Alonso-Peña Marta, Sanchez-Martin Anabel, Sanchon-Sanchez Paula, Soto-Muñiz Meraris, Espinosa-Escudero Ricardo, Marin Jose J G
Experimental Hepatology and Drug Targeting (HEVEFARM), IBSAL, University of Salamanca, Salamanca 37007, Spain.
Center for the Study of Liver and Gastrointestinal Diseases (CIBERehd). Carlos III National Institute of Health, Madrid 28029, Spain.
Cancer Drug Resist. 2019 Sep 19;2(3):680-709. doi: 10.20517/cdr.2019.006. eCollection 2019.
Primary liver cancers constitute the fourth most deadly group of cancers. Their poor prognosis is due in part to the pre-existence and/or development, often during treatment, of powerful mechanisms accounting for the poor response of cancer cells to antitumor drugs. These include both impaired gene expression and the appearance of spliced variants, polymorphisms and mutations, affecting the function of genes leading to the reduction in intracellular concentrations of active agents, changes in molecular targets and survival pathways, altered tumor microenvironment and phenotypic transition. The present review summarizes available information regarding the role of germline and somatic mutations affecting drug transporters, enzymes involved in drug metabolism, organelles and signaling molecules related to liver cancer chemoresistance. A more complete picture of the actual complexity of this problem is urgently needed for carrying out further pharmacogenomic studies aimed to improve the management of patients suffering from hepatocellular carcinoma or cholangiocarcinoma.
原发性肝癌是第四大致命癌症类型。其预后较差,部分原因是在治疗期间,常常存在强大的机制,这些机制导致癌细胞对抗肿瘤药物反应不佳。这些机制包括基因表达受损以及剪接变体、多态性和突变的出现,这些会影响基因功能,导致细胞内活性剂浓度降低、分子靶点和生存途径发生变化、肿瘤微环境改变以及表型转变。本综述总结了有关种系和体细胞突变在肝癌化疗耐药中作用的现有信息,这些突变影响药物转运蛋白、参与药物代谢的酶、细胞器和信号分子。迫切需要更全面地了解这一问题的实际复杂性,以便开展进一步的药物基因组学研究,改善肝细胞癌或胆管癌患者的治疗管理。