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TGIF1-Twist1 axis in pancreatic ductal adenocarcinoma

TG-interacting factor 1 (TGIF1) exerts inhibitory effects on transforming growth factor-beta (TGF-β) signaling by suppressing Smad signaling pathway at multiple levels. TGIF1 activity is important for normal embryogenesis and organogenesis, yet its dysregulation can culminate in tumorigenesis. For i...

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Detalles Bibliográficos
Autores principales: Razzaque, Mohammed S., Atfi, Azeddine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520386/
https://www.ncbi.nlm.nih.gov/pubmed/33005315
http://dx.doi.org/10.1016/j.csbj.2020.09.023
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author Razzaque, Mohammed S.
Atfi, Azeddine
author_facet Razzaque, Mohammed S.
Atfi, Azeddine
author_sort Razzaque, Mohammed S.
collection PubMed
description TG-interacting factor 1 (TGIF1) exerts inhibitory effects on transforming growth factor-beta (TGF-β) signaling by suppressing Smad signaling pathway at multiple levels. TGIF1 activity is important for normal embryogenesis and organogenesis, yet its dysregulation can culminate in tumorigenesis. For instance, increased expression of TGIF1 correlates with poor prognosis in triple-negative breast cancer patients, and enforced expression of TGIF1 facilitates Wnt-driven mammary tumorigenesis, suggesting that TGIF1 might function as an oncoprotein. Quite surprisingly, TGIF1 has recently been shown to function as a tumor suppressor in pancreatic ductal adenocarcinoma (PDAC), possibly owing to its ability to antagonize the pro-malignant transcription factor Twist1. In this article, we will briefly elaborate on the biological and clinical significance of the unique tumor-suppressive function of TGIF1 and its functional interaction with Twist1 in the context of PDAC pathogenesis and progression.
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spelling pubmed-75203862020-09-30 TGIF1-Twist1 axis in pancreatic ductal adenocarcinoma Razzaque, Mohammed S. Atfi, Azeddine Comput Struct Biotechnol J Review Article TG-interacting factor 1 (TGIF1) exerts inhibitory effects on transforming growth factor-beta (TGF-β) signaling by suppressing Smad signaling pathway at multiple levels. TGIF1 activity is important for normal embryogenesis and organogenesis, yet its dysregulation can culminate in tumorigenesis. For instance, increased expression of TGIF1 correlates with poor prognosis in triple-negative breast cancer patients, and enforced expression of TGIF1 facilitates Wnt-driven mammary tumorigenesis, suggesting that TGIF1 might function as an oncoprotein. Quite surprisingly, TGIF1 has recently been shown to function as a tumor suppressor in pancreatic ductal adenocarcinoma (PDAC), possibly owing to its ability to antagonize the pro-malignant transcription factor Twist1. In this article, we will briefly elaborate on the biological and clinical significance of the unique tumor-suppressive function of TGIF1 and its functional interaction with Twist1 in the context of PDAC pathogenesis and progression. Research Network of Computational and Structural Biotechnology 2020-09-17 /pmc/articles/PMC7520386/ /pubmed/33005315 http://dx.doi.org/10.1016/j.csbj.2020.09.023 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Razzaque, Mohammed S.
Atfi, Azeddine
TGIF1-Twist1 axis in pancreatic ductal adenocarcinoma
title TGIF1-Twist1 axis in pancreatic ductal adenocarcinoma
title_full TGIF1-Twist1 axis in pancreatic ductal adenocarcinoma
title_fullStr TGIF1-Twist1 axis in pancreatic ductal adenocarcinoma
title_full_unstemmed TGIF1-Twist1 axis in pancreatic ductal adenocarcinoma
title_short TGIF1-Twist1 axis in pancreatic ductal adenocarcinoma
title_sort tgif1-twist1 axis in pancreatic ductal adenocarcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520386/
https://www.ncbi.nlm.nih.gov/pubmed/33005315
http://dx.doi.org/10.1016/j.csbj.2020.09.023
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