Alvarez A A, Krigman H R, Whitaker R S, Dodge R K, Rodriguez G C
Department of Obstetrics and Gynecology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Clin Cancer Res. 1999 Mar;5(3):587-91.
The molecular biology underlying the metastatic process in ovarian carcinoma remains poorly understood. For other neoplasms, the induction of angiogenesis by malignant cells has been shown to play a pivotal role in the process of tumor proliferation and metastasis. The purpose of this study was to characterize the degree of angiogenesis in epithelial ovarian malignancies and to determine whether the degree of neovascularization has prognostic significance for survival. Tissue sections obtained from 88 ovarian cancer patients were examined immunohistochemically for angiogenesis after staining with anti-human endothelial cell antibodies to von Willebrand factor and CD31. Light microscopy was performed, and individual microvessel counts were quantified at high power (x400). A chart review was completed, collating data regarding age, stage, grade, status of disease, and survival. Statistical exploratory methods were used to find potentially useful prognostic cutpoints for marker values of angiogenesis. Of the total 88 patients, tissue microvessel counts from 85 were evaluated via antibodies to von Willebrand factor and 87 for CD31. Overall, median survival was 2.7 years in women with cancers containing high microvessel counts versus 7.9 years in those with low microvessel counts (P = 0.03). A low microvessel count was associated with better 5-year survival in both early stage (I and II) and advanced stage (III and IV) disease. Our data suggest that the degree of neovascularization may have prognostic significance in epithelial ovarian carcinoma, especially for women with early-stage disease. In this group of women, the degree of angiogenesis may allow the selection of women at high risk for recurrence who may benefit from aggressive adjuvant therapy.
卵巢癌转移过程背后的分子生物学机制仍未得到充分理解。对于其他肿瘤,恶性细胞诱导血管生成已被证明在肿瘤增殖和转移过程中起关键作用。本研究的目的是描述上皮性卵巢恶性肿瘤中的血管生成程度,并确定新生血管形成程度对生存是否具有预后意义。从88例卵巢癌患者获取的组织切片,在用抗人内皮细胞抗体对血管性血友病因子和CD31进行染色后,进行免疫组织化学检查以检测血管生成情况。进行光学显微镜检查,并在高倍镜(×400)下对单个微血管计数进行量化。完成了一份图表回顾,整理了有关年龄、分期、分级、疾病状态和生存的数据。使用统计探索性方法来寻找血管生成标记值的潜在有用预后切点。在总共88例患者中,85例患者的组织微血管计数通过血管性血友病因子抗体进行评估,87例通过CD31抗体进行评估。总体而言,微血管计数高的癌症女性患者的中位生存期为2.7年,而微血管计数低的患者为7.9年(P = 0.03)。在早期(I期和II期)和晚期(III期和IV期)疾病中,微血管计数低都与更好的5年生存率相关。我们的数据表明,新生血管形成程度可能在上皮性卵巢癌中具有预后意义,特别是对于早期疾病的女性。在这组女性中,血管生成程度可能有助于筛选出复发风险高且可能从积极辅助治疗中获益的女性。