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HDAC2 siRNA转染对卵巢癌ovcar3细胞中p53和乙酰化p53k320表达的影响 被引量:3

Effect of HDAC2 siRNA transfection on expression of p53 and acetylated p53k320 in ovarian cancer ovcar3 cells
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摘要 目的:探讨靶向沉默组蛋白去乙酰化酶2(HDAC2)对人卵巢癌ovcar3细胞中p53乙酰化位点k320表达的影响。方法:将ovcar3细胞随机分为空白组、对照组和实验组3组,实验组以HDAC2 siRNA转染细胞,对照组转染对照siRNA,空白组不处理,分别采用实时荧光定量PCR和Western blot方法检测3组细胞中HDAC2 mRNA和蛋白的表达,Western blot检测3组细胞中p53、乙酰化p53k320蛋白的表达。结果:与空白组及对照组相比,实验组HDAC2 mRNA和蛋白的表达降低(P<0.05),p53蛋白和乙酰化p53k320蛋白表达均升高(P<0.05)。结论:下调HDAC2的表达可使p53和乙酰化p53k320表达增加。 Aim: To investigate the effect of targeted silencing histone deacetylase 2( HDAC2) on expression of p53 and acetylation p53k320 in human ovarian cancer cell line ovcar3. Methods: ovcar3 cells were divided into 3 groups.HDAC2 siRNA was used to transfected into the ovcar3 cells in experimental group,and the cells transfected with control siRNA( control siRNA group) and the cells without treatment( control group) were the control. Real Time-PCR and Western blot was used to detect the expression of HDAC2 mRNA and protein; the expression of p53 and acethylased p53k320 were examined by Western blot. Results: Compared with control group and control siRNA group,the expressions of HDAC2 mRNA and protein in experimental group were decreased( P〈0. 05),and the expressions of p53 and acethylased p53k320 protein were increased( P〈0. 05). Conclusion: Downregulating the expression of HDAC2 could increase the expressions of p53 and acethylased p53k320.
出处 《郑州大学学报(医学版)》 CAS 北大核心 2016年第3期372-375,共4页 Journal of Zhengzhou University(Medical Sciences)
基金 郑州市科学技术局2015普通科研项目153PKJGG165
关键词 组蛋白去乙酰化酶2 P53 乙酰化p53k320 ovcar3细胞株 卵巢肿瘤 histone deacetylase 2 p53 acetylated p53k320 ovcar3 cells line ovarian neoplasm
作者简介 通信作者,女,1964年9月生,博士,教授,研究方向:妇科肿瘤,E—mail:lihongyu99@qq.com
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  • 1Lefebvre V, Dumitriu B, Penzo-M6ndez A, et al. Control of cell fate and differentiation by Sry-related high-mobility- group box (Sox) transcription factors [ J ]. Int J Biochem Cell Biol,2007,39(12) :2195.
  • 2Kamachi Y, Uchikawa M, Kondoh H. Pairing SOX off: with partners in the regulation of embryonic development [ J ]. Trends Genet,2000,16 (4) : 182.
  • 3Liu KC,Lin BS,Zhao M, et al. The multiple roles for Sox2 in stem cell maintenance and tumorigenesis [ J ]. Cell Sig- nal,2013,25 (5) :1264.
  • 4Lin F,Lin P, Zhao D, et al. Sox2 targets cyclinE, p27 and survivin to regulate androgen-independent human prostate cancer cell proliferation and apoptosis [ J ]. Cell Prolif, 2012,45(3) :207.
  • 5Mukhopadhyay A, Banerjee S, Stafford LJ, et al. Curcumin- induced suppression of cell proliferation correlates with down-regulation of cyclin D1 expression and CDK4-media- ted retinoblastora protein phosphorylation [ J ]. Oncogene, 2002,21 (57) :8852.
  • 6Ji J,Zheng PS. Expression of Sox2 in human cervical carci- nogenesis [ J ]. Hum Pathol,2010,41 ( 10 ) : 1438.
  • 7Neumann J, Bahr F,Horst D, et al. SOX2 expression corre- lates with lymph-node metastases and distant spread in right-sided colon cancer[ J]. BMC Cancer,2011 , 11:518.
  • 8Chert YP, Shi L, Zhang L,et al. The molecular mechanism governing the oncogenic potential of SOX2 in breast cancer [J]. J Biol Chem,2008,283(26) :17969.
  • 9Lu Y,Futtner C, Rock JR,et al. Evidence that SOX2 over- expression is oncogenic in the lung[J]. PLoS One,2010,5 (6) :e1 1022.
  • 10Basu M, Roy SS. Wnt/-catenin pathway is regulated by PITX2 homeodomain protein and thus contributes to the proliferation of human ovarian adenocarcinoma cell,SKOV- 3[J]. J Biol Chem 2013 ,288(6) :4355.

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