药品
药理学
对偶(语法数字)
药物开发
抗药性
透视图(图形)
药物发现
医学
计算生物学
生物信息学
计算机科学
生物
遗传学
人工智能
文学类
艺术
作者
Philip E. Thompson,Jake Shortt
标识
DOI:10.1016/j.tips.2024.04.008
摘要
Members of the MYC family of proteins are a major target for cancer drug discovery, but the development of drugs that block MYC-driven cancers has not yet been successful. Approaches to achieve success may include the development of combination therapies or dual-acting drugs that target MYC at multiple nodes. Such treatments hold the possibility of additive or synergistic activity, potentially reducing side effect profiles and the emergence of resistance. In this review, we examine the prominent MYC-related targets and highlight those that have been targeted in combination and/or dual-target approaches. Finally, we explore the challenges of combination and dual-target approaches from a drug development perspective.
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