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Integrative Analysis of DNA Methylation and microRNA Expression Reveals Mechanisms of Racial Heterogeneity in Hepatocellular Carcinoma.DNA甲基化与微小RNA表达的综合分析揭示肝细胞癌种族异质性的机制
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3
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1
Reduced expression of microRNA-139-5p in hepatocellular carcinoma results in a poor outcome: An exploration the roles of microRNA-139-5p in tumorigenesis, advancement and prognosis at the molecular biological level using an integrated meta-analysis and bioinformatic investigation.肝细胞癌中微小RNA-139-5p表达降低导致预后不良:一项使用综合荟萃分析和生物信息学研究在分子生物学水平上探索微小RNA-139-5p在肿瘤发生、进展和预后中的作用的研究。
Oncol Lett. 2019 Dec;18(6):6704-6724. doi: 10.3892/ol.2019.11031. Epub 2019 Nov 1.
2
LncRNA AFAP1-AS1 Supresses miR-139-5p and Promotes Cell Proliferation and Chemotherapy Resistance of Non-small Cell Lung Cancer by Competitively Upregulating RRM2.长链非编码RNA AFAP1-AS1通过竞争性上调RRM2抑制miR-139-5p并促进非小细胞肺癌的细胞增殖和化疗耐药性。
Front Oncol. 2019 Oct 22;9:1103. doi: 10.3389/fonc.2019.01103. eCollection 2019.
3
An integrated analysis of genome-wide DNA methylation and gene expression data in hepatocellular carcinoma.肝细胞癌全基因组DNA甲基化与基因表达数据的综合分析
FEBS Open Bio. 2018 May 30;8(7):1093-1103. doi: 10.1002/2211-5463.12433. eCollection 2018 Jul.
4
MiR-93-5p Promotes Cell Proliferation through Down-Regulating PPARGC1A in Hepatocellular Carcinoma Cells by Bioinformatics Analysis and Experimental Verification.通过生物信息学分析和实验验证,miR-93-5p通过下调肝细胞癌细胞中的PPARGC1A促进细胞增殖
Genes (Basel). 2018 Jan 22;9(1):51. doi: 10.3390/genes9010051.
5
miR-139-5p inhibits aerobic glycolysis, cell proliferation, migration, and invasion in hepatocellular carcinoma via a reciprocal regulatory interaction with ETS1.miR-139-5p 通过与 ETS1 的相互调节作用抑制肝癌细胞的有氧糖酵解、增殖、迁移和侵袭。
Oncogene. 2018 Mar;37(12):1624-1636. doi: 10.1038/s41388-017-0057-3. Epub 2018 Jan 16.
6
The identification of key genes and pathways in hepatocellular carcinoma by bioinformatics analysis of high-throughput data.通过高通量数据的生物信息学分析鉴定肝细胞癌中的关键基因和信号通路。
Med Oncol. 2017 Jun;34(6):101. doi: 10.1007/s12032-017-0963-9. Epub 2017 Apr 21.
7
Epigenetic basis of cancer health disparities: Looking beyond genetic differences.癌症健康差异的表观遗传学基础:超越遗传差异。
Biochim Biophys Acta Rev Cancer. 2017 Aug;1868(1):16-28. doi: 10.1016/j.bbcan.2017.01.001. Epub 2017 Jan 17.
8
DNA methylation contributes to deregulation of 12 cancer-associated microRNAs and breast cancer progression.DNA甲基化导致12种癌症相关微小RNA的失调及乳腺癌进展。
Gene. 2017 Mar 10;604:1-8. doi: 10.1016/j.gene.2016.12.018. Epub 2016 Dec 18.
9
Meta-analysis of DNA methylation biomarkers in hepatocellular carcinoma.肝细胞癌中DNA甲基化生物标志物的Meta分析。
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Differential Expression of MicroRNAs in Hepatitis C Virus-Mediated Liver Disease Between African Americans and Caucasians: Implications for Racial Health Disparities.非裔美国人和高加索人丙型肝炎病毒介导的肝病中微小RNA的差异表达:对种族健康差异的影响
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与肝细胞癌差异机制相关的表观遗传变化。

Epigenetic changes associated with mechanisms of disparities in hepatocellular carcinoma.

作者信息

Varghese Rency S, Zhou Yuan, Chen Yifan, Barefoot Megan E, Tadesse Mahlet, Ressom Habtom W

出版信息

Annu Int Conf IEEE Eng Med Biol Soc. 2020 Jul;2020:5320-5325. doi: 10.1109/EMBC44109.2020.9176036.

DOI:10.1109/EMBC44109.2020.9176036
PMID:33019185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9576401/
Abstract

In addition to socioeconomic influences, biological factors are believed to play a role in health disparities. In this paper, we investigate miRNA, mRNA, and DNA methylation patterns that contribute to disparities in hepatocellular carcinoma (HCC). This is accomplished by integration of mRNA-Seq, miRNA-Seq, and DNA methylation data we acquired by analysis of liver tissues from 30 HCC patients consisting of European Americans (EAs), African Americans (AAs), and Asian Americans (Asians). Mixed-ANOVA models are applied to identify miRNAs, mRNAs, and DNA methylation sites that are significantly altered in tumor vs. adjacent normal tissues in a race-specific manner. Through integrated analysis, a refined list of differentially expressed mRNAs is obtained by selecting those that are targets of differentially expressed miRNAs and consist of promoter regions that are differentially methylated.

摘要

除社会经济影响外,生物因素也被认为在健康差异中起作用。在本文中,我们研究了导致肝细胞癌(HCC)差异的微小RNA(miRNA)、信使核糖核酸(mRNA)和DNA甲基化模式。这是通过整合我们对30例HCC患者肝脏组织分析获得的mRNA测序、miRNA测序和DNA甲基化数据来实现的,这些患者包括欧裔美国人(EA)、非裔美国人(AA)和亚裔美国人(Asian)。应用混合方差分析模型,以种族特异性方式识别在肿瘤组织与相邻正常组织中显著改变的miRNA、mRNA和DNA甲基化位点。通过综合分析,通过选择那些是差异表达miRNA的靶标且包含差异甲基化启动子区域的mRNA,获得了一份经过细化的差异表达mRNA列表。