针对 Menin-KMT2A 相互作用的治疗方法

Pablo R. Freire, Jevon A. Cutler, Scott A. Armstrong
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摘要

直接靶向染色质相关蛋白越来越被认为是一种潜在的癌症治疗策略。在本综述中,我们将讨论一个突出的例子,即针对menin-KMT2A相互作用的小分子抑制剂。这些分子目前正在临床试验中进行研究,并显示出巨大的前景。我们描述了 Menin-KMT2A 蛋白复合物对一小部分基因转录调控的独特特异性,这些基因驱动着发育和白血病基因的表达。我们回顾了染色质相关的 KMT2A 复合物以及 menin 和 KMT2A 之间的蛋白相互作用,这种相互作用对于不同类型的癌细胞(最显著的是急性髓性白血病(AML))的维持至关重要。我们还总结了 menin 抑制剂的发展及其对染色质的影响。最后,我们讨论了在急性髓性白血病患者中进行的临床试验所取得的令人鼓舞的早期结果,以及最近发现的耐药menin突变体,这些突变体验证了menin是一个治疗靶点,但也可能带来治疗上的挑战。《癌症生物学年度综述》第8卷的最终在线出版日期预计为2024年4月。修订后的预计日期请参见 http://www.annualreviews.org/page/journal/pubdates。
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Therapeutic Targeting of the Menin–KMT2A Interaction
The direct targeting of chromatin-associated proteins is increasingly recognized as a potential therapeutic strategy for the treatment of cancer. In this review, we discuss a prominent example, namely, small-molecule inhibitors that target the menin–KMT2A interaction. These molecules are currently being investigated in clinical trials and showing significant promise. We describe the unique specificity of menin–KMT2A protein complexes for the transcriptional regulation of a small subset of genes that drive developmental and leukemic gene expression. We review the chromatin-associated KMT2A complex and the protein–protein interaction between menin and KMT2A that is essential for the maintenance of different types of cancer cells, but most notably acute myeloid leukemia (AML). We also summarize the development of menin inhibitors and their effects on chromatin. Finally, we discuss the promising early results from clinical trials in patients with AML and the recent discovery of therapy-resistant menin mutants that validate menin as a therapeutic target but also may present therapeutic challenges.Expected final online publication date for the Annual Review of Cancer Biology, Volume 8 is April 2024. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
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