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Signal integration in TGF-β, WNT, and Hippo pathways
Complete sequences of animal genomes have revealed a remarkably small and conserved toolbox of signalling pathways, such as TGF-β and WNT that account for all biological diversity. This raises the question as to how such a limited set of cues elaborates so many diverse cell fates and behaviours. It...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculty of 1000 Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672943/ https://www.ncbi.nlm.nih.gov/pubmed/23755364 http://dx.doi.org/10.12703/P5-17 |
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author | Attisano, Liliana Wrana, Jeffrey L. |
author_facet | Attisano, Liliana Wrana, Jeffrey L. |
author_sort | Attisano, Liliana |
collection | PubMed |
description | Complete sequences of animal genomes have revealed a remarkably small and conserved toolbox of signalling pathways, such as TGF-β and WNT that account for all biological diversity. This raises the question as to how such a limited set of cues elaborates so many diverse cell fates and behaviours. It is now clear that components of signalling pathways are physically assembled into higher order networks that ultimately dictate the biological output of pathway activity. Intertwining of pathways is thus emerging as a key feature of a large, integrated and coordinated signalling network that allows cells to read a limited set of extrinsic cues, but mount the diverse responses that underpin successful development and homeostasis. Moreover, this design principle confounds the development of effective therapeutic interventions in complex diseases, such as cancer. |
format | Online Article Text |
id | pubmed-3672943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Faculty of 1000 Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36729432013-06-10 Signal integration in TGF-β, WNT, and Hippo pathways Attisano, Liliana Wrana, Jeffrey L. F1000Prime Rep Review Article Complete sequences of animal genomes have revealed a remarkably small and conserved toolbox of signalling pathways, such as TGF-β and WNT that account for all biological diversity. This raises the question as to how such a limited set of cues elaborates so many diverse cell fates and behaviours. It is now clear that components of signalling pathways are physically assembled into higher order networks that ultimately dictate the biological output of pathway activity. Intertwining of pathways is thus emerging as a key feature of a large, integrated and coordinated signalling network that allows cells to read a limited set of extrinsic cues, but mount the diverse responses that underpin successful development and homeostasis. Moreover, this design principle confounds the development of effective therapeutic interventions in complex diseases, such as cancer. Faculty of 1000 Ltd 2013-06-03 /pmc/articles/PMC3672943/ /pubmed/23755364 http://dx.doi.org/10.12703/P5-17 Text en © 2013 Faculty of 1000 Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use this work for commercial purposes |
spellingShingle | Review Article Attisano, Liliana Wrana, Jeffrey L. Signal integration in TGF-β, WNT, and Hippo pathways |
title | Signal integration in TGF-β, WNT, and Hippo pathways |
title_full | Signal integration in TGF-β, WNT, and Hippo pathways |
title_fullStr | Signal integration in TGF-β, WNT, and Hippo pathways |
title_full_unstemmed | Signal integration in TGF-β, WNT, and Hippo pathways |
title_short | Signal integration in TGF-β, WNT, and Hippo pathways |
title_sort | signal integration in tgf-β, wnt, and hippo pathways |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672943/ https://www.ncbi.nlm.nih.gov/pubmed/23755364 http://dx.doi.org/10.12703/P5-17 |
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