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小分子靶向激酶的研究进展

Advances of small molecule targeting of kinases.

作者信息

Berndt Norbert, Karim Rezaul M, Schönbrunn Ernst

机构信息

Drug Discovery Department, Moffitt Cancer Center, 12902 Magnolia Drive, Tampa, FL 33612, USA.

Drug Discovery Department, Moffitt Cancer Center, 12902 Magnolia Drive, Tampa, FL 33612, USA.

出版信息

Curr Opin Chem Biol. 2017 Aug;39:126-132. doi: 10.1016/j.cbpa.2017.06.015. Epub 2017 Jul 18.

Abstract

Reversible protein phosphorylation regulates virtually all aspects of life in the cell. As a result, dysregulation of protein kinases, the enzymes responsible for transferring phosphate groups from ATP to proteins, are often the cause or consequence of many human diseases including cancer. Almost three dozen protein kinase inhibitors (PKIs) have been approved for clinical applications since 1995, the vast majority of them for the treatment of cancer. According to the NCI, there are more than 100 types of cancer. However, FDA-approved PKIs only target 14 of them. Importantly, of the more than 500 protein kinases encoded by the human genome, only 22 are targets for currently approved PKIs, suggesting that the reservoir of PKIs still has room to grow significantly. In this short review we will discuss the most recent advances, challenges, and alternatives to currently adopted strategies in this burgeoning field.

摘要

可逆性蛋白质磷酸化几乎调节着细胞生命活动的方方面面。因此,蛋白激酶(负责将磷酸基团从ATP转移至蛋白质的酶)功能失调往往是包括癌症在内的许多人类疾病的病因或结果。自1995年以来,近三十种蛋白激酶抑制剂(PKIs)已获批用于临床,其中绝大多数用于癌症治疗。据美国国家癌症研究所(NCI)称,癌症有100多种类型。然而,美国食品药品监督管理局(FDA)批准的PKIs仅针对其中14种。重要的是,人类基因组编码的500多种蛋白激酶中,目前仅有22种是获批PKIs的靶点,这表明PKIs储备仍有显著增长空间。在这篇简短的综述中,我们将探讨这一新兴领域中当前采用策略的最新进展、挑战及替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e9e/5728163/802f2eb0b6db/nihms894091f1.jpg

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