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PKCθ 介导的 FAK 丝氨酸/苏氨酸磷酸化调控乳腺癌细胞迁移过程中片状伪足内的黏附与延伸动力学。

PKCθ-mediated serine/threonine phosphorylations of FAK govern adhesion and protrusion dynamics within the lamellipodia of migrating breast cancer cells.

机构信息

MCD, Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, UPS, 31062, Toulouse, France.

Department of Pharmacology and Lineberger Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Cancer Lett. 2022 Feb 1;526:112-130. doi: 10.1016/j.canlet.2021.11.026. Epub 2021 Nov 23.

Abstract

The cytoskeleton and cell-matrix adhesions constitute a dynamic network that controls cellular behavior during development and cancer. The Focal Adhesion Kinase (FAK) is a central actor of these cell dynamics, promoting cell-matrix adhesion turnover and active membrane fluctuations. However, the initial steps leading to FAK activation and subsequent promotion of cell dynamics remain elusive. Here, we report that the serine/threonine kinase PKCθ participates in the initial steps of FAK activation. PKCθ, which is strongly expressed in aggressive human breast cancers, controls the dynamics of cell-matrix adhesions and active protrusions through direct FAK activation, thereby promoting cell invasion and lung metastases. Using various tools for in vitro and live cell studies, we precisely decipher the molecular mechanisms of FAK activation. PKCθ directly interacts with the FAK FERM domain to open FAK conformation through PKCθ's specific V3 domain, while phosphorylating FAK at newly identified serine/threonine residues within nascent adhesions, inducing cell dynamics and aggressive behavior. This study thus places PKCθ-directed FAK opening and phosphorylations as an original mechanism controlling dynamic, migratory, and invasive abilities of aggressive breast cancer cells, further strengthening the emerging oncogenic function of PKCθ.

摘要

细胞骨架和细胞基质黏附构成了一个动态网络,控制着发育和癌症过程中的细胞行为。粘着斑激酶(FAK)是这些细胞动力学的核心因子,促进细胞基质黏附的周转和活跃的膜波动。然而,导致 FAK 激活以及随后促进细胞动力学的初始步骤仍然难以捉摸。在这里,我们报告丝氨酸/苏氨酸激酶 PKCθ 参与 FAK 激活的初始步骤。在侵袭性强的人类乳腺癌中强烈表达的 PKCθ,通过直接 FAK 激活控制细胞基质黏附和活跃突起的动力学,从而促进细胞侵袭和肺转移。通过使用各种体外和活细胞研究工具,我们精确地破译了 FAK 激活的分子机制。PKCθ 通过其特有的 V3 结构域与 FAK 的 FERM 结构域直接相互作用,打开 FAK 的构象,同时在新形成的黏附处的丝氨酸/苏氨酸残基上磷酸化 FAK,诱导细胞动力学和侵袭行为。因此,这项研究将 PKCθ 定向的 FAK 开放和磷酸化作为一种原始机制,控制侵袭性乳腺癌细胞的动态、迁移和侵袭能力,进一步加强了 PKCθ 作为新兴致癌因子的功能。

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