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miR-142-3p表达对卵巢癌SKOV3细胞生长和转移的影响 被引量:3

Effect of miR-142-3p Expression on Growth and Metastasis of SKOV3 Ovarian Cancer Cells
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摘要 目的探讨miR-142-3p表达对卵巢癌SKOV3细胞生长和转移的影响。方法收集40例卵巢癌患者标本,同时收集20例相应的癌旁组织。利用荧光定量PCR方法检测各组织中miR-142-3p表达水平。用脂质体作为载体将miR-142-3p模拟物转染至SKOV3细胞,应用实时PCR和Western blotting方法检测正常与与转染的SKOV3细胞HMGA2 mRNA及蛋白表达情况。结果miR-142-3p在卵巢癌组织中表达水平明显高于癌旁组织(P<0.01)。过表达miR-142-3p能够抑制HMGA2 mRNA和蛋白表达(P<0.05)。过表达miR-142-3p显著抑制SKOV3细胞生长和转移。结论miR-142-3p表达增加能够抑制SKOV3细胞中HMGA2 mRNA和蛋白表达,并抑制SKOV3细胞的生长和转移。 Objective To study the effects of miR-142-3p expression on the growth and metastasis of SKOV3 ovarian cancer cells.Methods Forty specimens from ovarian cancer patients were collected,with 20 corresponding adjacent tissue samples collected simul-taneously.The expression level of miR-142-3p in various tissues was determined by real-time quantitative PCR.miR-142-3p mimics were transfected into SKOV3 cells using a liposome vector.Real-time PCR and Western blotting were used to detect the expression of miR-142-3p in normal SKOV3 and transfected HMGA2 cells.Results The level of expression of miR-142-3p in ovarian cancer tissues was significantly higher than that of the adjacent tissues(P<0.01).Overexpression of miR-142-3p could inhibit the expression of HMGA2 mRNA and protein(P<0.05);additionally,this overexpression significantly inhibited the growth and metastasis of SKOV3 cells.Con-clusion Overexpression of miR-142-3p can inhibit the expression of both HMGA2 mRNA and protein,as well as inhibit the growth and metastasis of SKOV3 cells.
作者 陆晓云 张斌 佟芳 LU Xiaoyun;ZHANG Bin;TONG Fang(Department of Gynaecology and Obstetrics,The First Affiliated Hospital of Dalian Medical University,Dalian 116011,China;Department of Oncology,The First Affiliated Hospital of Dalian Medical University,Dalian 116011,China)
出处 《中国医科大学学报》 CAS CSCD 北大核心 2019年第9期817-821,共5页 Journal of China Medical University
基金 辽宁省高等学校基本科研项目(LQ2017024)
关键词 miR-142-3p 卵巢癌 SKOV3细胞 生长 转移 miR-142-3p ovarian cancer SKOV3 cells growth metastasis
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  • 1Odgaard A O,Koh W P,Yuan J M.Combined lifestyle factors and risk of incident colorectal cancer in a chinese population[J].Can- cer Prey Res(Phila), 2013, 6(4):360-367.
  • 2Langan R C,Mullinax J E,Raiji M T, et aI.Colorectal cancer biomar - kers and the potential role of cancer stem cells[J].J Cancer, 2013, 4(3): 241-250.
  • 3Backman V,Roy H K.Advances in biophotonics detection of field carcinogenesis for colon cancer risk stratification[J].J Cancer, 2013, 4(3):251-261.
  • 4Krek A,Gr u n D,Poy M N ,et aI,Combinatorial microRNA target predictions[J].Nat Genet,2005,37(5):495-500.
  • 5Mirnezami A H,Pickard K,Zhang L, et aI.MicroRNAs: Key players in carcinogenesis and novel therapeutic targets[J].Eur J Surg Oncol, 2009, 35(4):339-347.
  • 6He L,Thomason J M,Hemann M T,et aI.A microRNA polycistron as a potential human oncogene [J ]. Nature, 2005,435 ( 7043): 828-833.
  • 7Li J M,Zhao R H,Li S T,et aI.Down-regulation of fecal miR-143 and miR-145 as potential markers for colorectal cancer[J].Sandi Med J, 2012, 33(1):24-29.
  • 8Nugent M,Miller N,Kerin M J.MicroRNAs in colorectal cancer: function, dysregulation and potential as novel biomarkers[J].Eur J Surg Oncol, 2011, 37(8): 649-654.
  • 9Chen X,Guo X,Zhang H,et aI.Role of miR-143 targeting KRAS in colorectal tumorigenesis[J].Oncogene,2009,28(10): 1385-1392.
  • 10Luo H,Zou J,Dong Z,et al.Up-regulated miR-17 promotes cell proliferation, tumour growth and cellcycle progression by tar- geting the RND3 tumour suppressor gene in colorectal carci- noma[J].Bioohem J, 2012, 442(2):311-321.

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