Targeting cancer metabolism in the era of precision oncology

癌症 免疫系统 癌细胞 癌症研究 细胞代谢 间质细胞 新陈代谢 肿瘤微环境 医学 生物 生物信息学 免疫学 内科学
作者
Zachary E. Stine,Zachary T. Schug,Joseph M. Salvino,Chi V. Dang
出处
期刊:Nature Reviews Drug Discovery [Springer Nature]
卷期号:21 (2): 141-162 被引量:557
标识
DOI:10.1038/s41573-021-00339-6
摘要

One hundred years have passed since Warburg discovered alterations in cancer metabolism, more than 70 years since Sidney Farber introduced anti-folates that transformed the treatment of childhood leukaemia, and 20 years since metabolism was linked to oncogenes. However, progress in targeting cancer metabolism therapeutically in the past decade has been limited. Only a few metabolism-based drugs for cancer have been successfully developed, some of which are in - or en route to - clinical trials. Strategies for targeting the intrinsic metabolism of cancer cells often did not account for the metabolism of non-cancer stromal and immune cells, which have pivotal roles in tumour progression and maintenance. By considering immune cell metabolism and the clinical manifestations of inborn errors of metabolism, it may be possible to isolate undesirable off-tumour, on-target effects of metabolic drugs during their development. Hence, the conceptual framework for drug design must consider the metabolic vulnerabilities of non-cancer cells in the tumour immune microenvironment, as well as those of cancer cells. In this Review, we cover the recent developments, notable milestones and setbacks in targeting cancer metabolism, and discuss the way forward for the field.
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