<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(44)</volume><submitter>Gay-Bellile M</submitter><pubmed_abstract>Upregulation of the telomerase reverse transcriptase (&lt;i>TERT&lt;/i>) gene in human cancers leads to telomerase activation, which contributes to the growth advantage and survival of tumor cells. Molecular mechanisms of &lt;i>TERT&lt;/i> upregulation are complex, tumor-specific and can be clinically relevant. To investigate these mechanisms in breast cancer, we sequenced the &lt;i>TERT&lt;/i> promoter, evaluated &lt;i>TERT&lt;/i> copy number changes and assessed the expression of the &lt;i>MYC&lt;/i> oncogene, a known transcriptional &lt;i>TERT&lt;/i> regulator, in two breast cancer cohorts comprising a total of 122 patients. No activating &lt;i>TERT&lt;/i> promoter mutations were found, suggesting that this mutational mechanism is not likely to be involved in &lt;i>TERT&lt;/i> upregulation in breast cancer. The T349C promoter polymor</pubmed_abstract><journal>Oncotarget</journal><pagination>77540-77551</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5652798</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;i>TERT&lt;/i> promoter status and gene copy number gains: effect on &lt;i>TERT&lt;/i> expression and association with prognosis in breast cancer.</pubmed_title><pmcid>PMC5652798</pmcid><pubmed_authors>Bignon YJ</pubmed_authors><pubmed_authors>Combes P</pubmed_authors><pubmed_authors>Tchirkov A</pubmed_authors><pubmed_authors>Cayre A</pubmed_authors><pubmed_authors>Abrial C</pubmed_authors><pubmed_authors>Vago P</pubmed_authors><pubmed_authors>Dauplat MM</pubmed_authors><pubmed_authors>Privat M</pubmed_authors><pubmed_authors>Eymard-Pierre E</pubmed_authors><pubmed_authors>Penault-Llorca F</pubmed_authors><pubmed_authors>Gay-Bellile M</pubmed_authors><pubmed_authors>Kwiatkowski F</pubmed_authors><pubmed_authors>Mouret-Reynier MA</pubmed_authors><pubmed_authors>Veronese L</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>TERT&lt;/i> promoter status and gene copy number gains: effect on &lt;i>TERT&lt;/i> expression and association with prognosis in breast cancer.</name><description>Upregulation of the telomerase reverse transcriptase (&lt;i>TERT&lt;/i>) gene in human cancers leads to telomerase activation, which contributes to the growth advantage and survival of tumor cells. Molecular mechanisms of &lt;i>TERT&lt;/i> upregulation are complex, tumor-specific and can be clinically relevant. To investigate these mechanisms in breast cancer, we sequenced the &lt;i>TERT&lt;/i> promoter, evaluated &lt;i>TERT&lt;/i> copy number changes and assessed the expression of the &lt;i>MYC&lt;/i> oncogene, a known transcriptional &lt;i>TERT&lt;/i> regulator, in two breast cancer cohorts comprising a total of 122 patients. No activating &lt;i>TERT&lt;/i> promoter mutations were found, suggesting that this mutational mechanism is not likely to be involved in &lt;i>TERT&lt;/i> upregulation in breast cancer. The T349C promoter polymor</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Sep</publication><modification>2026-04-29T09:53:45.003Z</modification><creation>2019-03-27T02:59:41Z</creation></dates><accession>S-EPMC5652798</accession><cross_references><pubmed>29100407</pubmed><doi>10.18632/oncotarget.20560</doi></cross_references></HashMap>