Pan-Cancer Analysis of the Genomic Alterations and Mutations of the Matrisome

The extracellular matrix (ECM) is a master regulator of all cellular functions and a major component of the tumor microenvironment. We previously defined the "matrisome" as the ensemble of genes encoding ECM proteins and proteins modulating ECM structure or function. While compositional an...

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Main Authors: Valerio Izzi, Martin N. Davis, Alexandra Naba
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/12/8/2046
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spelling doaj-3bc9281c175a40fcbc54907d116d67ea2020-11-25T03:45:02ZengMDPI AGCancers2072-66942020-07-01122046204610.3390/cancers12082046Pan-Cancer Analysis of the Genomic Alterations and Mutations of the MatrisomeValerio Izzi0Martin N. Davis1Alexandra Naba2Faculty of Biochemistry and Molecular Medicine, University of Oulu, FI-90014 Oulu, FinlandDepartment of Physiology and Biophysics, University of Illinois at Chicago, Chicago, IL 60612, USADepartment of Physiology and Biophysics, University of Illinois at Chicago, Chicago, IL 60612, USAThe extracellular matrix (ECM) is a master regulator of all cellular functions and a major component of the tumor microenvironment. We previously defined the "matrisome" as the ensemble of genes encoding ECM proteins and proteins modulating ECM structure or function. While compositional and biomechanical changes in the ECM regulate cancer progression, no study has investigated the genomic alterations of matrisome genes in cancers and their consequences. Here, mining The Cancer Genome Atlas (TCGA) data, we found that copy number alterations and mutations are frequent in matrisome genes, even more so than in the rest of the genome. We also found that these alterations are predicted to significantly impact gene expression and protein function. Moreover, we identified matrisome genes whose mutational burden is an independent predictor of survival. We propose that studying genomic alterations of matrisome genes will further our understanding of the roles of this compartment in cancer progression and will lead to the development of innovative therapeutic strategies targeting the ECM.https://www.mdpi.com/2072-6694/12/8/2046extracellular matrixtumor microenvironmentcopy number alterationsmutationsprotein domainssurvival
collection DOAJ
language English
format Article
sources DOAJ
author Valerio Izzi
Martin N. Davis
Alexandra Naba
spellingShingle Valerio Izzi
Martin N. Davis
Alexandra Naba
Pan-Cancer Analysis of the Genomic Alterations and Mutations of the Matrisome
Cancers
extracellular matrix
tumor microenvironment
copy number alterations
mutations
protein domains
survival
author_facet Valerio Izzi
Martin N. Davis
Alexandra Naba
author_sort Valerio Izzi
title Pan-Cancer Analysis of the Genomic Alterations and Mutations of the Matrisome
title_short Pan-Cancer Analysis of the Genomic Alterations and Mutations of the Matrisome
title_full Pan-Cancer Analysis of the Genomic Alterations and Mutations of the Matrisome
title_fullStr Pan-Cancer Analysis of the Genomic Alterations and Mutations of the Matrisome
title_full_unstemmed Pan-Cancer Analysis of the Genomic Alterations and Mutations of the Matrisome
title_sort pan-cancer analysis of the genomic alterations and mutations of the matrisome
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2020-07-01
description The extracellular matrix (ECM) is a master regulator of all cellular functions and a major component of the tumor microenvironment. We previously defined the "matrisome" as the ensemble of genes encoding ECM proteins and proteins modulating ECM structure or function. While compositional and biomechanical changes in the ECM regulate cancer progression, no study has investigated the genomic alterations of matrisome genes in cancers and their consequences. Here, mining The Cancer Genome Atlas (TCGA) data, we found that copy number alterations and mutations are frequent in matrisome genes, even more so than in the rest of the genome. We also found that these alterations are predicted to significantly impact gene expression and protein function. Moreover, we identified matrisome genes whose mutational burden is an independent predictor of survival. We propose that studying genomic alterations of matrisome genes will further our understanding of the roles of this compartment in cancer progression and will lead to the development of innovative therapeutic strategies targeting the ECM.
topic extracellular matrix
tumor microenvironment
copy number alterations
mutations
protein domains
survival
url https://www.mdpi.com/2072-6694/12/8/2046
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AT martinndavis pancanceranalysisofthegenomicalterationsandmutationsofthematrisome
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