Young Robin J, Fernando Malee, Hughes David, Brown Nicola J, Woll Penella J
Academic Unit of Clinical Oncology, Weston Park Hospital, Whitham Rd, Sheffield S10 2SJ, UK; Academic Unit of Surgical Oncology, Medical School, Beech Hill Rd, University of Sheffield, Sheffield S10 2RX, UK.
Department of Histopathology, Sheffield Teaching Hospitals NHS Foundation Trust, Glossop Rd, Sheffield S10 2JF, UK.
Exp Mol Pathol. 2014 Aug;97(1):148-53. doi: 10.1016/j.yexmp.2014.06.010. Epub 2014 Jun 28.
Angiosarcomas are rare malignant vascular tumours. Angiosarcoma expression of vascular endothelial growth factor (VEGF) has previously been reported, but angiosarcoma expression of other angiogenic growth factors has not been systematically studied. Non-VEGF angiogenic growth factors are a potential mechanism of resistance to VEGF-targeted therapy, but they also represent potential therapeutic targets. Immunohistochemistry analysis evaluated the expression of 13 angiogenic growth factors and receptors in 27 separate benign and malignant archived human vascular tumour samples. The expression of 55 angiogenesis-related proteins was subsequently profiled in five fresh human angiosarcoma tumour samples using antibody arrays. Angiosarcomas expressed a variety of angiogenic growth factors. Significantly higher levels of Notch1 were detected compared with benign haemangiomas (p=0.033), but lower levels of basic fibroblast growth factor (bFGF) compared to benign haemangiomas (p=0.07) and inflammatory vascular lesions (p=0.009). Vascular tumour expression of FGF receptor (FGFR)-1 correlated with angiopoietin (Ang)-2, Tie2, hepatocyte growth factor (HGF) and Notch1 expression (p=0.001, p=0.001, p<0.001 and p<0.001 respectively). Notch1 also correlated with Tie2 expression (p=0.004). In conclusion, angiosarcomas express multiple angiogenic growth factors. Treatments could be targeted at individual angiogenic growth factors. However, our findings provide a rationale for combination therapy, or for treatments that target common downstream signalling intermediaries, such as Akt, mTOR or ERK.
血管肉瘤是罕见的恶性血管肿瘤。此前已有血管肉瘤表达血管内皮生长因子(VEGF)的报道,但其他血管生成生长因子在血管肉瘤中的表达尚未得到系统研究。非VEGF血管生成生长因子是对VEGF靶向治疗产生耐药性的潜在机制,但它们也代表了潜在的治疗靶点。免疫组织化学分析评估了27份存档的人类良性和恶性血管肿瘤样本中13种血管生成生长因子及其受体的表达。随后,使用抗体阵列对5份新鲜的人类血管肉瘤肿瘤样本中的55种血管生成相关蛋白的表达进行了分析。血管肉瘤表达多种血管生成生长因子。与良性血管瘤相比,Notch1的表达水平显著更高(p = 0.033),但与良性血管瘤(p = 0.07)和炎症性血管病变(p = 0.009)相比,碱性成纤维细胞生长因子(bFGF)的水平更低。血管肿瘤中FGF受体(FGFR)-1的表达与血管生成素(Ang)-2、Tie2、肝细胞生长因子(HGF)和Notch1的表达相关(分别为p = 0.001、p = 0.001、p < 0.001和p < 0.001)。Notch1也与Tie2的表达相关(p = 0.004)。总之,血管肉瘤表达多种血管生成生长因子。治疗可以针对单个血管生成生长因子。然而,我们的研究结果为联合治疗或针对常见下游信号中间体(如Akt、mTOR或ERK)的治疗提供了理论依据。