pi3激酶抑制:药物开发的靶点?

Robert C. Stein PhD, MRCP (Clinical Scientist and Senior Lecturer in Oncology) , Michael D. Waterfield FRS (Director of Research and Head of Department)
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引用次数: 207

摘要

磷酸肌肽3-激酶(pi3 -激酶)是一个普遍表达的酶家族,通过产生磷脂第二信使,在许多细胞过程的调节中发挥关键作用。这些包括运动、增殖和存活,以及碳水化合物代谢。本文综述了pi3激酶家族成员及其相关激酶、它们的激活机制和它们影响的细胞事件。随着对其参与疾病过程的认识的增加,pi3激酶似乎越来越成为药物开发的一个有吸引力的靶标,特别是在癌症和其他增殖性疾病领域,以及炎症和免疫疾病的治疗方面。pi3激酶同种异构体功能特化的证据表明,具有可接受毒性的选择性抑制可能是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PI3-kinase inhibition: a target for drug development?

The phosphoinositide 3-kinases (PI3-kinases) are a ubiquitously expressed enzyme family that, through the generation of phospholipid second messengers, play a key role in the regulation of many cellular processes. These include motility, proliferation and survival, and carbohydrate metabolism. Members of the PI3-kinase family and related kinases, their mechanism of activation and the cellular events that they influence are described in this review. As knowledge of their involvement in disease processes increases, the PI3-kinases appear to be an increasingly attractive target for drug development, particularly in the fields of cancer and other proliferative diseases, and in the treatment of inflammatory and immunological conditions. Evidence of the functional specialization of PI3-kinase isoforms suggests that selective inhibition with acceptable toxicity might be possible.

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