<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pedersen CA</submitter><funding>Liaison committee between the Central Norway Health Authority and NTNU</funding><funding>Stiftelsen Kristian Gerhard Jebsen</funding><funding>Kreftforeningen, Norway</funding><funding>NTNU Norwegian University of Science and Technology</funding><funding>Kreftforeningen</funding><funding>The joint research committee between St. Olavs Hospital and the Faculty of Medicine and Health Sciences, NTNU</funding><funding>Horizon 2020</funding><pagination>43</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9233373</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Locally advanced breast cancer is a heterogeneous disease with respect to response to neoadjuvant chemotherapy (NACT) and survival. It is currently not possible to accurately predict who will benefit from the specific types of NACT. DNA methylation is an epigenetic mechanism known to play an important role in regulating gene expression and may serve as a biomarker for treatment response and survival. We investigated the potential role of DNA methylation as a prognostic marker for long-term survival (> 5 years) after NACT in breast cancer.&lt;h4>Methods&lt;/h4>DNA methylation profiles of pre-treatment (n = 55) and post-treatment (n = 75) biopsies from 83 women with locally advanced breast cancer were investigated using the Illumina HumanMethylation450 BeadChip. The patients rec</pubmed_abstract><journal>Breast cancer research : BCR</journal><pubmed_title>DNA methylation changes in response to neoadjuvant chemotherapy are associated with breast cancer survival.</pubmed_title><pmcid>PMC9233373</pmcid><funding_grant_id>758306</funding_grant_id><funding_grant_id>202021</funding_grant_id><funding_grant_id>28328</funding_grant_id><funding_grant_id>6834362</funding_grant_id><pubmed_authors>Eikesdal HP</pubmed_authors><pubmed_authors>Giskeodegard GF</pubmed_authors><pubmed_authors>Rye MB</pubmed_authors><pubmed_authors>Lonning PE</pubmed_authors><pubmed_authors>Bathen TF</pubmed_authors><pubmed_authors>Pedersen CA</pubmed_authors><pubmed_authors>Kristensen VN</pubmed_authors><pubmed_authors>Cao MD</pubmed_authors><pubmed_authors>Fleischer T</pubmed_authors><pubmed_authors>Tessem MB</pubmed_authors><pubmed_authors>Knappskog S</pubmed_authors><pubmed_authors>Tost J</pubmed_authors></additional><is_claimable>false</is_claimable><name>DNA methylation changes in response to neoadjuvant chemotherapy are associated with breast cancer survival.</name><description>&lt;h4>Background&lt;/h4>Locally advanced breast cancer is a heterogeneous disease with respect to response to neoadjuvant chemotherapy (NACT) and survival. It is currently not possible to accurately predict who will benefit from the specific types of NACT. DNA methylation is an epigenetic mechanism known to play an important role in regulating gene expression and may serve as a biomarker for treatment response and survival. We investigated the potential role of DNA methylation as a prognostic marker for long-term survival (> 5 years) after NACT in breast cancer.&lt;h4>Methods&lt;/h4>DNA methylation profiles of pre-treatment (n = 55) and post-treatment (n = 75) biopsies from 83 women with locally advanced breast cancer were investigated using the Illumina HumanMethylation450 BeadChip. The patients rec</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-04-04T19:13:20.221Z</modification><creation>2025-04-04T19:13:20.221Z</creation></dates><accession>S-EPMC9233373</accession><cross_references><pubmed>35751095</pubmed><doi>10.1186/s13058-022-01537-9</doi></cross_references></HashMap>