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TM6SF2在肝细胞癌组织中的表达及其生物信息学功能分析

肖剑寒 刘守胜 赵真真 辛永宁 宣世英

引用本文:
Citation:

TM6SF2在肝细胞癌组织中的表达及其生物信息学功能分析

DOI: 10.3969/j.issn.1001-5256.2019.08.017
基金项目: 

国家自然科学基金面上项目(31770837); 

详细信息
  • 中图分类号: R735.7

Expression of TM6SF2 in hepatocellular carcinoma tissue and its bioinformatics functions

Research funding: 

 

  • 摘要:

    目的利用肿瘤数据库挖掘数据并分析TM6SF2在肝细胞癌(HCC)组织中的表达情况,同时探讨TM6SF2的生物学作用及功能。方法利用GEPIA数据库分析HCC组织中的TM6SF2基因mRNA水平的变化。利用OncoLnc做TM6SF2基因的表达水平与HCC患者生存期的相关性分析。利用cBioPortal数据库和LinkedOmics数据库分析TM6SF2在HCC组织中存在的表达相关基因。利用DAVID6. 8和STRING数据库对TM6SF2及其表达相关基因进行生物信息分析。用t检验验证HCC与癌旁组织基因mRNA表达差异。用Spearman相关系数分析基因表达的相关性。采用Kaplan-Meier生存分析计算生存率,采用广义log-rank检验估计生存率的差异。结果与正常肝组织相比,HCC组织中TM6SF2基因mRNA水平呈低表达(|log2FC|cut-off=0. 5,P <0. 01)。相比高表达的患者,TM6SF2低表达可明显降低HCC患者的总体生存时间(χ2=9. 897,P <0. 01)。数据分析显示,在HCC组织中与TM6SF2表达相关基因共49个。GO分析...

     

  • [1] BRAY F, FERLAY J, SOERJOMATARAM I, et al. Global cancer statistics 2018:GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J]. CA Cancer J Clin, 2018, 68 (6) :394-424.
    [2] LLOVET JM, ZUCMAN-ROSSI J, PIKARSKY E. Hepatocellular carcinoma[J]. Nat Rev Dis Primers, 2016, 2:16018.
    [3] LLOVET JM, MONTAL R, SIA D, et al. Molecular therapies and precision medicine for hepatocellular carcinoma[J]. Nat Rev Clin Oncol, 2018, 15 (10) :599-616.
    [4] MAHDESSIAN H, TAXIARCHIS A, POPOV S, et al. TM6SF2 is a regulator of liver fat metabolism influencing triglyceride secretion and hepatic lipid droplet content[J]. Proc Natl Acad Sci U S A, 2014, 111 (24) :8913-8918.
    [5] KOZLITINA J, SMAGRIS E, STENDER S, et al. Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease[J]. Nat Genet, 2014, 46 (4) :352-356.
    [6] CHALASANI N, WILSON L, KLEINER DE, et al. Relationship of steatosis grade and zonal location to histological features of steatohepatitis in adult patients with non-alcoholic fatty liver disease[J]. J Hepatol, 2008, 48 (5) :829-834.
    [7] KE RS, ZHANG K, LV LZ, Et al. Prognostic value and oncogene function of heterogeneous nuclear ribonucleoprotein A1overexpression in HBV-related hepatocellular carcinoma[J].Oncol Lett, 2018, 16 (3) :3746-3756.
    [8] ANAYA J. OncoLnc:Linking TCGA survival data to mRNAs, miRNAs, and lncRNAs[J]. Peer J Computer Science, 2016, 2:e67.
    [9] GAO J, AKSOY BA, DOGRUSOZ U, et al. Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal[J]. Sci Signal, 2013, 6 (269) :pl1.
    [10] VASAIKAR SV, STRAUB P, WANG J, et al. LinkedOmics:Analyzing multi-omics data within and across 32 cancer types[J]. Nucleic Acids Res, 2017, 46 (D1) :d956-d963.
    [11] HUANG DW, SHERMAN BT, LEMPICKI RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources[J]. Nat Protoc, 2009, 4 (1) :44-57.
    [12] SZKLARCZYK D, FRANCESCHINI A, WYDER S, et al. STRING v10:Protein-protein interaction networks, integrated over the tree of life[J]. Nucleic Acids Res, 2014, 43 (D1) :d447-d452.
    [13] ZHANG YP, WANG F, CHEN PF, et al. Expression and significance of the ABAT gene in hepatocellular carcinoma:An analysis based on data mining[J]. J Clin Hepatol, 2019, 35 (3) :553-558. (in Chinese) 张玉鹏, 王帆, 陈鹏飞, 等.基于数据挖掘分析ABAT基因在肝细胞癌中的表达及意义[J].临床肝胆病杂志, 2019, 35 (3) :553-558.
    [14] ESLAM M, GEORGE J. Genetic and epigenetic mechanisms of NASH[J]. Hepatol Int, 2016, 10 (3) :394-406.
    [15] ESLAM M, VALENTI L, ROMEO S. Genetics and epigenetics of NAFLD and NASH:Clinical impact[J]. J Hepatol, 2018, 68 (2) :268-279.
    [16] ROMEO S, KOZLITINA J, XING C, et al. Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease[J]. Nat Genet, 2008, 40 (12) :1461-1465.
    [17] DONGIOVANNI P, ROMEO S, VALENTI L. Genetic factors in the pathogenesis of nonalcoholic fatty liver and steatohepatitis[J]. Biomed Res Int, 2015, 2015:460190.
    [18] ANSTEE QM, SETH D, DAY CP. Genetic factors that affect risk of alcoholic and nonalcoholic fatty liver disease[J]. Gastroenterology, 2016, 150 (8) :1728-1744. e7.
    [19] FALLETI E, CUSSIGH A, CMET S, et al. PNPLA3 rs738409and TM6SF2 rs58542926 variants increase the risk of hepatocellular carcinoma in alcoholic cirrhosis[J]. Dig Liver Dis, 2016, 48 (1) :69-75.
    [20] RAKSAYOT M, CHUAYPEN N, KHLAIPHUENGSIN A, et al. Independent and additive effects of PNPLA3 and TM6SF2 polymorphisms on the development of non-B, non-C hepatocellular carcinoma[J]. J Gastroenterol, 2019, 54 (5) :427-436.
    [21] YANG J, TREPO E, NAHON P, et al. PNPLA3 and TM6SF2variants as risk factors of hepatocellular carcinoma across various etiologies and severity of underlying liver diseases[J]. Int J Cancer, 2019, 144 (3) :533-544.
    [22] MELLO T, MATEROZZI M, GALLI A. PPARs and mitochondrial metabolism:From NAFLD to HCC[J]. PPAR Res, 2016, 2016:7403230.
    [23] KIMURA O, KONDO Y, SHIMOSEGAWA T. PPAR could contribute to the pathogenesis of hepatocellular carcinoma[J].PPAR Res, 2012, 2012:574180.
    [24] DAI HH, MEI LQ. Advances in nonalcoholic fatty liver disease and hepatocellular carcinoma research[J]. J Clin Hepatol, 2012, 28 (10) :797-800. (in Chinese) 代鸿华, 梅礼强.非酒精性脂肪性肝病与肝细胞癌关系的研究进展[J].临床肝胆病杂志, 2012, 28 (10) :797-800.
    [25] DIEHL AM, DAY C. Cause, pathogenesis, and treatment of nonalcoholic steatohepatitis[J]. N Engl J Med, 2017, 377 (21) :2063-2072.
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  • 收稿日期:  2019-03-14
  • 出版日期:  2019-08-20
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