Serum levels of vascular endothelial growth factor dependent on the stage progression of lung cancer

Citation
W. Matsuyama et al., Serum levels of vascular endothelial growth factor dependent on the stage progression of lung cancer, CHEST, 118(4), 2000, pp. 948-951
Citations number
19
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
CHEST
ISSN journal
00123692 → ACNP
Volume
118
Issue
4
Year of publication
2000
Pages
948 - 951
Database
ISI
SICI code
0012-3692(200010)118:4<948:SLOVEG>2.0.ZU;2-Z
Abstract
Study objective: In lung cancer, vascular endothelial growth factor (VEGF) is an important cytokine and is correlated with tumor vessel density, malig nant pleural effusions, and coagulation-fibrinolysis factors in vitro. We i nvestigated the correlation between serum VEGF level and stage progression in lung cancer to study the predicted value of VEGF level. We also studied whether coagulation-fibrinolysis factors and Pao(2) levels, which are also important factors for the prediction of the clinical course, are correlated with VEGF. Methods: Forty-nine patients with lung cancer were investigated prospective ly. VEGF levels of sera and malignant effusions, and plasma concentrations of coagulation-fibrinolysis factors were measured by enzyme-linked immunoso rbent assay. We measured Pao(2) levels in all patients at rest. Results: Serum levels of VEGF were increased significantly according to sta ge progression. Additionally, plasma concentrations of D dimer, thrombin-an tithrombin complex (TAT), and tissue plasminogen activator/plasminogen acti vator inhibitor type I complex were elevated significantly according to sta ge progression. The serum VEGF level had a significant positive correlation with the TAT and D dimer levels. Serum VEGF levels had a significant negat ive correlation with Pao(2) levels. The incidence of cerebral vascular diso rder was significantly higher in the patients with systemic hypoxemia than in those without (p < 0.05). Mean VEGF levels in malignant effusions in eig ht patients (five with pleural effusions, two with pericardial effusions, a nd one with both) were extremely high, especially in pericardial effusions ([mean +/- SD] pleural effusions, 531.9 +/- 285.4 pg/mL; pericardial effusi on, 3,071.6 +/- 81.3 pg/mL). Conclusion: We predict that in lung cancer, VEGF production and the abnorma lity of the congulation-fibrinolysis system differ depending on the stage o f progression of disease. Serum VEGF levels would be affected by Pao(2) lev els in lung cancer.