<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>127(10)</volume><submitter>Ingebriktsen LM</submitter><pubmed_abstract>&lt;h4>Background and objective&lt;/h4>Breast cancer (BC) diagnosed at ages &lt;40 years presents with more aggressive tumour phenotypes and poorer clinical outcome compared to older BC patients. Here, we explored transcriptional BC alterations to gain a better understanding of age-related tumour biology, also subtype-stratified.&lt;h4>Methods&lt;/h4>We studied publicly available global BC mRNA expression (n = 3999) and proteomics data (n = 113), exploring differentially expressed genes, enriched gene sets, and gene networks in the young compared to older patients.&lt;h4>Results&lt;/h4>We identified transcriptional patterns reflecting increased proliferation and oncogenic signalling in BC of the young, also in subtype-stratified analyses. Six up-regulated hub genes built a novel age-related score, significantl</pubmed_abstract><journal>British journal of cancer</journal><pagination>1865-1875</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9643541</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A novel age-related gene expression signature associates with proliferation and disease progression in breast cancer.</pubmed_title><pmcid>PMC9643541</pmcid><pubmed_authors>Wik E</pubmed_authors><pubmed_authors>Ingebriktsen LM</pubmed_authors><pubmed_authors>Akslen LA</pubmed_authors><pubmed_authors>Finne K</pubmed_authors></additional><is_claimable>false</is_claimable><name>A novel age-related gene expression signature associates with proliferation and disease progression in breast cancer.</name><description>&lt;h4>Background and objective&lt;/h4>Breast cancer (BC) diagnosed at ages &lt;40 years presents with more aggressive tumour phenotypes and poorer clinical outcome compared to older BC patients. Here, we explored transcriptional BC alterations to gain a better understanding of age-related tumour biology, also subtype-stratified.&lt;h4>Methods&lt;/h4>We studied publicly available global BC mRNA expression (n = 3999) and proteomics data (n = 113), exploring differentially expressed genes, enriched gene sets, and gene networks in the young compared to older patients.&lt;h4>Results&lt;/h4>We identified transcriptional patterns reflecting increased proliferation and oncogenic signalling in BC of the young, also in subtype-stratified analyses. Six up-regulated hub genes built a novel age-related score, significantl</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-18T19:06:37.198Z</modification><creation>2025-04-07T06:45:17.075Z</creation></dates><accession>S-EPMC9643541</accession><cross_references><pubmed>35995935</pubmed><doi>10.1038/s41416-022-01953-w</doi></cross_references></HashMap>