Treatment for Viral Hepatitis as Secondary Prevention for Hepatocellular Carcinoma

被引:18
作者
Alqahtani, Saleh A. [1 ,2 ,3 ]
Colombo, Massimo [4 ]
机构
[1] Johns Hopkins Univ, Div Gastroenterol & Hepatol, Baltimore, MD 21287 USA
[2] King Faisal Specialist Hosp & Res Ctr, Liver Transplant Ctr, Riyadh 11564, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Biostat Epidemiol & Sci Comp Dept, Riyadh 11564, Saudi Arabia
[4] IRCCS San Raffaele Hosp, Liver Ctr, I-20132 Milan, Italy
关键词
HCC; HBC; HCV; hepatocellular carcinoma; prevention; B-VIRUS INFECTION; TENOFOVIR DISOPROXIL FUMARATE; ACTING ANTIVIRAL THERAPY; C VIRUS; LIVER-CANCER; X-PROTEIN; HBSAG SEROCLEARANCE; INTERFERON THERAPY; SCORING SYSTEM; RISK SCORE;
D O I
10.3390/cells10113091
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chronic infections with either hepatitis B or C virus (HBV or HCV) are among the most common risk factors for developing hepatocellular carcinoma (HCC). The hepatocarcinogenic potential of these viruses is mediated through a wide range of mechanisms, including the induction of chronic inflammation and oxidative stress and the deregulation of cellular pathways by viral proteins. Over the last decade, effective anti-viral agents have made sustained viral suppression or cure a feasible treatment objective for most chronic HBV/HCV patients. Given the tumorigenic potential of HBV/HCV, it is no surprise that obtaining sustained viral suppression or eradication proves to be effective in preventing HCC. This review summarizes the mechanisms by which HCV and HBV exert their hepatocarcinogenic activity and describes in detail the efficacy of anti-HBV and anti-HCV therapies in terms of HCC prevention. Although these treatments significantly reduce the risk for HCC in patients with chronic viral hepatitis, this risk is not eliminated. Therefore, we evaluate potential strategies to improve these outcomes further and address some of the remaining controversies.
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页数:20
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