PRC2
EZH2型
医学
临床试验
癌症
计算生物学
药理学
生物信息学
生物
组蛋白
内科学
遗传学
基因
作者
Millicent Dockerill,Clare Gregson,Daniel H. O’Donovan
标识
DOI:10.1080/13543776.2021.1841167
摘要
Introduction PRC2 is a histone methyltransferase complex associated with several cancer types. Tazemetostat was recently approved as the first inhibitor targeting the catalytic subunit EZH2 and several other EZH2 inhibitors are now under clinical evaluation. Beyond EZH2, researchers have also explored other approaches including PRC2 activators, dual agents inhibiting both EZH1 and EZH2, allosteric inhibitors binding to EED, and compounds which induce the degradation of PRC2 constituent proteins.Areas covered This review provides an overview of anticancer therapies targeting PRC2 during the period 2016–2020 including clinical trials, patents and the scientific literature.Expert opinion The approval of tazemetostat marks the clinical validation of EZH2 for the treatment of cancer. Despite this success many questions remain; for instance, tazemetostat was briefly placed on clinical hold for safety concerns, while another EZH2 inhibitor (GSK126) demonstrated insufficient efficacy during a Phase I/II trial. It is important to understand these risks as PRC2 therapies progress through clinic evaluation. Alternative approaches to target PRC2 may offer distinct advantages over the inhibition of EZH2, including the potential to overcome EZH2 resistance mutations. However, these emerging modalities may also incur new challenges as they progress toward the clinic. Nonetheless, the diversity of agents under development represents a wealth of therapeutic options for future patients.
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