Ek Eugene T H, Ojaimi Joseline, Kitagawa Yasuyuki, Choong Peter F M
Department of Orthopaedics, University of Melbourne, St. Vincent's Hospital, Melbourne, Australia.
Oncol Rep. 2006 Jul;16(1):17-23.
The role of angiogenesis as a prognostic indicator in cancer has been extensively studied in recent times with several studies demonstrating a positive correlation for various malignant tumours. However, the role of angiogenesis in osteosarcoma remains a topic of debate. In this study, we aim to evaluate the significance of intratumoural microvessel density (MVD) and the degree of vascular epithelial growth factor (VEGF) expression as markers of angiogenesis and correlate this with disease outcome. Archival paraffin-embedded pre-treatment biopsy tissue of patients treated at St. Vincent's Hospital, Melbourne, with non-metastatic osteosarcoma at initial diagnosis was reviewed. Tissue was processed for immunofluorescent staining of the microvascular endothelial cells with antibodies directed against CD31 and CD34. The degree of angiogenesis was assessed, as determined by the microvessel density (MVD). Further histological examination was performed to assess the degree of VEGF expression. Histological observations were correlated with various clinicopathological factors and patient outcome in terms of recurrence, metastasis and death. Twenty-five cases were reviewed, 15 were male and 10 were female, and the median age was 26 years (range, 13-85). The mean follow-up was 21.5 months (range, 3-75 months). The median MVD was 43 microvessels/0.26 mm2 (range, 25-54) and 46 microvessels/0.26 mm2 (range, 30-58) for CD31 and CD34, respectively. Despite the moderate to high vascularity, there was no significant difference noted between the MVD and disease outcome factors for both CD31 and CD34. There was a trend towards a higher MVD in patients aged > 40 years compared to those < 40 years (p = 0.110 for CD31 and p = 0.097 for CD34). In terms of VEGF expression, 24 of 25 cases demonstrated either moderate or strong expression; however, no prognostic significance was determined. In this study, we were able to demonstrate that osteosarcoma is a relatively vascular tumour; however, the degree of MVD and VEGF expression does not provide prognostic information. It is likely that angiogenesis plays a key role in the pathogenesis of osteosarcoma and is, therefore, a potential target for novel anti-angiogenic therapies.
近年来,血管生成作为癌症预后指标的作用已得到广泛研究,多项研究表明其与各种恶性肿瘤呈正相关。然而,血管生成在骨肉瘤中的作用仍是一个有争议的话题。在本研究中,我们旨在评估肿瘤内微血管密度(MVD)和血管内皮生长因子(VEGF)表达程度作为血管生成标志物的意义,并将其与疾病预后相关联。回顾了墨尔本圣文森特医院收治的初诊为非转移性骨肉瘤患者的存档石蜡包埋预处理活检组织。用针对CD31和CD34的抗体对组织进行处理,以对微血管内皮细胞进行免疫荧光染色。通过微血管密度(MVD)评估血管生成程度。进行进一步的组织学检查以评估VEGF表达程度。组织学观察结果与各种临床病理因素以及患者在复发、转移和死亡方面的预后相关联。共回顾了25例病例,其中男性患者15例,女性患者10例,中位年龄为26岁(范围13 - 85岁)。平均随访时间为21.5个月(范围3 - 75个月)。CD31和CD34的中位MVD分别为43个微血管/0.26平方毫米(范围25 - 54)和46个微血管/0.26平方毫米(范围30 - 58)。尽管血管化程度为中度至高,但CD31和CD34的MVD与疾病预后因素之间均未发现显著差异。与年龄<40岁的患者相比 > 40岁的患者有MVD更高的趋势(CD31的p = 0.110,CD34的p = 0.097)。在VEGF表达方面,25例病例中有24例表现为中度或强表达;然而,未确定其预后意义。在本研究中,我们能够证明骨肉瘤是一种血管相对丰富的肿瘤;然而,MVD和VEGF表达程度并不能提供预后信息。血管生成可能在骨肉瘤的发病机制中起关键作用,因此是新型抗血管生成疗法的潜在靶点。