Epigenetic mechanisms regulating the development of hepatocellular carcinoma and their promise for therapeutics

被引:49
作者
Khan, Faisal Saeed [1 ]
Ali, Ijaz [2 ]
Afridi, Ume Kalsoom [3 ]
Ishtiaq, Muhammad [4 ]
Mehmood, Rashid [5 ]
机构
[1] Royal Hobart Hosp Tasmania, Hobart, Tas, Australia
[2] COMSATS Inst Informat Technol, Islamabad, Pakistan
[3] Abdul Wali Khan Univ Mardan, Dept Biochem, Mardan 25200, Pakistan
[4] Western Univ, London, ON, Canada
[5] Western Univ, London Hlth Sci Ctr, Childrens Hlth Res Inst, Victoria Res Labs, 800 Commissioners Rd E, London, ON, Canada
关键词
Hepatocarcinogenesis; HCC; Epigenetic regulation; Therapeutics; Epi-drugs; Tumor suppressors; TUMOR-SUPPRESSOR GENE; HISTONE DEACETYLASE INHIBITORS; GENOME-WIDE ANALYSIS; HUMAN LIVER-CANCER; DOWN-REGULATION; HEPATOMA-CELLS; HIGH-FREQUENCY; HEPATITIS-B; CPG ISLAND; PROMOTER HYPERMETHYLATION;
D O I
10.1007/s12072-016-9743-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatocellular carcinoma (HCC) is one of the most common cancers around the globe and third most fatal malignancy. Chronic liver disorders such as chronic hepatitis and liver cirrhosis often lead to the development of HCC. Accumulation of genetic and epigenetic alterations are involved in the development of HCC. Genetic research sparked by recent developments in next generation sequencing has identified the frequency of genetic alterations that occur in HCC and has led to the identification of genetic hotspots. Emerging evidence suggests that epigenetic aberrations are strongly associated with the initiation and development of HCC. Various important genes encoding tumor suppressors including P16, RASSF1A, DLC-1, RUNX3 and SOCS-1 are targets of epigenetic dysregulation during the development of HCC. The present review discusses the importance of epigenetic regulations including DNA methylation, histone modification and microRNA mediated regulation of gene expression during tumorigenesis and their use as disease biomarkers. Furthermore, these epigenetic alterations have been discussed in relationship with promising therapeutic perspectives for HCC and related cancers.
引用
收藏
页码:45 / 53
页数:9
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