<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fina E</submitter><funding>Associazione Italiana per la Ricerca sul Cancro</funding><funding>Fondazione Umberto Veronesi</funding><funding>Fondazione Italiana per la Ricerca sul Cancro</funding><pagination>78</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8876758</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>41(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Progression to stage IV disease remains the main cause of breast cancer-related deaths. Increasing knowledge on the hematogenous phase of metastasis is key for exploiting the entire window of opportunity to interfere with early dissemination and to achieve a more effective disease control. Recent evidence suggests that circulating tumor cells (CTCs) possess diverse adaptive mechanisms to survive in blood and eventually metastasize, encouraging research into CTC-directed therapies.&lt;h4>Methods&lt;/h4>On the hypothesis that the distinguishing molecular features of CTCs reveal useful information on metastasis biology and disease outcome, we compared the transcriptome of CTCs, primary tumors, lymph-node and lung metastases of the MDA-MB-231 xenograft model, and assessed the biol</pubmed_abstract><journal>Journal of experimental &amp; clinical cancer research : CR</journal><pubmed_title>Gene signatures of circulating breast cancer cell models are a source of novel molecular determinants of metastasis and improve circulating tumor cell detection in patients.</pubmed_title><pmcid>PMC8876758</pmcid><funding_grant_id>IG 16900</funding_grant_id><funding_grant_id>Fellowship 16411</funding_grant_id><funding_grant_id>Postdoctoral fellowships</funding_grant_id><pubmed_authors>Ciniselli CM</pubmed_authors><pubmed_authors>Fina E</pubmed_authors><pubmed_authors>Lecchi M</pubmed_authors><pubmed_authors>Bianchi GV</pubmed_authors><pubmed_authors>Verderio P</pubmed_authors><pubmed_authors>Dugo M</pubmed_authors><pubmed_authors>Cleris L</pubmed_authors><pubmed_authors>Daidone MG</pubmed_authors><pubmed_authors>Cappelletti V</pubmed_authors><pubmed_authors>Lecis D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gene signatures of circulating breast cancer cell models are a source of novel molecular determinants of metastasis and improve circulating tumor cell detection in patients.</name><description>&lt;h4>Background&lt;/h4>Progression to stage IV disease remains the main cause of breast cancer-related deaths. Increasing knowledge on the hematogenous phase of metastasis is key for exploiting the entire window of opportunity to interfere with early dissemination and to achieve a more effective disease control. Recent evidence suggests that circulating tumor cells (CTCs) possess diverse adaptive mechanisms to survive in blood and eventually metastasize, encouraging research into CTC-directed therapies.&lt;h4>Methods&lt;/h4>On the hypothesis that the distinguishing molecular features of CTCs reveal useful information on metastasis biology and disease outcome, we compared the transcriptome of CTCs, primary tumors, lymph-node and lung metastases of the MDA-MB-231 xenograft model, and assessed the biol</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2026-04-08T17:21:32.859Z</modification><creation>2025-04-04T23:29:46.378Z</creation></dates><accession>S-EPMC8876758</accession><cross_references><pubmed>35216615</pubmed><doi>10.1186/s13046-022-02259-8</doi></cross_references></HashMap>