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Src/FAK-mediated regulation of E-cadherin as a mechanism for controlling collective cell movement: Insights from in vivo imaging

机译:Src / FAK介导的E-钙粘蛋白调节作为控制集体细胞运动的机制:体内成像的见解

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摘要

Recent advances in confocal and multi-photon microscopy, together with fluorescent probe development, have enabled cancer biology studies to go beyond the culture dish and interrogate cancer-associated processes in the complex in vivo environment. Regulation of the tumor suppressor protein E-cadherin plays an important role in cancer development and progression, and may contribute to the decision between 'single cell' and 'collective invasion' in vivo. Mounting evidence from in vitro and in vivo experiments places the two nonreceptor protein tyrosine kinases Src and Focal Adhesion Kinase at the heart of E-cadherin regulation and the crosstalk between integrins and cadherins. Here we discuss recent insights, attained using high-resolution fluorescent in vivo imaging, into the regulation of E-cadherin and collective invasion. We focus on the regulatory crosstalk between the Src/FAK signaling axis and E-cadherin in vivo.
机译:共聚焦和多光子显微镜的最新进展,以及荧光探针的发展,已经使癌症生物学研究超越了培养皿,并且可以在复杂的体内环境中研究与癌症相关的过程。肿瘤抑制蛋白E-cadherin的调节在癌症的发展和进程中起着重要作用,并且可能有助于体内“单细胞”和“集体侵袭”之间的决定。来自体外和体内实验的越来越多的证据将两种非受体蛋白酪氨酸激酶Src和Focal Adhesion Kinase置于E-cadherin调控的核心,以及整联蛋白与钙粘着蛋白之间的串扰。在这里,我们讨论使用高分辨率的荧光体内成像获得的有关E-钙粘蛋白和集体侵袭调节的最新见解。我们专注于体内Src / FAK信号轴和E-钙粘蛋白之间的调控串扰。

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