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乙肝病毒感染土拨鼠模型中的肝细胞癌

Hepatocellular carcinoma in the woodchuck model of hepatitis B virus infection.

作者信息

Tennant Bud C, Toshkov Ilia A, Peek Simon F, Jacob James R, Menne Stephan, Hornbuckle William E, Schinazi Raymond D, Korba Brent E, Cote Paul J, Gerin John L

机构信息

Gastrointestinal Unit, Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14953, USA.

出版信息

Gastroenterology. 2004 Nov;127(5 Suppl 1):S283-93. doi: 10.1053/j.gastro.2004.09.043.

Abstract

The Eastern woodchuck ( Marmota monax ) harbors a DNA virus (Woodchuck hepatitis virus [WHV]) that is similar in structure and replicative life cycle to the human hepatitis B virus (HBV). Like HBV, WHV infects the liver and can cause acute and chronic hepatitis. Furthermore, chronic WHV infection in woodchucks usually leads to development of hepatocellular carcinoma (HCC) within the first 2-4 years of life. The woodchuck model has been important in the preclinical evaluation of safety and efficacy of the antiviral drugs now in use for treatment of HBV infection and continues to serve as an important, predictive model for innovative forms of therapy of hepatitis B using antiviral nucleosides and immune response modifiers alone or in combination. Almost all woodchucks that become chronic WHV carriers after experimental neonatal inoculation develop HCC with a median HCC-free survival of 24 months and a median life expectancy of 30-32 months. The woodchuck model of viral-induced HCC has been used effectively for the development of new imaging agents for enhancement of detection of hepatic neoplasms by ultrasound and magnetic resonance imaging. The chemoprevention of HCC using long-term antiviral nucleoside therapy has been shown in the woodchuck, and "proof of principal" has been established for some of the innovative, molecular methods for treatment of HCC. The model is available for fundamental investigations of the viral and molecular mechanisms responsible for hepatocarcinogenesis and should have substantial value for future development of innovative methods for chemoprevention and gene therapy of human HCC.

摘要

东部土拨鼠(Marmota monax)携带一种DNA病毒(土拨鼠肝炎病毒[WHV]),其结构和复制生命周期与人类乙型肝炎病毒(HBV)相似。与HBV一样,WHV感染肝脏,可引起急性和慢性肝炎。此外,土拨鼠慢性感染WHV通常会在其生命的头2至4年内发展为肝细胞癌(HCC)。土拨鼠模型在目前用于治疗HBV感染的抗病毒药物的临床前安全性和有效性评估中具有重要意义,并继续作为使用抗病毒核苷和免疫反应调节剂单独或联合治疗乙型肝炎的创新疗法的重要预测模型。几乎所有在实验性新生儿接种后成为慢性WHV携带者的土拨鼠都会发展为HCC,无HCC存活的中位数为24个月,平均预期寿命为30至32个月。病毒诱导的HCC土拨鼠模型已有效地用于开发新的成像剂,以增强超声和磁共振成像对肝脏肿瘤的检测。土拨鼠模型已证明长期使用抗病毒核苷疗法可化学预防HCC,并且已为一些治疗HCC的创新分子方法建立了“原理证明”。该模型可用于对导致肝癌发生的病毒和分子机制进行基础研究,并且对人类HCC化学预防和基因治疗创新方法的未来发展应具有重要价值。

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