Baruah P, Lee M, Wilson P O G, Odutoye T, Williamson P, Hyde N, Kaski J C, Dumitriu I E
1] Department of ENT, St George's Hospital NHS Trust London, London, UK [2] Department of Oral and Maxillo-Facial Surgery, St George's Hospital NHS Trust London, London, UK [3] Cardiovascular and Cell Sciences Research Institute, St George's University of London, London, UK.
Department of ENT, St George's Hospital NHS Trust London, London, UK.
Br J Cancer. 2015 Aug 11;113(4):653-9. doi: 10.1038/bjc.2015.251. Epub 2015 Jul 14.
Head and neck cancers (HNC) are aggressive tumours. Overexpression of p16 in HNC correlates with human papilloma virus (HPV)-associated HNC that carry a better prognosis than HPV-negative tumours. Angiogenesis is an important factor in tumour progression. Our aim was to dissect the impact of p16 expression on angiogenesis factors in HNC.
Eighteen newly diagnosed HNC patients and controls were analysed. Eleven pro- and anti-angiogenesis factors were quantified using multiplex ELISA in HNC patients and controls. Angiogenesis factors were analysed in tumour tissue using immunohistochemistry.
Circulating levels of endostatin (anti-angiogenesis factor) were higher in the HNC group compared with healthy donors. Interestingly, the pro-angiogenesis factors angiopoietin-1 and vascular endothelial growth factor (VEGF) were significantly higher in patients with p16-negative compared with p16-positive HNC. Moreover, the major source of VEGF in p16-positive HNC tissue was tumour stromal cells. In contrast, both tumour cells and stromal cells expressed VEGF in p16-negative tissue.
We show that p16-negative tumours associate with increased circulating levels of pro-angiogenic VEGF and angiopoietin-1. Tissue expression of VEGF differs between p16-positive and p16-negative tumours. These findings may explain differences in the biological behaviour of p16-positive and p16-negative HNC. Better understanding of mechanisms by which the p16 status influences tumour angiogenesis may guide the development of targeted therapies.
头颈癌(HNC)是侵袭性肿瘤。HNC中p16的过表达与人乳头瘤病毒(HPV)相关的HNC相关,后者的预后优于HPV阴性肿瘤。血管生成是肿瘤进展的一个重要因素。我们的目的是剖析p16表达对HNC中血管生成因子的影响。
分析了18例新诊断的HNC患者和对照。使用多重ELISA对HNC患者和对照中的11种促血管生成和抗血管生成因子进行定量。使用免疫组织化学分析肿瘤组织中的血管生成因子。
与健康供体相比,HNC组中内皮抑素(抗血管生成因子)的循环水平更高。有趣的是,与p16阳性的HNC患者相比,p16阴性患者的促血管生成因子血管生成素-1和血管内皮生长因子(VEGF)明显更高。此外,p16阳性HNC组织中VEGF的主要来源是肿瘤基质细胞。相比之下,肿瘤细胞和基质细胞在p16阴性组织中均表达VEGF。
我们表明,p16阴性肿瘤与促血管生成的VEGF和血管生成素-1的循环水平升高有关。p16阳性和p16阴性肿瘤之间VEGF的组织表达有所不同。这些发现可能解释了p16阳性和p16阴性HNC生物学行为的差异。更好地理解p16状态影响肿瘤血管生成的机制可能会指导靶向治疗的发展。