细胞信号传导中的蛋白激酶C:开发选择性抑制剂的策略。

P M Blumberg, G Acs, P Acs, L B Areces, M G Kazanietz, N E Lewin, Z Szallasi
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引用次数: 11

摘要

蛋白激酶C在亲脂性第二信使sn-1,2-二酰基甘油的细胞信号通路中起核心作用,参与许多生物反应,包括肿瘤促进和炎症。为了制定选择性抑制的策略,一项主要的工作是了解该系统内的多样性。已经确定了蛋白激酶C调节区域的两类配体,尽管它们在体外作为酶的激活剂起作用,但在体内却矛盾地表现为部分拮抗剂。对不同于蛋白激酶C的磷酸酯的靶标的鉴定表明,作用于蛋白激酶C的调节和催化结构域的拮抗剂将具有不同的作用谱。
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Protein kinase C in cell signaling: strategies for the development of selective inhibitors.

Protein kinase C plays a central role in the cellular signaling pathway for the lipophilic second messenger sn-1,2-diacylglycerol, which is involved in many biological responses, including tumor promotion and inflammation. A major effort has been directed at understanding diversity within this system in order to develop strategies for selective inhibition. Two classes of ligands for the regulatory domain of protein kinase C have been identified which, although they function in vitro as activators of the enzyme, paradoxically behave in vivo as partial antagonists. Identification of targets for the phorbol esters distinct from protein kinase C argues that antagonists acting on the regulatory and catalytic domains of protein kinase C will have different spectra of action.

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