Serum levels of E-selectin, ICAM-1 and VCAM-1 in colorectal cancer patients: correlations with clinicopathological features, patient survival and tumour surgery

被引:151
作者
Alexiou, D
Karayiannakis, AJ [1 ]
Syrigos, KN
Zbar, A
Kremmyda, A
Bramis, I
Tsigris, C
机构
[1] Democritus Univ Thrace, Sch Med, Dept Surg 2, Alexandroupolis 68100, Greece
[2] Univ Athens, Sch Med, Dept Surg 1, GR-11527 Athens, Greece
[3] Univ Athens, Sch Med, Dept Med 3, GR-11527 Athens, Greece
[4] Kaplan Med Ctr, Dept Surg, IL-76100 Rehovot, Israel
关键词
cell adhesion molecule; E-selectin; ICAM-1; VCAM-1; surgery; prognosis; survival;
D O I
10.1016/S0959-8049(01)00318-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The serum concentrations oft he cell adhesion molecules E-select in, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) were investigated in 63 patients with colorectal cancer and in 51 controls by an enzyme-linked immunosorbent assay (ELISA). Their relationship to clinicopathological variables and patient survival and changes in their levels after surgery were examined. Colorectal cancer patients showed significantly higher serum levels of E-selectin, ICAM-1 and VCAM-1 compared with healthy controls. There was a significant association between. the serum levels of these molecules, disease stage and the presence of both lymph node and distant metastases. Both ICAM-1 and VCAM-1 levels correlated with serum E-selectin and carcinoembryonic antigen (CEA) levels. Serum levels of all three molecules decreased significantly after radical resection of the tumour. Elevated pre-operative E-selectin. ICAM-1 and VCAM-1 levels were significant prognostic factors, although not independent of stage. for patient survival. These findings suggest that serum concentrations of E-selectin, ICAM-1 and VCAM-1 may reflect tumour progression and metastasis. Since these markers are linked to CEA levels, it is uncertain whether their measurement will prove cost-effective in colorectal cancer management. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2392 / 2397
页数:6
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