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Plasma levels of vascular endothelial growth factor are increased in patients with metastatic prostate cancer.

机译:转移性前列腺癌患者的血浆血管内皮生长因子水平升高。

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OBJECTIVES: Vascular endothelial growth factor (VEGF) is a cytokine that plays an important role in tumor angiogenesis. VEGF is overexpressed in many human cancers, including prostate cancer, but circulating levels of VEGF in patients with prostate cancer have not been reported. In this study, we analyzed plasma concentrations of VEGF in a cohort of patients with prostate cancer and compared them with a normal population. METHODS: Twenty-six healthy, cancer-free individuals and 80 patients with prostate cancer (54 patients with localized prostate cancer and 26 patients with metastatic prostate cancer [bone or lymph node positive]) were analyzed in this study. Blood was drawn in the same fashion from all individuals and deposited in tubes containing ethylenediaminetetraacetic acid as anticoagulant. Plasma was extracted and VEGF concentrations were determined using a quantitative sandwich enzyme immunoassay technique. RESULTS: Median plasma VEGF was 28.5 pg/mL (interquartile range 19.3 to 57.0) in patients with metastases; 7.0 pg/mL (interquartile range 0 to 26.5) in patients with localized disease, and 0 pg/mL (interquartile range 0 to 24) in controls. These differences were statistically significant (P <0.001). When compared group by group, the metastatic group had significantly higher plasma VEGF than the localized disease group and the control group (P = 0.003 and P <0.001, respectively). There was a tendency for plasma VEGF to be higher in the localized disease group than in the control group, a trend that almost reached statistical significance (P = 0.038). Using a cutoff of 18 pg/mL, the sensitivity and specificity of the test in differentiating between patients with and without metastatic disease was 81% and 71%, respectively. The odds of metastatic disease were almost 10 times greater for patients with VEGF values greater than 18 pg/mL than for those with values less than 18 pg/mL. There was no correlation between age and plasma VEGF values or between plasma VEGF and serum prostate-specific antigen (PSA). However, patients with serum PSA greater than 20 ng/mL had significantly higher plasma VEGF values than patients with serum PSA less than 20 ng/mL (P <0.001). No direct relation was found between Gleason sum and plasma VEGF, although VEGF levels were higher in patients with Gleason sums of 8 to 10 than in patients with lower Gleason sums. CONCLUSIONS: Our study indicates that patients with metastatic prostate cancer have higher plasma VEGF levels than patients with localized disease or healthy controls. A larger prospective study is needed to confirm the predictive utility of VEGF.
机译:目的:血管内皮生长因子(VEGF)是一种在肿瘤血管生成中起重要作用的细胞因子。 VEGF在包括前列腺癌在内的许多人类癌症中过表达,但尚未报道前列腺癌患者体内VEGF的循环水平。在这项研究中,我们分析了前列腺癌患者队列中的VEGF血浆浓度,并将其与正常人群进行了比较。方法:本研究分析了26名健康,无癌的个体和80例前列腺癌患者(54例局部前列腺癌患者和26例转移性前列腺癌患者(骨或淋巴结阳性))。从所有个体以相同方式抽取血液,并将其沉积在含有乙二胺四乙酸作为抗凝剂的试管中。提取血浆并使用定量夹心酶免疫测定技术测定VEGF浓度。结果:转移患者中血浆VEGF的中位数为28.5 pg / mL(四分位数范围为19.3至57.0)。局部疾病患者为7.0 pg / mL(四分位范围0至26.5),对照组为0 pg / mL(四分位范围0至24)。这些差异具有统计学意义(P <0.001)。当逐组比较时,转移组的血浆VEGF明显高于局部疾病组和对照组(分别为P = 0.003和P <0.001)。在局部疾病组中血浆VEGF有高于对照组的趋势,这一趋势几乎达到统计学显着性(P = 0.038)。使用18 pg / mL的临界值,该测试在区分是否患有转移性疾病的患者中的敏感性和特异性分别为81%和71%。 VEGF值大于18 pg / mL的患者的转移性疾病几率比值小于18 pg / mL的患者高10倍。年龄与血浆VEGF值之间或血浆VEGF与血清前列腺特异性抗原(PSA)之间没有相关性。但是,血清PSA大于20 ng / mL的患者血浆VEGF值明显高于血清PSA小于20 ng / mL的患者(P <0.001)。格里森和与血浆VEGF之间没有直接关系,尽管格里森和为8至10的患者的VEGF水平高于格里森和为较低的患者。结论:我们的研究表明转移性前列腺癌患者血浆VEGF水平高于局部疾病或健康对照者。需要进行更大规模的前瞻性研究来证实VEGF的预测效用。

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