tgf β诱导的上皮向间质过渡和转移中的网络基序和高基序

Gottumukkala Sai Bhavani, A. Palanisamy
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摘要

上皮-间充质转化(EMT)是一个复杂、非线性、动态的多步骤过程,在转移性癌症的发展中起着不可或缺的作用。观察到多种信号分子及其相关途径参与促进EMT和癌症转移。转化生长因子-β(TGFβ)通过其SMAD依赖性和SMAD非依赖性信号传导,协调了许多聚集在关键EMT转录因子(TF)上的调节因子。这些TF进一步控制癌症细胞从上皮状态向间充质状态的表型转变。本研究探讨了TGFβ信号通路及其独特的网络结构,以了解其在EMT中的信息处理作用。观察到两个连贯的1型前馈网络基序调节SNAIL和N-钙粘蛋白的表达。SNAIL是EMT的关键调节因子之一,它将导致超基序样结构的相干1型前馈环(C1FFL)连接起来(Adler和Medzhitov,2022)。对这些基序和超基序的系统建模和分析说明了所涉及的调节因子的几个有趣的突发信息处理作用。正如文献中所描述的,这些调节因子的已知作用与观察到的涌现特性高度相关。这些基序说明了在调节SNAIL和N-钙粘蛋白表达中的持久性检测和噪声过滤。除了这些系统级特性外,超基序结构还表现出GLI、SNAIL、ZEB和N-钙粘蛋白的时间表达。此外,假设并分析了一个假设的三层C1FFL超基序。分析揭示了各种有趣的系统级特性。然而,这种真实的生物网络的可能存在需要进一步的理论和实验探索。解码这些网络基序和超基序提供了对复杂生物现象的额外理解,例如癌症转移中的EMT。
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Network motifs and hypermotifs in TGFβ-induced epithelial to mesenchymal transition and metastasis
Epithelial to mesenchymal transition (EMT) is a complex, non-linear, dynamic multistep process that plays an integral role in the development of metastatic cancers. A diverse range of signaling molecules, along with their associated pathways, were observed to be involved in promoting EMT and cancer metastasis. Transforming growth factor–β (TGFβ), through its SMAD-dependent and SMAD-independent signaling, orchestrates numerous regulators that converge on key EMT transcription factors (TFs). These TFs further govern the phenotypic transition of cancer cells from epithelial to mesenchymal states. This study explores the TGFβ signaling pathway and its unique network architecture to understand their information processing roles in EMT. Two coherent type 1 feed forward network motifs regulating the expression of SNAIL and N-cadherin were observed. SNAIL, which is one of the crucial regulators of EMT, links both the coherent type 1 feed forward loops (C1FFLs) leading to hypermotif-like structure (Adler and Medzhitov, 2022). Systems modeling and analysis of these motifs and hypermotifs illustrated several interesting emergent information processing roles of the regulators involved. The known roles of these regulators, as described in the literature, were highly correlated with the emergent properties observed. The motifs illustrated persistence detection and noise filtration in regulating the expression of SNAIL and N-cadherin. Along with these system-level properties, the hypermotif architecture also exhibited temporal expression of GLI, SNAIL, ZEB, and N-cadherin. Furthermore, a hypothetical three-layered C1FFL hypermotif was postulated and analyzed. The analysis revealed various interesting system-level properties. However, possible existence of such real biological networks needs further exploration both theoretically and experimentally. Deciphering these network motifs and hypermotifs has provided an additional understanding of the complex biological phenomenon, such as EMT in cancer metastasis.
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