期刊文献+

宫颈癌组织中DNA甲基转移酶1、3A和3B mRNA的表达 被引量:5

Expression of DNMT1,3A and 3B mRNA in uterine cervical carcinoma tissue
下载PDF
导出
摘要 目的探讨DNA甲基转移酶1、3A和3B在宫颈癌发生发展中的作用。方法应用real-time PCR技术检测10例宫颈癌、10例宫颈上皮内瘤变和10例正常宫颈组织DNMT1、3A和3BmRNA的表达。结果宫颈癌组织、宫颈上皮内瘤变和正常宫颈中DNMT 1mRNA对GAPDH mRNA的相对丰度值分别是0.30±0.1、0.26±0.12和0.10±0.04,宫颈癌组织组织中与正常宫颈中DNMT 1表达有显著差异(P<0.05);宫颈癌组织、宫颈上皮内瘤变和正常宫颈中DNMT3A mRNA对GAPDH mRNA的相对丰度值分别是0.94±0.27、0.51±0.24和0.13±0.04,三组相比较有显著性差异(P<0.05);宫颈癌组织、宫颈上皮内瘤变和正常宫颈中DNMT 3B mRNA对GAPDH mR-NA的相对丰度值分别是0.30±0.09、0.28±0.11和0.11±0.04,宫颈癌组织组织中与正常宫颈中DNMT 3B表达有显著差异(P<0.05)。结论 DNMT1、3A和3B参与了宫颈癌的发生,并在宫颈上皮内瘤变时就已经起了一定作用。 Objective: To study the relationship between DNMT1,3A and 3BmRNA expression and oncogenesis of uterine cervical carcinoma.Methods: The expressions of DNMT1,3A and 3B mRNA were detected by real-time PCR in 10 cases of cervical carcinoma,10 cases of cervical intraepithelial neoplasia(CIN) and 10 cases of normal cervical tissue.Results: The relative abundance of DNMT 1mRNA to GAPDH mRNA in cervical carcinoma,in CIN and in normal cervica were 0.30±0.1,0.26±0.12 and 0.10±0.04 respectively.The DNMT 1 mRNA was found to be increased in cervical carcinoma(P0.05,vs normal cervical tissue).The relative abundance of DNMT 3A?mRNA to GAPDH mRNA in cervical carcinoma,in CIN and in normal cervica were 0.94±0.27,0.51±0.24 and 0.13±0.04,respectively.There were significant differences among three groups(P0.05).The relative abundance of DNMT 3B mRNA to GAPDH mRNA in cervical carcinoma,in CIN and in normal cervica were 0.30±0.09,0.28±0.11 and 0.11±0.04 respectively.The DNMT 3B mRNA was found to be increased in cervical carcinoma(P0.05,vs normal cervical tissue) Conclusion: Progressively increasing expressions of DNMT1,DNMT 3A and 3B are associated with cervical carcinogenesis even during the precancerous stages.
出处 《泰山医学院学报》 CAS 2011年第5期321-323,共3页 Journal of Taishan Medical College
基金 国家自然科学基金资助项目(81060212) 内蒙古自然科学基金资助项目(2010BS1104) 中国博士后基金项目(20080430851)
关键词 宫颈肿瘤 宫颈上皮内瘤变 DNA甲基转移酶1 DNA甲基转移酶3A DNA甲基转移酶3B cervical carcinoma cervical intraepithelial neoplasia DNMT1 DNMT3A DNMT3B
  • 相关文献

参考文献9

  • 1Virmani AK,Muller C,Rathi A,et al.Aberrant methylation during cervical carcinogenesis[J].Clin Cancer Res,2001,7:584-589.
  • 2Sova P,Feng Q,Geiss G,et al.Discovery of novel methylation biomarkers in cervical carcinoma by global demethylation and microarray analysis[J].Cancer Epidemiol Biomarkers Prev,2006,15:114-123.
  • 3Robertson KD,Uzvolgyi E,Liang G,et al.The human DNA methyltransferases (DNMTs) 1,3a and 3b:coordinate mRNA expression in normal tissues and overexpression in tumors[J].Nucleic Acids Res,1999,27:2291-2298.
  • 4Bestor TH.The DNA methyltransferases of mammals[J].Hum Mol Genet,2000,9:2395-2402.
  • 5Van Emburgh BO,Robertson KD.Modulation of Dnmt3b function in vitro by interactions with Dnmt3L,Dnmt3a and Dnmt3b splice variants[J].Nucleic Acids Res,2011.
  • 6赵先兰,饶燕玲,孟志英,乔玉环.宫颈癌组织中DNA甲基转移酶1mRNA的表达[J].郑州大学学报(医学版),2009,44(1):120-122. 被引量:4
  • 7Zhao S,Sun G,Tony PW,et al.Expression and methylation status of the Syk gene in cervical carcinoma[J].Arch Gynecol Obstet,2011,283:1113-1119.
  • 8Rizvi MM,Alam MS,Ali A,et al.Aberrant promoter methylation and inactivation of PTEN gene in cervical carcinoma from Indian population[J].J Cancer Res Clin Oncol,2011,137:1255-1262.
  • 9Terra AP,Murta EF,Maluf PJ,et al.Aberrant promoter methylation can be useful as a marker of recurrent disease in patients with cervical intraepithelial neoplasia grade Ⅲ[J].Tumori,2007,93:572-579.

二级参考文献10

  • 1Kang S,Kim JW,Kang GH,et al. Comparison of DNA hypermethylation patterns in different types of uterine cancer: cervical squamous cell carcinoma, cervical adenocarcinonla and endometrial adenocarcinoma [ J ]. Int J Cancer, 2006, 118(9) :2 168.
  • 2Nakagawa T, Kanai Y, Ushijima S, et al. DNA hypermethylation on multiple CpG islands associated with increased DNA methyltransferase DNMT1 protein expression during multistage urothelial carcinogenesis [ J ]. J Urol,2005,173 (5) :1 767.
  • 3Etoh T, Kanai Y, Ushijima S, et al. Increased DNA methyhransferase 1 ( DNMT1 ) protein expression correlates significantly with poorer tumor differentiation and frequent DNA hypermethylation of multiple CpG islands in gastric cancers [ J ]. Am J Pathol,2004,164 (2) :689.
  • 4Li E. Chromatin modification and epigenetic reprogramming in mammalian development [ J ]. Nat Rev Genet, 2002,3 (9) :662.
  • 5Bestor TH. The DNA methyhransferases of mammals [ J]. Hum Mol Genet,2000,9(16) :2 395.
  • 6Fang JY, Lu R, Mikovits JA, et al. Regulation of hMSH2 and hMLH1 expression in the human colon cancer cell line SW1116 by DNA methylteansferase 1 [ J ]. Cancer Let, 2006,233(1 ) :124.
  • 7Kassis ES, Zhao M, Hong JA, et al. Depletion of DNA methyhransferase 1 and/or DNA methyhransferase 3b mediates'growth arrest and apoptosis in lung and esophageal cancer and malignant pleural mesothelioma cells [ J ]. J Thorac Cardiovasc Surg, 2006,131 ( 2 ) :298.
  • 8Szyf M. The role of DNA methyltransferase 1 in growth control [ J ]. Front Biosci ,2001 , 6 : D599.
  • 9Kong WJ,Zhang S, Guo CK, et al. Effect of methylation-associated silencing of the death-associated protein kinase gene on nasopharyngeal carcinoma[ J]. Anticancer Drugs, 2006,17(3) :251.
  • 10Kantarjian HM, O-Brich SH, Estey E, et al. Decitabine studies in chronic and acute myelogenous leukemia [ J]. Leukemia, 1997,11 ( Suppl 1 ) : S35.

共引文献3

同被引文献40

  • 1Vasiliki Psofaki,Chryssoula Kalogera,Nikolaos Tzambouras,Dimitrios Stephanou,Epameinondas Tsianos,Konstantin Seferiadis,Georgios Kolios.Promoter methylation status of hMLH1,MGMT,and CDKN2A/p16 in colorectal adenomas[J].World Journal of Gastroenterology,2010,16(28):3553-3560. 被引量:14
  • 2丁青,顾美皎.早期宫颈癌根治性宫颈切除术术式及其术后复发和妊娠结局[J].中国实用妇科与产科杂志,2004,20(7):437-439. 被引量:6
  • 3马刚,张浩,董明,郑新宇,尾崎岩太,松桥幸子,郭克建.程序性细胞死亡因子4在消化系统肿瘤中表达及其与肿瘤分化的关系[J].中华肿瘤防治杂志,2007,14(4):249-253. 被引量:9
  • 4Yang Q, Shah L, Yoshimura G, et al. 5-aza-2"-deoxycytidine in-duces retinoie acid receptor beta 2 demethylation, cell cycle arrest and growth inhibition in breast carcinoma cells [ J ]. Anticancer Research, 2002, 22 (5):2753-2756.
  • 5Vidaurreta M, Maestro ML, Sanz-Casla MT, et al. Inactivation of p16 by CpG hypermethylation in renal cell carcinoma[ J]. Urolog- ic Oncology, 2008, 26 (3) :239 -245.
  • 6Avissar- Whiting M, Koestler DC, Houseman EA, et al. Poly- comb group genes are targets of aberrant DNA methylation in renal cell carcinoma[J]. Epigenetics, 2011,6 (6) :703 -709.
  • 7Kawakami T, Okamoto K, Ogawa O, et al. Muhipoint methylation and expression analysis of tumor suppressor genes in human renal cancer cells[J]. Urology, 2003, 61 ( 1 ) :226 -230.
  • 8Morris MR, Hesson LB, Wagner KJ, et 81. Multigene methylation analysis of Wilms'tumour and adult renal cell carcinoma[ J]. On- cogene, 2003, 22 (43):6794-6801.
  • 9Patel K, Dickson J, Din S, et al. Targeting of 5-aza-2"-deoxycyti- dine residues by chromatin-associated DNMT1 induces proteasomal degradation of the free enzyme [ J ]. Nucleic Acids Research, 2010, 38 (13) :4313 -4324.
  • 10Maslov AY, Lee M, Gundry M, et al. 5-Aza-2"-deoxycytidine-in- duced genome rearrangements are mediated by DNMT1 [J]. Onco- genc, 2012, 31 (50) :5172 -5179.

引证文献5

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部