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癌症中与YAP/TEAD信号传导之间功能相互作用的计算机模拟分析。

Analysis in silico of the functional interaction between and YAP/TEAD signaling in cancer.

作者信息

Astudillo Pablo

机构信息

Instituto de Ciencias Biomédicas, Facultad de Ciencias de la Salud, Universidad Autónoma de Chile, Santiago, Chile.

出版信息

PeerJ. 2021 Feb 17;9:e10869. doi: 10.7717/peerj.10869. eCollection 2021.

DOI:10.7717/peerj.10869
PMID:33643710
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7896511/
Abstract

To date, most data regarding the crosstalk between the Wnt signaling pathway and the YAP/TAZ transcriptional coactivators focuses on the Wnt/β-catenin branch of the pathway. In contrast, the relationship between the non-canonical Wnt pathway and YAP/TAZ remains significantly less explored. Wnt5a is usually regarded as a prototypical non-canonical Wnt ligand, and its expression has been related to cancer progression. On the other hand, YAP/TAZ transcriptional coactivators act in concert with TEAD transcription factors to control gene expression. Although one article has shown previously that is a YAP/TEAD target gene, there is a need for further evidence supporting this regulatory relationship, because a possible YAP/Wnt5a regulatory circuit might have profound implications for cancer biology. This article analyzes publicly available ChIP-Seq, gene expression, and protein expression data to explore this relationship, and shows that might be a YAP/TEAD target gene in several contexts. Moreover, Wnt5a and YAP expression are significantly correlated in specific cancer types, suggesting that the crosstalk between YAP/TAZ and the Wnt pathway is more intricate than previously thought.

摘要

迄今为止,大多数关于Wnt信号通路与YAP/TAZ转录共激活因子之间相互作用的数据都集中在该通路的Wnt/β-连环蛋白分支上。相比之下,非经典Wnt通路与YAP/TAZ之间的关系仍有待深入探索。Wnt5a通常被视为典型的非经典Wnt配体,其表达与癌症进展有关。另一方面,YAP/TAZ转录共激活因子与TEAD转录因子协同作用来控制基因表达。尽管之前有一篇文章表明 是一个YAP/TEAD靶基因,但仍需要进一步的证据来支持这种调控关系,因为可能存在的YAP/Wnt5a调控回路可能对癌症生物学具有深远影响。本文分析了公开可用的ChIP-Seq、基因表达和蛋白质表达数据以探索这种关系,并表明 在多种情况下可能是一个YAP/TEAD靶基因。此外,Wnt5a和YAP的表达在特定癌症类型中显著相关,这表明YAP/TAZ与Wnt通路之间的相互作用比之前认为的更为复杂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/5f5eefd5c393/peerj-09-10869-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/3c227082f656/peerj-09-10869-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/4f129ba4d06b/peerj-09-10869-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/31501dbed923/peerj-09-10869-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/2a45221735e9/peerj-09-10869-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/5f5eefd5c393/peerj-09-10869-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/3c227082f656/peerj-09-10869-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/4f129ba4d06b/peerj-09-10869-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/31501dbed923/peerj-09-10869-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/2a45221735e9/peerj-09-10869-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0e8/7896511/5f5eefd5c393/peerj-09-10869-g005.jpg

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