<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Alexandrou S</submitter><funding>National Breast Cancer Foundation</funding><pagination>E667</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6387372</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(3)</volume><pubmed_abstract>Basal-like breast cancer (BLBC) is an aggressive molecular subtype that represents up to 15% of breast cancers. It occurs in younger patients, and typically shows rapid development of locoregional and distant metastasis, resulting in a relatively high mortality rate. Its defining features are that it is positive for basal cytokeratins and, epidermal growth factor receptor and/or c-Kit. Problematically, it is typically negative for the estrogen receptor and human epidermal growth factor receptor 2 (HER2), which means that it is unsuitable for either hormone therapy or targeted HER2 therapy. As a result, there are few therapeutic options for BLBC, and a major priority is to define molecular subgroups of BLBC that could be targeted therapeutically. In this review, we focus on the highly proliferative and anti-apoptotic phenotype of BLBC with the goal of defining potential therapeutic avenues, which could take advantage of these aspects of tumor development.</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>The Proliferative and Apoptotic Landscape of Basal-like Breast Cancer.</pubmed_title><pmcid>PMC6387372</pmcid><funding_grant_id>EC-17-002</funding_grant_id><funding_grant_id>ECF-17-002</funding_grant_id><pubmed_authors>Alexandrou S</pubmed_authors><pubmed_authors>Caldon CE</pubmed_authors><pubmed_authors>Lim E</pubmed_authors><pubmed_authors>Ormandy CJ</pubmed_authors><pubmed_authors>Oakes SR</pubmed_authors><pubmed_authors>George SM</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Proliferative and Apoptotic Landscape of Basal-like Breast Cancer.</name><description>Basal-like breast cancer (BLBC) is an aggressive molecular subtype that represents up to 15% of breast cancers. It occurs in younger patients, and typically shows rapid development of locoregional and distant metastasis, resulting in a relatively high mortality rate. Its defining features are that it is positive for basal cytokeratins and, epidermal growth factor receptor and/or c-Kit. Problematically, it is typically negative for the estrogen receptor and human epidermal growth factor receptor 2 (HER2), which means that it is unsuitable for either hormone therapy or targeted HER2 therapy. As a result, there are few therapeutic options for BLBC, and a major priority is to define molecular subgroups of BLBC that could be targeted therapeutically. In this review, we focus on the highly proliferative and anti-apoptotic phenotype of BLBC with the goal of defining potential therapeutic avenues, which could take advantage of these aspects of tumor development.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Feb</publication><modification>2024-11-08T09:35:59.556Z</modification><creation>2019-06-06T20:53:55Z</creation></dates><accession>S-EPMC6387372</accession><cross_references><pubmed>30720718</pubmed><doi>10.3390/ijms20030667</doi></cross_references></HashMap>