Hepatitis B viral load affects prognosis of hepatocellular carcinoma

被引:0
作者
Su Jong Yu [1 ]
Yoon Jun Kim [1 ]
机构
[1] Department of Internal Medicine and Liver Research Institute,Seoul National University College of Medicine,Seoul 110-744,South Korea
关键词
Hepatitis B virus; DNA; Hepatocellular carcinoma; Progression; Prognosis;
D O I
暂无
中图分类号
R735.7 [肝肿瘤];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma(HCC)is a complex disease that is dually challenging to treat due to underlying chronic liver disease in addition to the cancer itself.The prognosis of patients with HCC is determined by intrahepatic tumor status and reserved hepatic function.Hepatitis B virus(HBV)is an established major risk factor of HCC development,and HBV viral load is being increasingly recognized as a prognostic factor in the presence of established HCC.High HBV viral load may affect the prognosis of HBV-related HCC patients in several ways.First,it is associated with more frequent recurrence of HBV-related HCC after treatment.Second,it is associated with more occurrence and severity of potentially life-threatening HBV reactivation.Last,it is associated with more worsened liver function,which limits the therapeutic options for HBV-related HCC.HBV,directly or indirectly,can induce hepatocarcinogenesis.In patients with a high HBV DNA level and subsequent active hepatitis,adhesion molecules expressed on the sinusoidal cells are up-regulated and may increase intrahepatic metastasis.HCC progression after treatment can lead to a poor prognosis by reducing number of normal functioning hepatocytes.Thus,high HBV viral load can affect the prognosis of patientswith HCC by frequent recurrence after treatment for HCC and deterioration of hepatic function associated with HCC progression.Recent meta-analysis showed that antiviral treatment reduces HCC recurrence and liver-related mortality after curative therapy of HCC.Given the strong relationship between high HBV DNA load and poor survival outcome of HCC patients due to cancer progression,it is expected that long-term antiviral therapy results in the sustained HBV suppression,control of inflammation,reduction in HCC progression,and eventually in improved overall survival.
引用
收藏
页码:12039 / 12044
页数:6
相关论文
共 5 条
[2]   Survival factors after resection of small hepatocellular carcinoma [J].
Departments of Surgical Oncology Wu FS Zhao WH Ma ZM Teng LS and Wang M and General Surgery Liang TB and Zheng SS First Affiliated Hospital Zhejiang University School of Medicine Hangzhou China .
Hepatobiliary & Pancreatic Diseases International, 2005, (03) :379-384
[3]   Expression of heat shock proteins (HSP27, HSP60, HSP70, HSP90, GRP78, GRP94) in hepatitis B virus-related hepatocellular carcinomas and dysplastic nodules [J].
Seung Oe Lim ;
Sung Gyoo Park ;
Jun-Hi Yoo ;
Young Min Park ;
Hie-Joon Kim ;
Kee-Taek Jang ;
Jae Won Cho ;
Byung Chul Yoo ;
Gu-Hung Jung ;
Cheol Keun Park .
World Journal of Gastroenterology, 2005, (14) :2072-2079
[4]  
Tenofovir disoproxil fumarate (TDF), emtricitabine/TDF, and entecavir in patients with decompensated chronic hepatitis B liver disease[J] . Yun‐Fan Liaw,I‐Shyan Sheen,Chuan‐Mo Lee,Ulus Salih Akarca,George V. Papatheodoridis,Florence Suet‐Hing Wong,Ting‐Tsung Chang,Andrzej Horban,Chia Wang,Peter Kwan,Maria Buti,Martin Prieto,Thomas Berg,Kathryn Kitrinos,Ken Peschell,Elsa Mondou,David Frederick,Franck Rousseau,Eugene R. Schiff.Hepatology . 2011 (1)
[5]  
Glucose-regulated protein 78 is an intracellular antiviral factor against hepatitis B virus .2 Ma Yan,Yu Jun,Chan Henry L Y,Chen Yang-chao,Wang Hua,Chen Ying,Chan Chu-yan,Go Minnie Y Y,Tsai Sau-na,Ngai Sai-ming,To Ka-fai,Tong Joanna H M,He Qing-Yu,Sung Joseph J Y,Kung Hsiang-fu,Cheng Christopher H K,He Ming-liang. Molecular & cellular proteomics : MCP . 2009