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丝裂原活化蛋白激酶(MAPK)和生存 PI3K/Akt 通路之间的串扰:微妙的平衡。

Cross-talk between mitogenic Ras/MAPK and survival PI3K/Akt pathways: a fine balance.

机构信息

Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, 1020 Locust Street, Philadelphia, PA 19107, USA.

出版信息

Biochem Soc Trans. 2012 Feb;40(1):139-46. doi: 10.1042/BST20110609.

Abstract

In the present paper, we describe multiple levels of cross-talk between the PI3K (phosphoinositide 3-kinase)/Akt and Ras/MAPK (mitogen-activated protein kinase) signalling pathways. Experimental data and computer simulations demonstrate that cross-talk is context-dependent and that both pathways can activate or inhibit each other. Positive influence of the PI3K pathway on the MAPK pathway is most effective at sufficiently low doses of growth factors, whereas negative influence of the MAPK pathway on the PI3K pathway is mostly pronounced at high doses of growth factors. Pathway cross-talk endows a cell with emerging capabilities for processing and decoding signals from multiple receptors activated by different combinations of extracellular cues.

摘要

在本文中,我们描述了 PI3K(磷酸肌醇 3-激酶)/Akt 和 Ras/MAPK(丝裂原激活蛋白激酶)信号通路之间的多层次串扰。实验数据和计算机模拟表明,串扰是上下文相关的,并且两条通路可以相互激活或抑制。在生长因子的剂量足够低时,PI3K 通路对 MAPK 通路的正向影响最为有效,而在生长因子的剂量足够高时,MAPK 通路对 PI3K 通路的负向影响最为显著。通路串扰赋予细胞处理和解码来自不同细胞外信号组合激活的多个受体的信号的新兴能力。

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