Sedeno-Monge Virginia, Vallejo-Ruiz Veronica, Sosa-Jurado Francisca, Santos-Lopez Gerardo
Departamento de Ciencias de la Salud, Universidad Popular Autonoma del Estado de Puebla, Puebla, Mexico.
J Biosci. 2017 Sep;42(3):509-521. doi: 10.1007/s12038-017-9695-4.
Little is known about the mechanisms underlying hepatocellular carcinoma (HCC). Some studies have focused on the role of HCV viral proteins in hepatocyte transformation. In this work we have compiled and analysed current articles regarding the impact of polymorphisms in the HCV core gene and protein on the development of HCC. An exhaustive search for fulltext articles until November 2016 in PubMed database was performed using the MeSH keywords: 'hepatitis C', 'polymorphisms', 'core', 'hepatocellular cancer' and 'hepatocarcinogenesis'. Nineteen full-text articles published between 2000 and 2016 were considered. Different articles associate not only the HCC development with polymorphisms at residues 70 and 91 in the core protein, but more with mortality and treatment response. Also, different polymorphisms were found in core and other viral proteins related to HCC development. Eleven articles reported that HCC development is significantly associated with Gln/His70, four associated it with Leu91 and two more associated it with both markers together. Additional studies are necessary, including those in different types of populations worldwide, to validate the possibility of the usability and influence in chronically HCV-infected patients as well as to observe their interaction with other risk factors or prognosis and genetic markers of the host.
关于肝细胞癌(HCC)的潜在机制,人们了解甚少。一些研究聚焦于丙型肝炎病毒(HCV)病毒蛋白在肝细胞转化中的作用。在这项工作中,我们收集并分析了当前有关HCV核心基因和蛋白多态性对HCC发生影响的文章。使用医学主题词(MeSH)关键词“丙型肝炎”“多态性”“核心”“肝细胞癌”和“肝癌发生”,在PubMed数据库中对截至2016年11月的全文文章进行了详尽检索。共纳入了2000年至2016年间发表的19篇全文文章。不同文章不仅将HCC的发生与核心蛋白70位和91位残基的多态性相关联,而且更多地与死亡率和治疗反应相关联。此外,在与HCC发生相关的核心蛋白及其他病毒蛋白中发现了不同的多态性。11篇文章报道HCC的发生与Gln/His70显著相关,4篇文章将其与Leu91相关联,另外2篇文章将其与这两个标记物均相关联。需要开展更多研究,包括针对全球不同人群的研究,以验证其在慢性HCV感染患者中的可用性和影响的可能性,并观察它们与其他危险因素或宿主的预后及遗传标记物之间的相互作用。