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原发性肝细胞癌中DNMT3b基因剪接变异体的表达分析

Analysis of Splice Variants of DNMT3b Gene in Primary Hepatocellular Carcinoma
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摘要 目的:研究原发性肝癌中DNMT3b基因剪接变异体的表达情况及其在肝癌发生发展中的作用。方法:通过RT-PCR的方法对30例肝癌、30例癌旁组织中DNMT3b基因的剪接变异体进行检测,并将结果与肝癌患者临床指标进行统计学分析。结果:RT-PCR结果显示DNMT3b基因以四种剪接变异体(DNMT3b1、DNMT3b3、DNMT3b4和DNMT3b5)的形式表达,其总的表达率肝癌组为93.3%(28/30),癌旁组为93.3%(28/30)。其中DNMT3b4在肝癌组中的表达高于癌旁组(P<0.05),与肝癌病理分化和CLIP评分无相关性(P>0.05)。结论:DNMT3b基因剪接变异体DNMT3b4可能参与肝癌的发生演变。 Objective: To study the splice variants of DNMT3b gene in primary hepatocellular carcinoma, and their effects on the development of hepatocellular carcinoma. Methods: Thirty hepatocellular carcinoma (HCC) tissues and their corresponding adjacent para-cancerous tissues were examined. RT-PCR was used to detect the splice variants of DNMT3b gene. The relationship between the laboratory results and clinicopathological characteristics of HCC was analyzed as well. Results: The expressions of DNMT3b gene were detected by RT-PCR in the forms of alternative spliced variants of DN- MT3b1, DNMT3b3, DNMT3b4 and DNMT3b5. Their total expressions were 93.3% (28/30) in HCC and 93.3% (28/30)in para-cancerous tissues. There was a higher DNMT3b4 expression in HCC than that in para-cancerous tissues (P〈0.05). There was no relationship between pathological differentiation and CLIP grade (P〉0.05). Conclusion: DNMT3b4, one of the alternative spliced forms of DNMT3b, may play an important role in hepatic carcinogenesis.
出处 《天津医药》 CAS 北大核心 2008年第1期1-3,共3页 Tianjin Medical Journal
基金 天津市科委科技攻关项目(项目编号:05YFSJSF02500) 天津市科委科技创新能力与环境建设平台项目(项目编号:05SYSYJC02600)
关键词 肝肿瘤 剪接体 立体异构现象 基因表达 liver neoplasms carcinoma spliceosomes stereoisomerism gene expression
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参考文献8

  • 1Shames DS, Minna JD, Gazdar AF, et al. DNA methylation in health,disease, and cancer[J]. Curr Mol Med, 2007,7( 1 ) : 85-102.
  • 2Yoshikawa H. DNA methylation and cancer [J]. Gan To Kagaku Ryoho, 2007,34(2) : 145-149.
  • 3Park HJ,Yu E,Shim YH. DNA methyltransferase expression and DNA hypermethylation in human hepatocellular carcinoma [J]. Cancer Lett,2006,233(2) :271-278.
  • 4Beaulieu N,Morin S,Chute IC,et al. An essential role for DNA methytransferase DNMT3B in cancer cell survival [J]. J Biol Chem, 2002,277(31 ) :28176-28181.
  • 5Luczak MW, Jagodzinski PP. The role of DNA methylation in cancer development[J]. Folia Histochem Cytobiol, 2006,44(3 ) : 143-154.
  • 6Saito Y,Kanai Y,Sakamoto M,et al. Overexpression of a splice variant of DNA methyltransferase 3b,DNMT3b4,associated with DNA hypomethylation on pericentromeric satellite regions during human hepatoearcino genesis[J]. PNAS, 2002,99:10060-10065.
  • 7Kanai Y, Saito Y, Ushijima S, et al. Alterations in gene expression associated with the overexpression of a splice variant of DNA methyhransferase 3b, DNMT3b4, during human hepatocarcinogenesis[J]. J Cancer Res Clin Oncol, 2004,130( 11 ) : 636-644.
  • 8Brueckner B, Kuck D, Lyko F. DNA methyltransferase inhibitors for cancer therapy[J]. Cancer J, 2007,13( 1 ) : 17-22.

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