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整合素作为病理性血管生成调控中的“功能枢纽”。

Integrins as "functional hubs" in the regulation of pathological angiogenesis.

机构信息

Maine Medical Center Research Institute, Center for Molecular Medicine, 81 Research Drive, Scarborough, ME 04074, United States.

出版信息

Semin Cancer Biol. 2009 Oct;19(5):318-28. doi: 10.1016/j.semcancer.2009.05.002. Epub 2009 May 29.

Abstract

It is well accepted that complex biological processes such as angiogenesis are not controlled by a single family of molecules or individually isolated signaling pathways. In this regard, new insight into the interconnected mechanisms that regulate angiogenesis might be gained by examining this process from a more global network perspective. The coordination of signaling cues from both outside and inside many different cell types is required for the successful completion of angiogenesis. Evidence is accumulating that the multifunctional integrin family of cell adhesion receptors represent an important group of molecules that play active roles in sensing, integrating, and distributing a diverse set of signals that regulate many cellular events required for angiogenesis. Given the ability of integrins to bind numerous extracellular ligands and transmit signals in a bi-directional fashion, we will discuss the multiple ways by which integrins may serve as a functional hub during pathological angiogenesis. In addition, we will highlight potential imaging and therapeutic strategies based on the expanding new insight into integrin function.

摘要

人们普遍认为,血管生成等复杂的生物过程不是由单一的分子家族或单独分离的信号通路控制的。在这方面,通过从更全局的网络角度来研究这个过程,可能会对调节血管生成的相互关联的机制有新的认识。来自许多不同细胞类型内外的信号的协调是血管生成成功完成所必需的。有证据表明,多功能整合素细胞粘附受体家族代表了一组重要的分子,它们在感知、整合和分配调节血管生成所需的许多细胞事件的多样化信号方面发挥着积极作用。鉴于整合素能够结合许多细胞外配体并以双向方式传递信号,我们将讨论整合素在病理性血管生成过程中作为功能枢纽的多种方式。此外,我们将根据对整合素功能的不断扩大的新认识,强调潜在的成像和治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed0c/2806796/b2e3f418989d/nihms165824f1.jpg

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