<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Califano D</submitter><funding>University of Campania "Luigi Vanvitelli"</funding><funding>Ministero della Salute</funding><funding>Ministero degli Affari Esteri</funding><funding>University of Campania &amp;quot;Luigi Vanvitelli&amp;quot;</funding><funding>Italian Association for Cancer Research</funding><funding>Associazione Italiana Di Oncologia Medica</funding><pagination>5152</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8533892</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(20)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Epithelial ovarian cancer (EOC) is a rare, highly lethal disease. In a subset of high grade EOC patients, maintenance therapy with the antiangiogenic drug Bevacizumab (BEV) is a valuable option. To date, no validated predictive or prognostic biomarkers exist for selecting EOC patients that might benefit from BEV treatment.&lt;h4>Methods&lt;/h4>Immunohistochemistry and RT-qPCR evaluated the expression of seven angiogenesis-related proteins and of a twelve microRNAs angio-signature in EOC patients, treated in first line with chemotherapy plus BEV (MITO16A/ManGO OV-2 phase IV trial). Centralized statistical analyses assessed the associations between each biomarker, clinical prognostic factors and survival outcomes.&lt;h4>Results&lt;/h4>High miR-484 expression was associated with longer</pubmed_abstract><journal>Cancers</journal><pubmed_title>Evaluation of Angiogenesis-Related Genes as Prognostic Biomarkers of Bevacizumab Treated Ovarian Cancer Patients: Results from the Phase IV MITO16A/ManGO OV-2 Translational Study.</pubmed_title><pmcid>PMC8533892</pmcid><funding_grant_id>To S.P.</funding_grant_id><funding_grant_id>CRO Ricerca Corrente grant (linea 1)</funding_grant_id><funding_grant_id>RCR-2019-23669115</funding_grant_id><funding_grant_id>PGR01230</funding_grant_id><funding_grant_id>IRCCS-G. Pascale Ricerca Corrente grant M2/7</funding_grant_id><funding_grant_id>Programma VALERE</funding_grant_id><funding_grant_id>20902</funding_grant_id><funding_grant_id>RF-2016-02361040</funding_grant_id><pubmed_authors>Russo D</pubmed_authors><pubmed_authors>Citron F</pubmed_authors><pubmed_authors>Perrone F</pubmed_authors><pubmed_authors>Montella M</pubmed_authors><pubmed_authors>Bignotti E</pubmed_authors><pubmed_authors>Gargiulo P</pubmed_authors><pubmed_authors>Zannoni GF</pubmed_authors><pubmed_authors>Signoriello S</pubmed_authors><pubmed_authors>Chiodini P</pubmed_authors><pubmed_authors>Simeon V</pubmed_authors><pubmed_authors>Scambia G</pubmed_authors><pubmed_authors>Losito NS</pubmed_authors><pubmed_authors>Baldassarre G</pubmed_authors><pubmed_authors>Scognamiglio G</pubmed_authors><pubmed_authors>Gallo D</pubmed_authors><pubmed_authors>De Cecio R</pubmed_authors><pubmed_authors>Spina A</pubmed_authors><pubmed_authors>Canzonieri V</pubmed_authors><pubmed_authors>Rampioni Vinciguerra GL</pubmed_authors><pubmed_authors>Pignata S</pubmed_authors><pubmed_authors>Cecere SC</pubmed_authors><pubmed_authors>Schettino C</pubmed_authors><pubmed_authors>Ferrandina G</pubmed_authors><pubmed_authors>Piccirillo MC</pubmed_authors><pubmed_authors>Tognon G</pubmed_authors><pubmed_authors>Del Sesto M</pubmed_authors><pubmed_authors>Califano D</pubmed_authors><pubmed_authors>Arenare L</pubmed_authors><pubmed_authors>Colombo N</pubmed_authors><pubmed_authors>Ciucci A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evaluation of Angiogenesis-Related Genes as Prognostic Biomarkers of Bevacizumab Treated Ovarian Cancer Patients: Results from the Phase IV MITO16A/ManGO OV-2 Translational Study.</name><description>&lt;h4>Background&lt;/h4>Epithelial ovarian cancer (EOC) is a rare, highly lethal disease. In a subset of high grade EOC patients, maintenance therapy with the antiangiogenic drug Bevacizumab (BEV) is a valuable option. To date, no validated predictive or prognostic biomarkers exist for selecting EOC patients that might benefit from BEV treatment.&lt;h4>Methods&lt;/h4>Immunohistochemistry and RT-qPCR evaluated the expression of seven angiogenesis-related proteins and of a twelve microRNAs angio-signature in EOC patients, treated in first line with chemotherapy plus BEV (MITO16A/ManGO OV-2 phase IV trial). Centralized statistical analyses assessed the associations between each biomarker, clinical prognostic factors and survival outcomes.&lt;h4>Results&lt;/h4>High miR-484 expression was associated with longer</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-04-08T06:49:01.614Z</modification><creation>2025-02-19T03:53:15.16Z</creation></dates><accession>S-EPMC8533892</accession><cross_references><pubmed>34680301</pubmed><doi>10.3390/cancers13205152</doi></cross_references></HashMap>