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Advances of small molecule targeting of kinases

机译:小分子靶向激酶的研究进展

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摘要

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. ]]>
机译:<![cdata [ 可逆蛋白质磷酸化几乎调节了细胞中生命中的所有方面。结果,蛋白激酶的失调,其负责从ATP转移到蛋白质的磷酸盐基团的酶通常是许多人类疾病的原因或后果,包括癌症。自1995年以来,已经批准了近三次蛋白激酶抑制剂(PKIS),以便临床应用,绝大多数用于治疗癌症。根据NCI,有超过100种类型的癌症。但是,FDA批准的PKI只有其中14个。重要的是,由人类基因组编码的500多种蛋白激酶,仅为目前批准的PKIS的目标仅为22个,这表明PKI的储层仍然有很大增加的空间。在这次简短的审查中,我们将讨论最新的进展,挑战和替代本兴奋领域采用策略的替代品。 ]]>

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