...
首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Candidate genes responsible for human hepatocellular carcinoma identified from differentially expressed genes in hepatocarcinogenesis of the tree shrew (Tupaia belangeri chinesis).
【24h】

Candidate genes responsible for human hepatocellular carcinoma identified from differentially expressed genes in hepatocarcinogenesis of the tree shrew (Tupaia belangeri chinesis).

机译:从树sh的肝癌发生中差异表达的基因中鉴定出负责人类肝细胞癌的候选基因(Tupaia belangeri chinesis)。

获取原文
获取原文并翻译 | 示例
           

摘要

Aim: To explore gene expression profiles during hepatocarcinogenesis of the tree shrew, and to find the genes responsible for human hepatocellular carcinoma (HCC). Methods: Tree shrews were used as an animal model for HCC induction employing aflatoxin B(1) (AFB(1)) alone or AFB(1) plus hepatitis B virus (HBV) as etiological factors. Gene expression profiles from the tissues of HCC, HCC-surrounding liver tissues (para-HCC) and the corresponding biopsies taken from the same animals before HCC had developed (pre-HCC) were analyzed by cDNA microarray assay to identify differentially expressed genes. Two genes, CuZn-superoxide dismutase (SOD1) and glutathione S-transferase A1 (GSTA1), were further investigated by reverse transcriptase-polymerase chain reaction (RT-PCR) and immunohistochemical (IHC) assays were done on tree shrew and human HCC samples. Results: Results from the cDNA microarray analysis indicated that the gene expression profiles of HCC between AFB(1)and AFB(1) + HBV treatment groups were markedly different. A total of 11 genes, including SOD1 and GSTA1, were found changing in expression levels in all detected samples from both groups. Results from RT-PCR and IHC assays indicated that mRNA and protein levels of SOD1 and GSTA1 were markedly downregulated in both tree shrew and human HCC, and downregulation of SOD1 and GSTA1 proteins in human HCC samples was closely correlated with the histopathological grading (P < 0.05). Conclusion: The differentially expressed genes found in all HCC cases induced by different etiological factors among different species should be considered as good candidate genes responsible for HCC. Downregulation of SOD1 and GSTA1 might play an important role in hepatocarcinogenesis.
机译:目的:探讨树sh肝癌发生过程中的基因表达谱,并寻找引起人类肝细胞癌(HCC)的基因。方法:将树sh用作单独使用黄曲霉毒素B(1)(AFB(1))或AFB(1)加乙型肝炎病毒(HBV)作为病因的HCC诱导动物模型。通过cDNA微阵列分析法分析了来自肝癌组织,肝癌周围肝组织(对肝癌)和从肝癌发生前(相同肝癌)取自同一动物的相应活检组织的基因表达谱,以鉴定差异表达的基因。通过逆转录聚合酶链反应(RT-PCR)进一步研究了CuZn超氧化物歧化酶(SOD1)和谷胱甘肽S-转移酶A1(GSTA1)两个基因,并在树sh和人类HCC样品上进行了免疫组化(IHC)分析。结果:cDNA芯片分析结果表明,AFB(1)和AFB(1)+ HBV治疗组之间的肝癌基因表达谱有显着差异。在两组中所有检测到的样品中,共发现11个基因,包括SOD1和GSTA1,其表达水平发生了变化。 RT-PCR和IHC分析的结果表明,树sh和人HCC中SOD1和GSTA1的mRNA和蛋白水平均显着下调,人HCC样品中SOD1和GSTA1蛋白的下调与组织病理学分级密切相关(P < 0.05)。结论:在不同物种中,由不同病因引起的所有HCC病例中发现的差异表达基因应被认为是负责HCC的良好候选基因。 SOD1和GSTA1的下调可能在肝癌发生中起重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号