Serum vascular endothelial growth factor per platelet count in hepatocellular carcinoma: Correlations with clinical parameters and survival

被引:50
作者
Kim, SJ [1 ]
Choi, IK [1 ]
Park, KH [1 ]
Yoon, SY [1 ]
Oh, SC [1 ]
Seo, JH [1 ]
Choi, CW [1 ]
Kim, BS [1 ]
Shin, SW [1 ]
Kim, YH [1 ]
Kim, JS [1 ]
机构
[1] Korea Univ, Med Ctr, Div Hematol & Oncol, Dept Internal Med,Anam Hosp, Seoul 136705, South Korea
关键词
hepatocellular carcinoma (HCC); platelet count; vascular endothelial growth factor;
D O I
10.1093/jjco/hyh039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Platelets have been reported to act as transporters of tumor-originated vascular endothelial growth factor (VEGF), contributing to tumor angiogenesis and progression. Serum VEGF per platelet count, as an indirect theoretical estimate of VEGF in platelets, may predict the malignant potential of tumors. However, its prognostic significance is still unclear in hepatocellular carcinoma (HCC), a highly vascular tumor. Methods: Serum VEGF was measured by enzyme-linked immunosorbent assay. We compared serum VEGF, platelet count and serum VEGF per platelet count in 52 HCC patients, 26 liver cirrhosis patients and 30 healthy controls. The relation of serum VEGF per platelet count with clinicopathologic variables of HCC patients and the prognostic significance were investigated. Results: Serum VEGF per platelet count in HCC patients was higher than in liver cirrhosis patients and healthy controls (P < 0.01). There was a statistically significant correlation between serum VEGF and platelet count in HCC patients (r = 0.751, P < 0.01). Serum VEGIF per platelet count was higher in patients with advanced stage and portal vein thrombosis (P < 0.01). Patients with high serum VEGF per platelet count ( > 1.4 pg/10(6)) showed poor response to treatment and shorter overall survival (P < 0.01). Serum VEGF per platelet count was an independent prognostic factor with the presence of portal vein thrombosis (P < 0.01). Conclusions: Serum VEGF per platelet count could be a feasible prognostic indicator during the follow-up of patients with HCC.
引用
收藏
页码:184 / 190
页数:7
相关论文
共 25 条
[1]   Prognostic role of serum vascular endothelial growth factor, basic fibroblast growth factor and nitric oxide in patients with colorectal carcinoma [J].
Akbulut, H ;
Altuntas, F ;
Akbulut, KG ;
Ozturk, G ;
Cindoruk, M ;
Unal, E ;
Icli, F .
CYTOKINE, 2002, 20 (04) :184-190
[2]   Association of vascular endothelial growth factor expression with tumor angiogenesis, survival and thymidine phosphorylase/platelet-derived endothelial cell growth factor expression in human colorectal cancer [J].
Amaya, H ;
Tanigawa, N ;
Lu, C ;
Matsumura, M ;
Shimomatsuya, T ;
Horiuchi, T ;
Muraoka, R .
CANCER LETTERS, 1997, 119 (02) :227-235
[3]   Release of the angiogenic cytokine vascular endothelial growth factor (VEGF) from platelets: significance for VEGF measurements and cancer biology [J].
Banks, RE ;
Forbes, MA ;
Kinsey, SE ;
Stanley, A ;
Ingham, E ;
Walters, C ;
Selby, PJ .
BRITISH JOURNAL OF CANCER, 1998, 77 (06) :956-964
[4]  
Benoy Ina, 2002, Clin Breast Cancer, V2, P311, DOI 10.3816/CBC.2002.n.008
[5]   Prognostic significance of platelet and microvessel counts in operable non-small cell lung cancer [J].
Cox, G ;
Walker, RA ;
Andi, A ;
Steward, WP ;
O'Byrne, KJ .
LUNG CANCER, 2000, 29 (03) :169-177
[6]  
DVORAK HF, 1995, AM J PATHOL, V146, P1029
[7]  
George ML, 2000, CLIN CANCER RES, V6, P3147
[8]   Thrombocytosis as a prognostic factor in endometrial carcinoma [J].
Gucer, F ;
Moser, F ;
Tamussino, K ;
Reich, O ;
Haas, J ;
Arikan, G ;
Petru, E ;
Winter, R .
GYNECOLOGIC ONCOLOGY, 1998, 70 (02) :210-214
[9]   INCORPORATION OF A CIRCULATING PROTEIN INTO MEGAKARYOCYTE AND PLATELET GRANULES [J].
HANDAGAMA, PJ ;
GEORGE, JN ;
SHUMAN, MA ;
MCEVER, RP ;
BAINTON, DF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (03) :861-865
[10]   UPTAKE OF PLASMA-FIBRINOGEN INTO THE ALPHA-GRANULES OF HUMAN MEGAKARYOCYTES AND PLATELETS [J].
HARRISON, P ;
WILBOURN, B ;
DEBILI, N ;
VAINCHENKER, W ;
BRETONGORIUS, J ;
LAWRIE, AS ;
MASSE, JM ;
SAVIDGE, GF ;
CRAMER, EM .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (04) :1320-1324