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首页> 外文期刊>Journal of molecular cell biology >Network-based identification of feedback modules that control RhoA activity and cell migration
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Network-based identification of feedback modules that control RhoA activity and cell migration

机译:基于网络的反馈模块的识别,控制ROOA活动和细胞迁移

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摘要

Cancer cell migration enables metastatic spread causing most cancer deaths. Rho-family GTPases control cell migration, but being embedded in a highly interconnected feedback network, the control of their dynamical behavior during cell migration remains elusive. To address this question, we reconstructed the Rho-family GTPases signaling network involved in cell migration, and developed a Boolean network model to analyze the different states and emergent rewiring of the Rho-family GTPases signaling network at protrusions and during extracellular matrix-dependent cell migration. Extensive simulations and experimental validations revealed that the bursts of RhoA activity induced at protrusions by EGF are regulated by a negative-feedback module composed of Src, FAK, and CSK. Interestingly, perturbing this module interfered with cyclic Rho activation and extracellular matrix-dependent migration, suggesting that CSK inhibition can be a novel and effective intervention strategy for blocking extracellular matrix-dependent cancer cell migration, while Src inhibition might fail, depending on the genetic background of cells. Thus, this study provides new insights into the mechanisms that regulate the intricate activation states of Rho-family GTPases during extracellular matrix-dependent migration, revealing potential new targets for interfering with extracellular matrix-dependent cancer cell migration.
机译:癌细胞迁移使转移传播能够导致大多数癌症死亡。 Rho-Family GTPAses控制单元迁移,但嵌入在高度互连的反馈网络中,控制细胞迁移期间的动态行为仍然难以捉摸。为了解决这个问题,我们重建了涉及细胞迁移的Rho-Family GTPAses信令网络,并开发了一个布尔网络模型,分析了突起和细胞外基质依赖性细胞中的rho-family gtpases信号通信网络的不同状态和紧急重新启动移民。广泛的模拟和实验验证揭示了通过EGF在突起中诱导的RHOA活性的突发由由SRC,FAK和CSK组成的负反馈模块来调节。有趣的是,该模块干扰了循环rhO活化和细胞外基质依赖的迁移,表明CSK抑制可以是阻断细胞外基质依赖性癌细胞迁移的新颖有效干预策略,而SRC抑制可能会失败,这取决于遗传背景细胞。因此,本研究为在细胞外基质依赖的迁移过程中调节Rho-Family GTP酶的复杂活化状态的机制提供了新的见解,揭示了干扰细胞外基质依赖性癌细胞迁移的潜在新靶标。

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