding,Overexpression,enhances,invasiveness,promoting,attenuating,attenuates,effect,Finally,while,decreased,negatively,correlated,conclusion,modulates
AB值:
0.402696
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