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通过药物化学的视角看合成致死性。

Synthetic Lethality through the Lens of Medicinal Chemistry.

机构信息

Computational & Chemical Biology, Istituto Italiano di Tecnologia, 16163 Genova, Italy.

Department of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.

出版信息

J Med Chem. 2020 Dec 10;63(23):14151-14183. doi: 10.1021/acs.jmedchem.0c00766. Epub 2020 Nov 2.

Abstract

Personalized medicine and therapies represent the goal of modern medicine, as drug discovery strives to move away from one-cure-for-all and makes use of the various targets and biomarkers within differing disease areas. This approach, especially in oncology, is often undermined when the cells make use of alternative survival pathways. As such, acquired resistance is unfortunately common. In order to combat this phenomenon, synthetic lethality is being investigated, making use of existing genetic fragilities within the cancer cell. This Perspective highlights exciting targets within synthetic lethality, (PARP, ATR, ATM, DNA-PKcs, WEE1, CDK12, RAD51, RAD52, and PD-1) and discusses the medicinal chemistry programs being used to interrogate them, the challenges these programs face, and what the future holds for this promising field.

摘要

个性化医学和疗法代表了现代医学的目标,因为药物发现力求避免“一刀切”的方法,而是利用不同疾病领域中的各种靶点和生物标志物。在肿瘤学中,当细胞利用替代生存途径时,这种方法经常受到阻碍。因此,获得性耐药是很常见的。为了应对这种现象,正在研究合成致死性,利用癌细胞中现有的遗传脆弱性。本观点重点介绍了合成致死性中的令人兴奋的靶点(PARP、ATR、ATM、DNA-PKcs、WEE1、CDK12、RAD51、RAD52 和 PD-1),并讨论了用于研究这些靶点的药物化学方案、这些方案面临的挑战以及这个有前途的领域的未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/8015234/3915a2582443/jm0c00766_0001.jpg

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