首页> 外文期刊>Medical and Pediatric Oncology: The Official Journal of the American Association for Cancer Education >Concentration of vascular endothelial growth factor (VEGF) in the serum of patients with malignant bone tumors.
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Concentration of vascular endothelial growth factor (VEGF) in the serum of patients with malignant bone tumors.

机译:恶性骨肿瘤患者血清中的血管内皮生长因子(VEGF)浓度。

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BACKGROUND: 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. PROCEDURE: 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). RESULTS: 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. CONCLUSIONS: 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. Copyright 2001 Wiley-Liss, Inc.
机译:背景:血管内皮生长因子(VEGF)被认为是重要的血管生成刺激剂。由血管生成因子形成的新血管发生在许多生理过程和病理过程中,包括原发性实体恶性肿瘤的生长和转移。这暗示着对血管生成因子如VEGF的抑制将导致肿瘤生长和转移形成的抑制。本研究的目的是将恶性骨肿瘤患者的术前血清VEGF水平与健康对照进行比较,以鉴定血清VEGF水平为肿瘤标志物。程序:在活检前确诊时采集了高度骨肉瘤(n = 17),软骨肉瘤(n = 4)和尤因肉瘤(n = 6)患者的血液血清,并将其与129名健康人的血清进行比较。为了测量血清中的VEGF水平,使用了市售的ELISA(Quantikine人VEGF免疫测定; R&D Systems)。结果:高级骨肉瘤患者的几何平均VEGF水平和95%置信区间为232.0 pg ml(-1)(168.9-318.5),软骨肉瘤患者为325.5 pg ml(-1)(169.3-625.8) ,尤因肉瘤患者为484.3 pg ml(-1)(284.0-826.0),健康个体为216.2 pg ml(-1)(192.8-242.5)。结论:尽管三组肉瘤患者的样本均值高于健康对照组的均值,但只有尤因肉瘤组的均值在统计学上显着高于健康对照组的均值。尽管有显着差异,但VEGF水平不适合用作尤因肉瘤的标志物。版权所有2001 Wiley-Liss,Inc.

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