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PMID: 9815646 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Are angiogenic factors, cytokines, and soluble adhesion molecules prognostic factors in patients with renal cell carcinoma?

Dosquet C, Coudert MC, Lepage E, Cabane J, Richard F

Abstract

Angiogenesis has an important role in the progression of solid tumors. Therefore, we measured the blood levels (ELISA) of angiogenic factors [basic fibroblast growth factor (bFGF), hepatocyte growth factor/scatter factor, and vascular endothelial growth factor (VEGF)] and soluble adhesion molecules [E-selectin, intercellular adhesion molecule (ICAM-1), platelet endothelial cell adhesion molecule-1, and vascular cell adhesion molecule-1] in 76 consecutive patients with untreated renal cell carcinoma and 41 healthy controls to evaluate their prognostic value. The serum levels of bFGF, hepatocyte growth factor, and VEGF were significantly higher in patients with renal cancer than they were in healthy subjects. bFGF and VEGF values were significantly higher in patients with disseminated cancer (N+ and/or M+) than they were in those with undisseminated (M-N-) cancer: median = 27 pg/ml, range = 5-118, n = 15 versus median = 8 pg/ml, range = 1-149, n = 61 (P = 10(-4)) for bFGF; and median = 883 pg/ml, range = 200-2317, n = 15 versus median = 278 pg/ml, range = 0-1704, n = 61 (P = 0.006) for VEGF. The blood levels of ICAM-1 and vascular cell adhesion molecule-1 were significantly higher, and the levels of E-selectin and platelet endothelial cell adhesion molecule-1 were significantly lower in patients with renal cancer than they were in controls. Plasma ICAM-1 was higher in metastatic patients (M+) than they were in nonmetastatic (M-) patients: median = 687 ng/ml, range = 294-1091, n = 12 versus median = 408 ng/ml, range = 217-1375, n = 64 (P = 10(-4)). ICAM-1 and bFGF blood values were correlated with the size of the primary tumor. The interleukin 6 and tumor necrosis factor-alpha (TNF-alpha) values of these patients have been previously published and are included in the survival analysis. Univariate analysis showed that bFGF, ICAM-1, interleukin 6, and TNF-alpha, before treatment, were prognostic factors. In multivariate analysis for proportional hazard regression, only TNF-alpha was an independent prognostic indicator, with a normal plasma TNF-alpha being highly predictive for a good prognosis in patients with untreated renal cell carcinoma.

MeSH Terms
Adult Aged Aged, 80 and over Biomarkers, Tumor/blood Carcinoma, Renal Cell/blood,mortality,pathology,surgery Cell Adhesion Molecules/blood Cytokines/blood E-Selectin/blood Endothelial Growth Factors/blood Female Fibroblast Growth Factor 2/blood Hepatocyte Growth Factor/blood Humans Intercellular Adhesion Molecule-1/blood Interleukin-6/blood Kidney Neoplasms/blood,mortality,pathology,surgery Lymphatic Metastasis Lymphokines/blood Male Middle Aged Neoplasm Metastasis Neoplasm Staging Platelet Endothelial Cell Adhesion Molecule-1/blood Predictive Value of Tests Prognosis Reference Values Survival Analysis Time Factors Tumor Necrosis Factor-alpha/analysis Vascular Cell Adhesion Molecule-1/blood Vascular Endothelial Growth Factor A Vascular Endothelial Growth Factors
Chemicals
Biomarkers, Tumor Cell Adhesion Molecules Cytokines E-Selectin Endothelial Growth Factors Interleukin-6 Lymphokines Platelet Endothelial Cell Adhesion Molecule-1 Tumor Necrosis Factor-alpha Vascular Cell Adhesion Molecule-1 Vascular Endothelial Growth Factor A Vascular Endothelial Growth Factors Fibroblast Growth Factor 2 Intercellular Adhesion Molecule-1 Hepatocyte Growth Factor
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Dosquet C
Centre de Transfusion, Laboratoire des Cytokines, Hôpital Saint-Louis, 75475 Paris Cedex 10, France.
Coudert M C
Lepage E
Cabane J
Richard F
Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1078-0432
Published
1997-12-00
Pages
2451-8
Language
English
Region
United States
NLM ID
9502500
Subset
IM
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