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直接小分子 AMPK 激活剂的前景与挑战。

Promise and challenges for direct small molecule AMPK activators.

机构信息

INSERM, U1016, Institut Cochin, Paris, France; CNRS, UMR8104, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, France.

INSERM, U1016, Institut Cochin, Paris, France; CNRS, UMR8104, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, France.

出版信息

Biochem Pharmacol. 2018 Jul;153:147-158. doi: 10.1016/j.bcp.2018.01.049. Epub 2018 Feb 3.

Abstract

AMP-activated protein kinase (AMPK) is an evolutionary conserved and ubiquitously expressed serine/threonine kinase playing a central role in the coordination of energy homeostasis. Based on the beneficial outcomes of its activation on metabolism, AMPK has emerged as an attractive target for the treatment of metabolic diseases. Identification of novel downstream targets of AMPK beyond the regulation of energy metabolism has renewed considerable attention in exploiting AMPK signaling for novel therapeutic targeting strategies including treatment of cancer and inflammatory diseases. The complexity of AMPK system with tissue- and species-specific expression of multiple isoform combination regulated by various inputs, post-traductional modifications and subcellular locations presents unique challenges for drug discovery. Here, we review the most recent advances in the understanding of the mechanism(s) of action of direct small molecule AMPK activators and the potential therapeutic opportunities.

摘要

腺苷酸活化蛋白激酶 (AMPK) 是一种进化上保守且广泛表达的丝氨酸/苏氨酸激酶,在能量代谢的协调中起着核心作用。基于其对代谢的激活所带来的益处,AMPK 已成为治疗代谢性疾病的一个有吸引力的靶点。除了对能量代谢的调节之外,AMPK 的新下游靶点的鉴定重新引起了人们对利用 AMPK 信号转导的关注,包括癌症和炎症性疾病的治疗。AMPK 系统的复杂性在于多种同工型组合的组织和物种特异性表达,受多种输入、翻译后修饰和亚细胞定位的调节,这给药物发现带来了独特的挑战。在这里,我们综述了直接小分子 AMPK 激活剂作用机制的最新进展及其潜在的治疗机会。

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