TIMP-1 and VEGF-165 serum concentration during first-line therapy of ovarian cancer patients

<p>Abstract</p> <p>Background</p> <p>Angiogenesis appears to play an important role in ovarian cancer. Vascular endothelial growth factor (VEGF) has recently been implicated as a therapeutic target in ovarian cancer. The tissue inhibitor of metalloproteinase 1 (TIMP-1)...

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Main Authors: Jaenicke Fritz, Carney Walter, Schwarz Joerg, Eulenburg Christine, Woelber Linn, Mahner Sven, Milde-Langosch Karin, Mueller Volkmar
Format: Article
Language:English
Published: BMC 2010-04-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/10/139
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author Jaenicke Fritz
Carney Walter
Schwarz Joerg
Eulenburg Christine
Woelber Linn
Mahner Sven
Milde-Langosch Karin
Mueller Volkmar
author_facet Jaenicke Fritz
Carney Walter
Schwarz Joerg
Eulenburg Christine
Woelber Linn
Mahner Sven
Milde-Langosch Karin
Mueller Volkmar
author_sort Jaenicke Fritz
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Angiogenesis appears to play an important role in ovarian cancer. Vascular endothelial growth factor (VEGF) has recently been implicated as a therapeutic target in ovarian cancer. The tissue inhibitor of metalloproteinase 1 (TIMP-1) is involved in tissue invasion and angiogenesis. The application of serum TIMP-1 and VEGF to monitor primary therapy and predict clinical outcome of patients with ovarian cancer is unclear.</p> <p>Methods</p> <p>Patients with epithelial ovarian cancer who presented for primary surgery were included in this study. A total of 148 serum samples from 37 patients were analyzed. Samples were prospectively collected at 4 predefined time points: 1. before radical debulking surgery, 2. after surgery and before platinum/taxane based chemotherapy, 3. during chemotherapy, 4. after chemotherapy. Serum VEGF-165 and TIMP-1 as well as CA-125 were quantified by ELISA or ECLIA and correlation with response and long-term clinical outcome was analyzed.</p> <p>Results</p> <p>Serum levels of all markers changed substantially during first-line therapy. High CA-125 (p = 0.002), TIMP-1 (p = 0.007) and VEGF-165 (p = 0.02) after chemotherapy were associated with reduced overall survival. In addition, elevated CA-125 (p < 0.001) and VEGF-165 (p = 0.006) at this time point predicted poor progression-free survival. TIMP-1 and VEGF-165 were closely correlated at all time-points during therapy.</p> <p>Conclusions</p> <p>TIMP-1 and VEGF serum levels changed significantly during first-line therapy of ovarian cancer patients and predicted prognosis. These findings support the role of angiogenesis in ovarian cancer progression and the use of antiangiogenic therapy.</p>
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spelling doaj.art-19e9be76147d49b0ac97269c8f3b898a2022-12-22T00:36:39ZengBMCBMC Cancer1471-24072010-04-0110113910.1186/1471-2407-10-139TIMP-1 and VEGF-165 serum concentration during first-line therapy of ovarian cancer patientsJaenicke FritzCarney WalterSchwarz JoergEulenburg ChristineWoelber LinnMahner SvenMilde-Langosch KarinMueller Volkmar<p>Abstract</p> <p>Background</p> <p>Angiogenesis appears to play an important role in ovarian cancer. Vascular endothelial growth factor (VEGF) has recently been implicated as a therapeutic target in ovarian cancer. The tissue inhibitor of metalloproteinase 1 (TIMP-1) is involved in tissue invasion and angiogenesis. The application of serum TIMP-1 and VEGF to monitor primary therapy and predict clinical outcome of patients with ovarian cancer is unclear.</p> <p>Methods</p> <p>Patients with epithelial ovarian cancer who presented for primary surgery were included in this study. A total of 148 serum samples from 37 patients were analyzed. Samples were prospectively collected at 4 predefined time points: 1. before radical debulking surgery, 2. after surgery and before platinum/taxane based chemotherapy, 3. during chemotherapy, 4. after chemotherapy. Serum VEGF-165 and TIMP-1 as well as CA-125 were quantified by ELISA or ECLIA and correlation with response and long-term clinical outcome was analyzed.</p> <p>Results</p> <p>Serum levels of all markers changed substantially during first-line therapy. High CA-125 (p = 0.002), TIMP-1 (p = 0.007) and VEGF-165 (p = 0.02) after chemotherapy were associated with reduced overall survival. In addition, elevated CA-125 (p < 0.001) and VEGF-165 (p = 0.006) at this time point predicted poor progression-free survival. TIMP-1 and VEGF-165 were closely correlated at all time-points during therapy.</p> <p>Conclusions</p> <p>TIMP-1 and VEGF serum levels changed significantly during first-line therapy of ovarian cancer patients and predicted prognosis. These findings support the role of angiogenesis in ovarian cancer progression and the use of antiangiogenic therapy.</p>http://www.biomedcentral.com/1471-2407/10/139
spellingShingle Jaenicke Fritz
Carney Walter
Schwarz Joerg
Eulenburg Christine
Woelber Linn
Mahner Sven
Milde-Langosch Karin
Mueller Volkmar
TIMP-1 and VEGF-165 serum concentration during first-line therapy of ovarian cancer patients
BMC Cancer
title TIMP-1 and VEGF-165 serum concentration during first-line therapy of ovarian cancer patients
title_full TIMP-1 and VEGF-165 serum concentration during first-line therapy of ovarian cancer patients
title_fullStr TIMP-1 and VEGF-165 serum concentration during first-line therapy of ovarian cancer patients
title_full_unstemmed TIMP-1 and VEGF-165 serum concentration during first-line therapy of ovarian cancer patients
title_short TIMP-1 and VEGF-165 serum concentration during first-line therapy of ovarian cancer patients
title_sort timp 1 and vegf 165 serum concentration during first line therapy of ovarian cancer patients
url http://www.biomedcentral.com/1471-2407/10/139
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