<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(23)</volume><submitter>Bonechi M</submitter><pubmed_abstract>The aim of this study was to investigate if thymidine kinase-1 (TK1), a well-known proliferation marker, could represent a valid circulating biomarker to identify hormone receptor positive (HR+)/HER2 negative (HER2neg) metastatic breast cancer (MBC) patients most likely to benefit from endocrine therapy (ET). We used the DiviTum™ assay to analyze TK1 activity in cell lysates of three HR+/HER2neg BC cell lines and in plasma of 31 HR+/HER2neg MBC patients receiving ET. Blood samples were collected at treatment initiation, after one month and at disease progression. CTCs count and &lt;i>ESR1&lt;/i>/&lt;i>PIK3CA&lt;/i> mutations in circulating tumor DNA were performed and correlated with TK1 activity. TK1 activity was reduced in the two endocrine-sensitive cell lines after 2 days of treatment. In patients</pubmed_abstract><journal>Oncotarget</journal><pagination>16389-16399</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5893248</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Plasma thymidine kinase-1 activity predicts outcome in patients with hormone receptor positive and HER2 negative metastatic breast cancer treated with endocrine therapy.</pubmed_title><pmcid>PMC5893248</pmcid><pubmed_authors>Biagioni C</pubmed_authors><pubmed_authors>Bergqvist M</pubmed_authors><pubmed_authors>Pestrin M</pubmed_authors><pubmed_authors>Galardi F</pubmed_authors><pubmed_authors>Gabellini S</pubmed_authors><pubmed_authors>Di Leo A</pubmed_authors><pubmed_authors>Malorni L</pubmed_authors><pubmed_authors>Boccalini G</pubmed_authors><pubmed_authors>Neumuller M</pubmed_authors><pubmed_authors>Guarducci C</pubmed_authors><pubmed_authors>De Luca F</pubmed_authors><pubmed_authors>Migliaccio I</pubmed_authors><pubmed_authors>Bonechi M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Plasma thymidine kinase-1 activity predicts outcome in patients with hormone receptor positive and HER2 negative metastatic breast cancer treated with endocrine therapy.</name><description>The aim of this study was to investigate if thymidine kinase-1 (TK1), a well-known proliferation marker, could represent a valid circulating biomarker to identify hormone receptor positive (HR+)/HER2 negative (HER2neg) metastatic breast cancer (MBC) patients most likely to benefit from endocrine therapy (ET). We used the DiviTum™ assay to analyze TK1 activity in cell lysates of three HR+/HER2neg BC cell lines and in plasma of 31 HR+/HER2neg MBC patients receiving ET. Blood samples were collected at treatment initiation, after one month and at disease progression. CTCs count and &lt;i>ESR1&lt;/i>/&lt;i>PIK3CA&lt;/i> mutations in circulating tumor DNA were performed and correlated with TK1 activity. TK1 activity was reduced in the two endocrine-sensitive cell lines after 2 days of treatment. In patients</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-18T13:08:54.383Z</modification><creation>2019-03-26T23:29:27Z</creation></dates><accession>S-EPMC5893248</accession><cross_references><pubmed>29662653</pubmed><doi>10.18632/oncotarget.24700</doi></cross_references></HashMap>