clinician for early urgent screening for HCC in cirrhotic patients [16]. Furthermore, under-expression of miR-122 was associated with poorer prognosis in HCC patients [17]. Similarly, histone modifying genes (EZH2 and SUV39HZ) and protein produced by phosphorylation of histone (ARK1 and ARK2) were all poor predictors of outcome and invasiveness [18] [19]. Recent study by Mansour et al. found that hypermethylation of RASSF1A positively correlated with increased tumor size but not with alpha-fetoprotein level and aggravate the hepatocarcinogenic process. The authors suggested the incorporation of RASSF1A measurement as a screening tool in patients at risk for HCC development [20]
All of those epigenetics biomarkers are promising target in HCC that provide clinicians better diagnostic and prognostic tool and in the future, epigenetic directed therapy might be developed.