肿瘤微环境
癌细胞
重编程
表观遗传学
癌症研究
癌症干细胞
药品
抗癌药
癌症
药理学
抗药性
生物
细胞
肿瘤细胞
生物化学
遗传学
基因
作者
Erica Pranzini,Elisa Pardella,Paolo Paoli,Sarah‐Maria Fendt,Maria Letizia Taddei
标识
DOI:10.1016/j.trecan.2021.02.004
摘要
Overcoming anticancer drug resistance is a major challenge in cancer therapy, requiring innovative strategies that consider the extensive tumor heterogeneity and adaptability. We provide recent evidence highlighting the key role of amino acid (AA) metabolic reprogramming in cancer cells and the supportive microenvironment in driving resistance to anticancer therapies. AAs sustain the acquisition of anticancer resistance by providing essential building blocks for biosynthetic pathways and for maintaining a balanced redox status, and modulating the epigenetic profile of both malignant and non-malignant cells. In addition, AAs support the reduced intrinsic susceptibility of cancer stem cells to antineoplastic therapies. These findings shed new light on the possibility of targeting nonresponding tumors by modulating AA availability through pharmacological or dietary interventions.
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