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Prognostic value of serum angiogenic activity in colorectal cancer patients
Angiogenesis, resulting from an imbalance between angiogenic activator factors and inhibitors, is required for tumour growth and metastasis. The determination of the circulating concentration of all angiogenic factors (activators and inhibitors) is not feasible at present. We have evaluated diagnost...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401225/ https://www.ncbi.nlm.nih.gov/pubmed/17367506 http://dx.doi.org/10.1111/j.1582-4934.2007.00005.x |
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author | Gonzalez, Francisco-Jesus Quesada, Ana-Rodriguez Sevilla, Isabel Baca, Juan-Javier Medina, Miguel-Angel Amores, Jose Diaz, Juan Miguel Rius-Diaz, Francisca Marques, Eduardo Alba, Emilio |
author_facet | Gonzalez, Francisco-Jesus Quesada, Ana-Rodriguez Sevilla, Isabel Baca, Juan-Javier Medina, Miguel-Angel Amores, Jose Diaz, Juan Miguel Rius-Diaz, Francisca Marques, Eduardo Alba, Emilio |
author_sort | Gonzalez, Francisco-Jesus |
collection | PubMed |
description | Angiogenesis, resulting from an imbalance between angiogenic activator factors and inhibitors, is required for tumour growth and metastasis. The determination of the circulating concentration of all angiogenic factors (activators and inhibitors) is not feasible at present. We have evaluated diagnostic and prognostic values of the measurement of serum angiogenic activity in colorectal carcinoma (CRC) patients. Serum proliferative activity (PA) on human umbilical vein endothelial cells (HUVEC) in vitro, and serum vascular endothelial growth factor (VEGF) levels were determined by ELISA in 53 patients with primary CRC, 16 subjects with non-neoplastic gastrointestinal disease (SC) and 34 healthy individuals. Data were compared with clinical outcome of the patients. Although serum from CRC patients significantly increased the PA of HUVEC, compared to culture control (HUVEC in medium + 10% foetal bovine serum (FBS); P < 0.001); our results indicate that serum PA in CRC patients was similar to that of SC or healthy individuals. There was no correlation between serum PA and circulating VEGF concentrations. Surgery produced a decrease of PA at 8 hrs after tumour resection in CRC patients compared to pre-surgery values (186 ± 47 versus 213 ± 41, P < 0.001). However, an increase in serum VEGF values was observed after surgery (280 [176–450] versus 251 [160–357] pg/ml, P = 0.004). Patients with lower PA values after surgery showed a worse outcome that those with higher PA values. Therefore, this study does not support a diagnostic value for serum angiogenic activity measured by proliferative activity on HUVEC but suggests it could have a prognostic value in CRC patients. |
format | Online Article Text |
id | pubmed-4401225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44012252015-04-27 Prognostic value of serum angiogenic activity in colorectal cancer patients Gonzalez, Francisco-Jesus Quesada, Ana-Rodriguez Sevilla, Isabel Baca, Juan-Javier Medina, Miguel-Angel Amores, Jose Diaz, Juan Miguel Rius-Diaz, Francisca Marques, Eduardo Alba, Emilio J Cell Mol Med Articles Angiogenesis, resulting from an imbalance between angiogenic activator factors and inhibitors, is required for tumour growth and metastasis. The determination of the circulating concentration of all angiogenic factors (activators and inhibitors) is not feasible at present. We have evaluated diagnostic and prognostic values of the measurement of serum angiogenic activity in colorectal carcinoma (CRC) patients. Serum proliferative activity (PA) on human umbilical vein endothelial cells (HUVEC) in vitro, and serum vascular endothelial growth factor (VEGF) levels were determined by ELISA in 53 patients with primary CRC, 16 subjects with non-neoplastic gastrointestinal disease (SC) and 34 healthy individuals. Data were compared with clinical outcome of the patients. Although serum from CRC patients significantly increased the PA of HUVEC, compared to culture control (HUVEC in medium + 10% foetal bovine serum (FBS); P < 0.001); our results indicate that serum PA in CRC patients was similar to that of SC or healthy individuals. There was no correlation between serum PA and circulating VEGF concentrations. Surgery produced a decrease of PA at 8 hrs after tumour resection in CRC patients compared to pre-surgery values (186 ± 47 versus 213 ± 41, P < 0.001). However, an increase in serum VEGF values was observed after surgery (280 [176–450] versus 251 [160–357] pg/ml, P = 0.004). Patients with lower PA values after surgery showed a worse outcome that those with higher PA values. Therefore, this study does not support a diagnostic value for serum angiogenic activity measured by proliferative activity on HUVEC but suggests it could have a prognostic value in CRC patients. Blackwell Publishing Ltd 2007-01 2007-03-15 /pmc/articles/PMC4401225/ /pubmed/17367506 http://dx.doi.org/10.1111/j.1582-4934.2007.00005.x Text en |
spellingShingle | Articles Gonzalez, Francisco-Jesus Quesada, Ana-Rodriguez Sevilla, Isabel Baca, Juan-Javier Medina, Miguel-Angel Amores, Jose Diaz, Juan Miguel Rius-Diaz, Francisca Marques, Eduardo Alba, Emilio Prognostic value of serum angiogenic activity in colorectal cancer patients |
title | Prognostic value of serum angiogenic activity in colorectal cancer patients |
title_full | Prognostic value of serum angiogenic activity in colorectal cancer patients |
title_fullStr | Prognostic value of serum angiogenic activity in colorectal cancer patients |
title_full_unstemmed | Prognostic value of serum angiogenic activity in colorectal cancer patients |
title_short | Prognostic value of serum angiogenic activity in colorectal cancer patients |
title_sort | prognostic value of serum angiogenic activity in colorectal cancer patients |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401225/ https://www.ncbi.nlm.nih.gov/pubmed/17367506 http://dx.doi.org/10.1111/j.1582-4934.2007.00005.x |
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