<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pajares MJ</submitter><funding>NCI NIH HHS</funding><pagination>1129-36</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4874209</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(10)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Antiangiogenic therapies targeting the vascular endothelial growth factor (VEGF) pathway have yielded more modest clinical benefit to patients with non-small-cell lung cancer (NSCLC) than initially expected. Clinical data suggest a distinct biologic role of the VEGF pathway in the different histologic subtypes of lung cancer. To clarify the influence of histologic differentiation in the prognostic relevance of VEGF-mediated signaling in NSCLC, we performed a concomitant analysis of the expression of three key elements of the VEGF pathway in the earliest stages of the following two principal histologic subtypes: squamous cell carcinoma (SCC) and adenocarcinoma (ADC).&lt;h4>Patients and methods&lt;/h4>We evaluated tumor cell expression of VEGF, VEGF receptor (VEGFR) 1, and VEGFR2 u</pubmed_abstract><journal>Journal of clinical oncology : official journal of the American Society of Clinical Oncology</journal><pubmed_title>Expression of tumor-derived vascular endothelial growth factor and its receptors is associated with outcome in early squamous cell carcinoma of the lung.</pubmed_title><pmcid>PMC4874209</pmcid><funding_grant_id>P50 CA070907</funding_grant_id><funding_grant_id>P30 CA016672</funding_grant_id><pubmed_authors>Pajares MJ</pubmed_authors><pubmed_authors>Montuenga LM</pubmed_authors><pubmed_authors>Wistuba II</pubmed_authors><pubmed_authors>Zudaire I</pubmed_authors><pubmed_authors>Timsit JF</pubmed_authors><pubmed_authors>Ezponda T</pubmed_authors><pubmed_authors>Brambilla C</pubmed_authors><pubmed_authors>Larrayoz M</pubmed_authors><pubmed_authors>Behrens C</pubmed_authors><pubmed_authors>Brambilla E</pubmed_authors><pubmed_authors>Torre W</pubmed_authors><pubmed_authors>Pio R</pubmed_authors><pubmed_authors>Agorreta J</pubmed_authors><pubmed_authors>Vesin A</pubmed_authors><pubmed_authors>Lozano MD</pubmed_authors><pubmed_authors>Field JK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Expression of tumor-derived vascular endothelial growth factor and its receptors is associated with outcome in early squamous cell carcinoma of the lung.</name><description>&lt;h4>Purpose&lt;/h4>Antiangiogenic therapies targeting the vascular endothelial growth factor (VEGF) pathway have yielded more modest clinical benefit to patients with non-small-cell lung cancer (NSCLC) than initially expected. Clinical data suggest a distinct biologic role of the VEGF pathway in the different histologic subtypes of lung cancer. To clarify the influence of histologic differentiation in the prognostic relevance of VEGF-mediated signaling in NSCLC, we performed a concomitant analysis of the expression of three key elements of the VEGF pathway in the earliest stages of the following two principal histologic subtypes: squamous cell carcinoma (SCC) and adenocarcinoma (ADC).&lt;h4>Patients and methods&lt;/h4>We evaluated tumor cell expression of VEGF, VEGF receptor (VEGFR) 1, and VEGFR2 u</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Apr</publication><modification>2026-06-04T15:34:02.835Z</modification><creation>2019-03-27T02:14:11Z</creation></dates><accession>S-EPMC4874209</accession><cross_references><pubmed>22355056</pubmed><doi>10.1200/JCO.2011.37.4231</doi><doi>10.1200/jco.2011.37.4231</doi></cross_references></HashMap>