Cargando…
Cancer associated talin point mutations disorganise cell adhesion and migration
Talin-1 is a key component of the multiprotein adhesion complexes which mediate cell migration, adhesion and integrin signalling and has been linked to cancer in several studies. We analysed talin-1 mutations reported in the Catalogue of Somatic Mutations in Cancer database and developed a bioinform...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801617/ https://www.ncbi.nlm.nih.gov/pubmed/33431906 http://dx.doi.org/10.1038/s41598-020-77911-4 |
_version_ | 1783635612398518272 |
---|---|
author | Azizi, Latifeh Cowell, Alana R. Mykuliak, Vasyl V. Goult, Benjamin T. Turkki, Paula Hytönen, Vesa P. |
author_facet | Azizi, Latifeh Cowell, Alana R. Mykuliak, Vasyl V. Goult, Benjamin T. Turkki, Paula Hytönen, Vesa P. |
author_sort | Azizi, Latifeh |
collection | PubMed |
description | Talin-1 is a key component of the multiprotein adhesion complexes which mediate cell migration, adhesion and integrin signalling and has been linked to cancer in several studies. We analysed talin-1 mutations reported in the Catalogue of Somatic Mutations in Cancer database and developed a bioinformatics pipeline to predict the severity of each mutation. These predictions were then assessed using biochemistry and cell biology experiments. With this approach we were able to identify several talin-1 mutations affecting integrin activity, actin recruitment and Deleted in Liver Cancer 1 localization. We explored potential changes in talin-1 signalling responses by assessing impact on migration, invasion and proliferation. Altogether, this study describes a pipeline approach of experiments for crude characterization of talin-1 mutants in order to evaluate their functional effects and potential pathogenicity. Our findings suggest that cancer related point mutations in talin-1 can affect cell behaviour and so may contribute to cancer progression. |
format | Online Article Text |
id | pubmed-7801617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78016172021-01-12 Cancer associated talin point mutations disorganise cell adhesion and migration Azizi, Latifeh Cowell, Alana R. Mykuliak, Vasyl V. Goult, Benjamin T. Turkki, Paula Hytönen, Vesa P. Sci Rep Article Talin-1 is a key component of the multiprotein adhesion complexes which mediate cell migration, adhesion and integrin signalling and has been linked to cancer in several studies. We analysed talin-1 mutations reported in the Catalogue of Somatic Mutations in Cancer database and developed a bioinformatics pipeline to predict the severity of each mutation. These predictions were then assessed using biochemistry and cell biology experiments. With this approach we were able to identify several talin-1 mutations affecting integrin activity, actin recruitment and Deleted in Liver Cancer 1 localization. We explored potential changes in talin-1 signalling responses by assessing impact on migration, invasion and proliferation. Altogether, this study describes a pipeline approach of experiments for crude characterization of talin-1 mutants in order to evaluate their functional effects and potential pathogenicity. Our findings suggest that cancer related point mutations in talin-1 can affect cell behaviour and so may contribute to cancer progression. Nature Publishing Group UK 2021-01-11 /pmc/articles/PMC7801617/ /pubmed/33431906 http://dx.doi.org/10.1038/s41598-020-77911-4 Text en © The Author(s) 2021 Open Access This 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 | Article Azizi, Latifeh Cowell, Alana R. Mykuliak, Vasyl V. Goult, Benjamin T. Turkki, Paula Hytönen, Vesa P. Cancer associated talin point mutations disorganise cell adhesion and migration |
title | Cancer associated talin point mutations disorganise cell adhesion and migration |
title_full | Cancer associated talin point mutations disorganise cell adhesion and migration |
title_fullStr | Cancer associated talin point mutations disorganise cell adhesion and migration |
title_full_unstemmed | Cancer associated talin point mutations disorganise cell adhesion and migration |
title_short | Cancer associated talin point mutations disorganise cell adhesion and migration |
title_sort | cancer associated talin point mutations disorganise cell adhesion and migration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801617/ https://www.ncbi.nlm.nih.gov/pubmed/33431906 http://dx.doi.org/10.1038/s41598-020-77911-4 |
work_keys_str_mv | AT azizilatifeh cancerassociatedtalinpointmutationsdisorganisecelladhesionandmigration AT cowellalanar cancerassociatedtalinpointmutationsdisorganisecelladhesionandmigration AT mykuliakvasylv cancerassociatedtalinpointmutationsdisorganisecelladhesionandmigration AT goultbenjamint cancerassociatedtalinpointmutationsdisorganisecelladhesionandmigration AT turkkipaula cancerassociatedtalinpointmutationsdisorganisecelladhesionandmigration AT hytonenvesap cancerassociatedtalinpointmutationsdisorganisecelladhesionandmigration |