Human papilloma virus, DNA methylation and microRNA expression in cervical cancer (Review)

被引:69
|
作者
Jimenez-Wences, Hilda [1 ]
Peralta-Zaragoza, Oscar [2 ]
Fernandez-Tilapa, Gloria [1 ]
机构
[1] Guerrero Autonomous Univ, Acad Unit Biol Chem Sci, Clin Res Lab, Chilpancingo 39070, Guerrero, Mexico
[2] Natl Inst Publ Hlth, Res Ctr Infect Dis, Direct Chron Infect & Canc, Cuernavaca 62100, Morelos, Mexico
关键词
miRNAs; methylation; human papilloma virus; cervical cancer; TUMOR-SUPPRESSOR MICRORNAS; CPG ISLAND HYPERMETHYLATION; EPIGENETIC REGULATION; MIRNA EXPRESSION; HPV INFECTION; GENE; HYPOMETHYLATION; METHYLTRANSFERASE-1; IDENTIFICATION; CONTRIBUTES;
D O I
10.3892/or.2014.3142
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer is a complex disease caused by genetic and epigenetic abnormalities that affect gene expression. The progression from precursor lesions to invasive cervical cancer is influenced by persistent human papilloma virus (HPV) infection, which induces changes in the host genome and epigenome. Epigenetic alterations, such as aberrant miRNA expression and changes in DNA methylation status, favor the expression of oncogenes and the silencing of tumor-suppressor genes. Given that some miRNA genes can be regulated through epigenetic mechanisms, it has been proposed that alterations in the methylation status of miRNA promoters could be the driving mechanism behind their aberrant expression in cervical cancer. For these reasons, we assessed the relationship among HPV infection, cellular DNA methylation and miRNA expression. We conclude that alterations in the methylation status of protein-coding genes and various miRNA genes are influenced by HPV infection, the viral genotype, the physical state of the viral DNA, and viral oncogenic risk. Furthermore, HPV induces deregulation of miRNA expression, particularly at loci near fragile sites. This deregulation occurs through the E6 and E7 proteins, which target miRNA transcription factors such as p53.
引用
收藏
页码:2467 / 2476
页数:10
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