期刊文献+

RUNX3、DNMT1 mRNA在原发性肝细胞癌中的表达及其意义 被引量:1

Expression and Clinical Significance of Runt-related Ttranscription Factor 3 Gene and DNA Methyltransferase 1 in Primary Hepatocellular Carcinoma
下载PDF
导出
摘要 目的研究人RUNT相关转录因子3(Runt-related transcription factor3,RUNX3)和DNA甲基转移酶1(DNA methyltransferase1,DNMT1)在原发性肝细胞癌(primary hepatocellular carcinoma,HCC)中的表达及其与临床病理学特征的关系,并探讨其临床意义。方法应用逆转录聚合酶链反应(Reverse transcription-Poly-merasechain reaction,RT-PCR)检测43例HCC患者癌组织及其相应癌旁组织中RUNX3mRNA、DNMT1mR-NA的表达。结果肝癌组织中RUNX3表达明显降低,DNMT1表达增高;RUNX3表达下调与组织分化程度有关(P<0.05),而与性别、年龄、HBsAg、AFP、静脉癌栓及TNM分期均无明显关系(P>0.05);DNMT1表达升高与静脉癌栓、组织分化程度及TNM分期有关(P<0.05),而与性别、年龄、HBsAg、AFP均无明显关系(P>0.05)。RUNX3与DNMT1表达成负相关(r=-0.2059,P<0.05)。结论RUNX3基因在肝癌组织中表达下调,DNMT1表达增高,可能与肝癌的发生发展有关;高表达的DNMT1在一定程度上参与调控RUNX3基因的表达下调。 Objective To investigate the expression and clinical significance of Runt-related transcription factor 3 gene(Runx3)and DNA methyhransferase 1(Dnmt1) in primary hepatocellular carcinoma (HCC).Methods Reverse transcription-PCR(RT-PCR)was used to detect Runx3 mRNA , Dnmtl mRNA expression level of samples of primary hepatocellular carcinoma and corresponding para-cancer tissue, which were obtained from surgically resection specimens of 43 patients. Results RT-PCR showed that the expression of Runx3 in hepatocellular carcinoma was significantly lower than that in corresponding para-cancer tissue (0.2148 ± 0.0987 vs 0.6013 ±0. 1965, P 〈 0.05) and the expression of Dnmtl in hepatocellular carcinoma was higher than that in corresponding para-cancer tissue(0. 7425±0.4331 vs 0.4911 ±0. 1897, P 〈 0.05). The Down-regulated expression of Runx3 was correlated with pathologic differentiation degree( P 〈 0.05). The up-regulated expression of Dnmtlwas correlated with vein tumor thrombus , TNM stage and pathologic differentiation degree( P 〈 0.05). The relationship between Runx3 and Dnmtl expression was significantly negative ( r = -0. 2059, P 〈 0.05 ). Conclusion The down-regulated expression of Runx3 gene in human hepatocellular carcinoma suggest that Runx3 gene may play an important role in the development and progression of hepatocellular carcinoma. The up-regulated expression of Dnmtl participates to a certain extent degree in the inactivation of Runx3 expression.
出处 《宁夏医科大学学报》 2010年第1期50-53,62,共5页 Journal of Ningxia Medical University
基金 宁夏自然科学基金资助项目(NZ08109)
关键词 原发性肝细胞癌 RUNX3 DNMT1 逆转录聚合酶链反应 primary hepatocellular carcinoma RUNX3 DNMT1 RT-PCR
  • 相关文献

参考文献13

  • 1Moil T, Nomoto S, Koshikawa K, et al. Decreased expression and frequent allelic inactivation of the RUNX3 gene at 1p36 in human hepatocellular carcinoma[ J ]. Liver Int, 2005,25 (2) : 380 - 388.
  • 2Issa JP, Vertino PM, Wu J, et al. Increased cytosine DNA methyltransferase activity during colon cancer progression [J]. Natl Cance RInst, 1993,85(15) :1235 - 1240.
  • 3Li QL, Ito K, Sakaura C, et al. Causal relationship between the loss of RUNY,3 expression and gastric cancer[ J ]. Cell,2002,109:113- 124.
  • 4Fang W, Piao Z, Simon D, et al. Mapping of a minimal deleted region in human hepatocellular carcinoma to 1p36.13- p36.33 and mutational analysis of the RIZ (PRDM2)gene localized to the region. Gene Chromosomes Cancer [ J ]. 2000,28 : 269 - 275.
  • 5张宏,肖文华,梁后杰,房殿春,杨仕明,罗元辉.人DNA MTase反义基因转染诱导E-钙黏附蛋白高表达[J].中华肿瘤杂志,2002,24(5):444-447. 被引量:7
  • 6Bangsow C, Rubins N, Glusman G, et al. The RUNX3 gene -sequence streture and regulated expression [ J]. Gene, 2001,279(2) :221 - 232.
  • 7肖文华,刘为纹.肝细胞癌RUNX3基因甲基化与杂合缺失的分析及其意义[J].中华肝脏病杂志,2004,12(4):227-230. 被引量:21
  • 8Park WS, Cho YG, Kim CA, et al. Hypermethylation of the RUNX3 gene in hepatocellular carcinoma [ J ]. Exp Mol Med,2005,37(4) :276 - 281.
  • 9Brueckner B, Kuck D, Lyko F.DNA methyltransferase inhibitors for cancer therapy [ J ]. Cancer Journal, 2007, 13 (1):17-22.
  • 10Brown KD, Robertson KD. DNMT1 knockout delivers a strong blow to genome stability and cell viability[J]. Nat Genet, 2007,39(3) :289 - 290.

二级参考文献27

  • 1李晓杰,谢海龙.肝细胞癌分子遗传学研究进展[J].湘南学院学报(医学版),2007,9(2):75-77. 被引量:2
  • 2Bangsow C, Rubins N, Glusman G, et al. The RUNX3 gene - sequence strcture and regulated expression [ J ]. Gene,2001,279 ( 2 ) ; 221 - 232.
  • 3LevanonD, Negreanu V, Bemsteim Y, et al. AML1, AML2, and AML3, the human members of the runt domain gene - family: cDNA structure, expression, and chromosomal localization [ J ]. Genomics,1994, 23(2) : 425 -432.
  • 4Bac SC, Choi JK. Tumor suppressor activity of RUNX3 [ J ]. Oncogene,2004, 23(24) :4336 -4340.
  • 5Ito Y. Molecular basis of tissur - specific gene expression mediated by the runt domain transcription factor PEBP2/CBF [ J ]. Gene Cells,1999,4(2) ; 685 -696.
  • 6Warren A J, Bravo J, WilliamsRL, et al. Structural basis for the heteredimeric interaction between the acute leukaem ia - associated transcription factorsAML1 and CBFbeta[J]. EMBO J, 2000, 19 (12) :3004 -3015.
  • 7Park W S, Cho YG, Kim C J, et al. Hypermethylation of the RUNX3 gene in hepatocellular carcinoma [ J ]. Exp Mol Med, 2005, 37(4) : 276 -281.
  • 8Simpson DJ, Hibberts NA, Mc Nicol AM, et al. Loss of pRb expression in pituitary adenomas is associated with methylation of the RB1 CpG island. Cancer Res, 2000, 60:1211-1216.
  • 9Fujimoto J, Yasui W, Tahara H, et al. DNA hypermethylation at the pS2 promoter region is associated with early stage of stomach carcinogenesis. Cancer Lett, 2000,149:125-134.
  • 10Lubomierski N, Kersting M, Bert T, et al. Tumor suppressor genes in the 9p21 gene cluster are selective targets of inactivation in neuroendocrine gastroenteropancreatic tumors. Cancer Res, 2001,61:5905-5910.

共引文献28

同被引文献10

引证文献1

二级引证文献1

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