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The p140Cap adaptor protein as a molecular hub to block cancer aggressiveness
The p140Cap adaptor protein is a scaffold molecule encoded by the SRCIN1 gene, which is physiologically expressed in several epithelial tissues and in the neurons. However, p140Cap is also strongly expressed in a significant subset of cancers including breast cancer and neuroblastoma. Notably, cance...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904710/ https://www.ncbi.nlm.nih.gov/pubmed/33079227 http://dx.doi.org/10.1007/s00018-020-03666-w |
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author | Salemme, Vincenzo Angelini, Costanza Chapelle, Jennifer Centonze, Giorgia Natalini, Dora Morellato, Alessandro Taverna, Daniela Turco, Emilia Ala, Ugo Defilippi, Paola |
author_facet | Salemme, Vincenzo Angelini, Costanza Chapelle, Jennifer Centonze, Giorgia Natalini, Dora Morellato, Alessandro Taverna, Daniela Turco, Emilia Ala, Ugo Defilippi, Paola |
author_sort | Salemme, Vincenzo |
collection | PubMed |
description | The p140Cap adaptor protein is a scaffold molecule encoded by the SRCIN1 gene, which is physiologically expressed in several epithelial tissues and in the neurons. However, p140Cap is also strongly expressed in a significant subset of cancers including breast cancer and neuroblastoma. Notably, cancer patients with high p140Cap expression in their primary tumors have a lower probability of developing a distant event and ERBB2-positive breast cancer sufferers show better survival. In neuroblastoma patients, SRCIN1 mRNA levels represent an independent risk factor, which is inversely correlated to disease aggressiveness. Consistent with clinical data, SRCIN1 gain or loss of function mouse models demonstrated that p140Cap may affect tumor growth and metastasis formation by controlling the signaling pathways involved in tumorigenesis and metastatic features. This study reviews data showing the relevance of SRCIN1/p140Cap in cancer patients, the impact of SRCIN1 status on p140Cap expression, the specific mechanisms through which p140Cap can limit cancer progression, the molecular functions regulated by p140Cap, along with the p140Cap interactome, to unveil its key role for patient stratification in clinics. |
format | Online Article Text |
id | pubmed-7904710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-79047102021-03-09 The p140Cap adaptor protein as a molecular hub to block cancer aggressiveness Salemme, Vincenzo Angelini, Costanza Chapelle, Jennifer Centonze, Giorgia Natalini, Dora Morellato, Alessandro Taverna, Daniela Turco, Emilia Ala, Ugo Defilippi, Paola Cell Mol Life Sci Review The p140Cap adaptor protein is a scaffold molecule encoded by the SRCIN1 gene, which is physiologically expressed in several epithelial tissues and in the neurons. However, p140Cap is also strongly expressed in a significant subset of cancers including breast cancer and neuroblastoma. Notably, cancer patients with high p140Cap expression in their primary tumors have a lower probability of developing a distant event and ERBB2-positive breast cancer sufferers show better survival. In neuroblastoma patients, SRCIN1 mRNA levels represent an independent risk factor, which is inversely correlated to disease aggressiveness. Consistent with clinical data, SRCIN1 gain or loss of function mouse models demonstrated that p140Cap may affect tumor growth and metastasis formation by controlling the signaling pathways involved in tumorigenesis and metastatic features. This study reviews data showing the relevance of SRCIN1/p140Cap in cancer patients, the impact of SRCIN1 status on p140Cap expression, the specific mechanisms through which p140Cap can limit cancer progression, the molecular functions regulated by p140Cap, along with the p140Cap interactome, to unveil its key role for patient stratification in clinics. Springer International Publishing 2020-10-20 2021 /pmc/articles/PMC7904710/ /pubmed/33079227 http://dx.doi.org/10.1007/s00018-020-03666-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Salemme, Vincenzo Angelini, Costanza Chapelle, Jennifer Centonze, Giorgia Natalini, Dora Morellato, Alessandro Taverna, Daniela Turco, Emilia Ala, Ugo Defilippi, Paola The p140Cap adaptor protein as a molecular hub to block cancer aggressiveness |
title | The p140Cap adaptor protein as a molecular hub to block cancer aggressiveness |
title_full | The p140Cap adaptor protein as a molecular hub to block cancer aggressiveness |
title_fullStr | The p140Cap adaptor protein as a molecular hub to block cancer aggressiveness |
title_full_unstemmed | The p140Cap adaptor protein as a molecular hub to block cancer aggressiveness |
title_short | The p140Cap adaptor protein as a molecular hub to block cancer aggressiveness |
title_sort | p140cap adaptor protein as a molecular hub to block cancer aggressiveness |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904710/ https://www.ncbi.nlm.nih.gov/pubmed/33079227 http://dx.doi.org/10.1007/s00018-020-03666-w |
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