<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>103(9)</volume><submitter>Goede V</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The combination of chemotherapy with the vascular endothelial growth factor (VEGF) antibody bevacizumab is a standard of care in advanced colorectal cancer (CRC). However, biomarkers predicting outcome of bevacizumab-containing treatment are lacking. As angiopoietin-2 (Ang-2) is a key regulator of vascular remodelling in concert with VEGF, we investigated its role as a biomarker in metastatic CRC.&lt;h4>Methods&lt;/h4>Serum Ang-2 levels were measured in 33 healthy volunteers and 90 patients with CRC. Of these, 34 had metastatic disease and received bevacizumab-containing therapy. To determine the tissue of origin of Ang-2, quantitative real-time PCR was performed on microdissected cryosections of human CRC and in a murine xenograft model of CRC using species-specific amplifica</pubmed_abstract><journal>British journal of cancer</journal><pagination>1407-14</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2990609</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification of serum angiopoietin-2 as a biomarker for clinical outcome of colorectal cancer patients treated with bevacizumab-containing therapy.</pubmed_title><pmcid>PMC2990609</pmcid><pubmed_authors>Koslowsky TC</pubmed_authors><pubmed_authors>Schnell R</pubmed_authors><pubmed_authors>Coutelle O</pubmed_authors><pubmed_authors>Reinacher-Schick A</pubmed_authors><pubmed_authors>Hacker UT</pubmed_authors><pubmed_authors>Odenthal M</pubmed_authors><pubmed_authors>Schmiegel W</pubmed_authors><pubmed_authors>Neuneier J</pubmed_authors><pubmed_authors>Kashkar H</pubmed_authors><pubmed_authors>Hallek M</pubmed_authors><pubmed_authors>Weihrauch MR</pubmed_authors><pubmed_authors>Goede V</pubmed_authors><pubmed_authors>Cremer B</pubmed_authors><pubmed_authors>Augustin HG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of serum angiopoietin-2 as a biomarker for clinical outcome of colorectal cancer patients treated with bevacizumab-containing therapy.</name><description>&lt;h4>Background&lt;/h4>The combination of chemotherapy with the vascular endothelial growth factor (VEGF) antibody bevacizumab is a standard of care in advanced colorectal cancer (CRC). However, biomarkers predicting outcome of bevacizumab-containing treatment are lacking. As angiopoietin-2 (Ang-2) is a key regulator of vascular remodelling in concert with VEGF, we investigated its role as a biomarker in metastatic CRC.&lt;h4>Methods&lt;/h4>Serum Ang-2 levels were measured in 33 healthy volunteers and 90 patients with CRC. Of these, 34 had metastatic disease and received bevacizumab-containing therapy. To determine the tissue of origin of Ang-2, quantitative real-time PCR was performed on microdissected cryosections of human CRC and in a murine xenograft model of CRC using species-specific amplifica</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Oct</publication><modification>2025-04-04T19:42:35.42Z</modification><creation>2019-03-27T00:36:51Z</creation></dates><accession>S-EPMC2990609</accession><cross_references><pubmed>20924372</pubmed><doi>10.1038/sj.bjc.6605925</doi></cross_references></HashMap>