Holzer G, Obermair A, Koschat M, Preyer O, Kotz R, Trieb K
Department of Orthopaedics, University of Vienna, Vienna General Hospital, Vienna, Austria.
Med Pediatr Oncol. 2001 Jun;36(6):601-4. doi: 10.1002/mpo.1136.
Vascular endothelial growth factor (VEGF) is recognized as an important stimulator of angiogenesis. Formation of new blood vessels by angiogenic factors occurs in many biological processes, both physiological and pathological, among others in growth of primary solid malignant tumors and metastasis. This implies that the inhibition of angiogenic factors like VEGF would result in a suppression of tumor growth and metastasis formation. The aim of the present study was to compare preoperative serum VEGF levels of patients having malignant bone tumors with healthy controls to identify serum VEGF levels as a tumor marker.
Blood sera from patients with high-grade osteosarcoma (n = 17), chondrosarcoma (n = 4) and Ewing sarcoma (n = 6) were taken at the time of diagnosis before biopsy and compared with sera from 129 healthy persons. To measure VEGF levels in serum, a commercially available ELISA was used (Quantikine Human VEGF Immunoassay; R&D Systems).
The observed geometric mean VEGF levels and 95% confidence intervals are 232.0 pg ml(-1) (168.9-318.5) for patients with high-grade osteosarcoma, 325.5 pg ml(-1) (169.3-625.8) for patients with chondrosarcoma, 484.3 pg ml(-1) (284.0-826.0) for patients with Ewing sarcoma, as compared to 216.2 pg ml(-1) (192.8-242.5) for healthy individuals.
While the sample means for the three groups of sarcoma patients were higher than the respective mean for the healthy controls, only the mean for the group with Ewing sarcoma is statistically significantly higher than the mean for the healthy controls. Despite the significant difference, VEGF levels are not suitable as a marker for Ewing sarcoma.
血管内皮生长因子(VEGF)被认为是血管生成的重要刺激因子。血管生成因子介导的新血管形成发生在许多生理和病理生物学过程中,包括原发性实体恶性肿瘤的生长和转移。这意味着抑制像VEGF这样的血管生成因子会导致肿瘤生长和转移形成受到抑制。本研究的目的是比较恶性骨肿瘤患者与健康对照者术前血清VEGF水平,以确定血清VEGF水平作为肿瘤标志物。
在诊断时活检前采集17例高级别骨肉瘤、4例软骨肉瘤和6例尤因肉瘤患者的血清,并与129名健康人的血清进行比较。使用市售的酶联免疫吸附测定法(Quantikine Human VEGF Immunoassay;R&D Systems)测量血清中的VEGF水平。
高级别骨肉瘤患者观察到的VEGF几何平均水平和95%置信区间为232.0 pg/ml(168.9 - 318.5),软骨肉瘤患者为325.5 pg/ml(169.3 - 625.8),尤因肉瘤患者为484.3 pg/ml(284.0 - 826.0),而健康个体为216.2 pg/ml(192.8 - 242.5)。
虽然三组肉瘤患者的样本均值高于健康对照者各自的均值,但只有尤因肉瘤组的均值在统计学上显著高于健康对照者的均值。尽管存在显著差异,但VEGF水平不适宜作为尤因肉瘤的标志物。