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A model of interaction: Aflatoxins and hepatitis viruses in liver cancer aetiology and prevention

机译:一种相互作用模型:肝癌的肝毒素和肝炎病毒缓解学和预防

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Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide and has an extremely poor prognosis. The majority of cases occur in south-east Asia and sub-Saharan Africa where the major risk factors are chronic infection with hepatitis B and C viruses (HBV and HCV) as well as dietary exposure to aflatoxins. Aflatoxin B1, the most commonly occurring and potent of the aflatoxins is associated with a specific AGG to AGT transversion mutation at codon 249 of the p53 gene in human HCC, providing mechanistic support to a causal link between exposure and disease. Prospective epidemiological studies have shown a more than multiplicative interaction between HBV and aflatoxins in terms of HCC risk. However, the biology underlying this statistical interaction is not fully understood. There are a number of potential mechanisms including, among others: the fixation of AFB1-induced mutations in the presence of liver regeneration and hyperplasia induced by chronic HBV infection; the predisposition of HBV-infected hepatocytes to aflatoxin-induced DNA damage; an increase in susceptibility to chronic HBV infection in aflatoxin-exposed individuals; and oxidative stress exacerbated by co-exposure to aflatoxins and chronic hepatitis infection. Priorities for prevention are global HBV vaccination, primary and secondary prevention strategies against aflatoxin and the avoidance of transmission of HCV through good hygiene practices.
机译:肝细胞癌(HCC)是全世界最常见的癌症之一,预后极差。大多数病例发生在东南亚和撒哈拉以南非洲,其中主要危险因素是乙型肝炎和C病毒(HBV和HCV)的慢性感染以及饮食暴露于黄曲霉毒素。黄曲霉毒素B1,最常见的Aglatoxins的有效性与人HCC中P53基因的密码子249的特异性AgG至AgT转化突变有关,为暴露和疾病之间的因果关系提供机械支持。前瞻性流行病学研究显示了HBV和黄曲霉毒素在HCC风险方面的繁殖相互作用。然而,这种统计互动的生物学尚未完全理解。存在许多潜在的机制,包括:在慢性HBV感染诱导的肝再生和增生中固定AFB1诱导的突变; HBV感染的肝细胞倾向于黄曲霉毒素诱导的DNA损伤;黄曲霉毒素暴露个体慢性HBV感染易感性增加;通过共同暴露于黄曲霉毒素和慢性肝炎感染而加剧了氧化应激。预防优先事项是全球HBV疫苗接种,初级和二级预防策略对黄曲霉毒素以及通过良好的卫生实践避免HCV传播。

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