Peng Xiao-ping, Li Jun-dong, Li Meng-da, Ye Xian-ming, Yan Wan-chang
Department of Gynaecology, Cancer Center, Sun Yat-sun University, Guangzhou 510060, P. R. China.
Ai Zheng. 2002 Feb;21(2):181-5.
BACKGROUND & OBJECTIVE: Experimental and clinical evidence links tumor growth, invasion, and metastatic potential with neoangiogenesis. This process is modulated by several angiogenic growth factors, such as vascular endothelial growth factor(VEGF). Few data are currently available on serum level in patients with gynaecological malignant tumors. This study was designed to determine the serum VEGF level in the patients with gynaecological malignant tumors and its significance as a tumor marker.
MATERIAL & METHODS: Preoperative serum VEGF level were measured in 50 cervical cancer, 39 endometrial cancer, 89 ovarian cancer patients, and 80 normal healthy women; The serum VEGF levels were also measured in 3, 6, 9 months after operation and when recurrence in three curative resection patients with ovarian cancer; using commercially available enzymelinked immonosarbent assay (R & D systems Inc. Minneapolis, MN, USA). Statistical analysis was performed by using the SPSS9.0 software package. Using 5th and 95th percentage describe the variant degree.
The median level of VEGF in sera of 80 healthy women was 218.50 ng/L(42.06-671.70 ng/L), while in 50 cervical cancer, 39 endometrial cancer, and 89 ovarian cancer patients were 272.00 ng/L(91.94-745.53 ng/L), 383.50 ng/L(105.67-776.50 ng/L), and 479.85 ng/L (99.47-1326.88 ng/L), respectively. The VEGF levels in endometrial cancer and ovarian cancer patients were significantly higher than that in healthy women (P < 0.0001). But in cervical cancer patients the VEGF level, was not significant diffent compare with health wanen. After operation, 3, 6, 9 months the VEGF levels in 3 ovarian cancer patients were significantly lower than that of preoperative but it ascended again when the disease was recurrent 14, 17 months later in two cases. The VEGF level was significantly higher in advanced ovarian cancer patients (stage III-IV) than that in the early stage (stage I-II) (P < 0.05).
The serum level of the VEGF may be used as a new tumor marker of endometrial cancer and ovarian cancer, for diagnoses and monitoring the progress of the disease.
实验和临床证据表明肿瘤生长、侵袭及转移潜能与新生血管形成有关。这一过程受多种血管生成生长因子调控,如血管内皮生长因子(VEGF)。目前关于妇科恶性肿瘤患者血清水平的数据较少。本研究旨在测定妇科恶性肿瘤患者血清VEGF水平及其作为肿瘤标志物的意义。
检测50例宫颈癌、39例子宫内膜癌、89例卵巢癌患者及80例正常健康女性术前血清VEGF水平;对3例卵巢癌根治性切除患者术后3、6、9个月及复发时的血清VEGF水平也进行了检测;采用美国明尼阿波利斯市R&D系统公司的商用酶联免疫吸附测定法。使用SPSS9.0软件包进行统计分析。用第5百分位数和第95百分位数描述变异程度。
80例健康女性血清VEGF中位数水平为218.50 ng/L(42.06 - 671.70 ng/L),而50例宫颈癌、39例子宫内膜癌及89例卵巢癌患者分别为272.00 ng/L(91.94 - 745.53 ng/L)、383.50 ng/L(105.67 - 776.50 ng/L)及479.85 ng/L(99.47 - 1326.88 ng/L)。子宫内膜癌和卵巢癌患者的VEGF水平显著高于健康女性(P < 0.0001)。但宫颈癌患者的VEGF水平与健康女性相比无显著差异。术后3、6、9个月,3例卵巢癌患者的VEGF水平显著低于术前,但在14、17个月后其中2例复发时又再次升高。晚期卵巢癌患者(Ⅲ - Ⅳ期)的VEGF水平显著高于早期(Ⅰ - Ⅱ期)(P < 0.05)。
血清VEGF水平可作为子宫内膜癌和卵巢癌的一种新的肿瘤标志物,用于疾病的诊断和病情监测。