Transforming growth factor-β, MAPK and Wnt signaling interactions in colorectal cancer

Q4 Biochemistry, Genetics and Molecular Biology EuPA Open Proteomics Pub Date : 2015-09-01 DOI:10.1016/j.euprot.2015.06.004
Harish R. Cheruku , Abidali Mohamedali , David I. Cantor , Sock Hwee Tan , Edouard C. Nice , Mark S. Baker
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引用次数: 32

Abstract

In non-cancerous cells, transforming growth factor-β (TGFβ) regulates cellular responses primarily through Smad signaling. However, during cancer progression (including colorectal) TGFβ promotes tumoral growth via Smad-independent mechanisms and is involved in crosstalk with various pathways like the mitogen-activated protein kinases (MAPK) and Wnt. Crosstalk between these pathways following activation by TGFβ and subsequent downstream signaling activity can be referred to as a crosstalk signaling signature. This review highlights the progress in understanding TGFβ signaling crosstalk involving various MAPK pathway members (e.g., extracellular signal-regulated kinase (Erk) 1/2, Ras, c-Jun N-terminal kinases (JNK) and p38) and the Wnt signaling pathway.

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转化生长因子-β、MAPK和Wnt信号在结直肠癌中的相互作用
在非癌细胞中,转化生长因子-β (tgf -β)主要通过Smad信号调节细胞反应。然而,在癌症进展过程中(包括结直肠癌),TGFβ通过smad不依赖的机制促进肿瘤生长,并参与各种途径的串扰,如丝裂原活化蛋白激酶(MAPK)和Wnt。tgf - β激活后这些通路之间的串扰和随后的下游信号活动可被称为串扰信号特征。这篇综述强调了了解涉及各种MAPK通路成员(如细胞外信号调节激酶(Erk) 1/2、Ras、c-Jun n末端激酶(JNK)和p38)和Wnt信号通路的tgf - β信号串扰的进展。
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来源期刊
EuPA Open Proteomics
EuPA Open Proteomics Biochemistry, Genetics and Molecular Biology-Biochemistry
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Proceedings of the EuBIC-MS 2020 Developers’ Meeting Editorial: The next generation in (EuPA Open) Proteomics Aims & scope Proceedings of the EuBIC Winter School 2019 Introducing the YPIC challenge
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