Montag Michael, Dyckhoff Gerhard, Lohr Jennifer, Helmke Burkhard M, Herrmann Eva, Plinkert Peter K, Herold-Mende Christel
Department of Otorhinolaryngology, Head and Neck Surgery, University of Heidelberg, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany.
Cancer Sci. 2009 Jul;100(7):1210-8. doi: 10.1111/j.1349-7006.2009.01158.x. Epub 2009 Mar 31.
Head and neck squamous cell carcinoma has still a poor prognosis. Since angiogenesis is crucial for tumor growth, a better understanding of the potential clinical relevance as well as the interactions between the numerous proangiogenic growth factors is essential to develop improved therapeutic strategies in these tumors. Expression levels of eight growth factors known to induce angiogenesis (HGF, bFGF, VEGF-A, VEGF-D, PDGF-AB, PDGF-BB, G-CSF, and GM-CSF) were quantitatively measured by ELISA in homogenates of 41 head and neck squamous cell carcinomas. In addition, microvessel density and protein localization of growth factors were assessed by immunohistochemistry. Statistical analysis was performed to assess interrelationships between growth factors analyzed and to correlate protein levels with patient outcome. In 90% of the tissues at least 4/8 growth factors analyzed were detectable. Highest amounts and most frequent expression were found for HGF, bFGF and VEGF-A while PDGF-AB and PDGF-BB were present in two-thirds and G-CSF and GM-CSF in approximately half of the cases. Although there was no significant relation to microvessel density, we identified significant associations for bFGF with HGF and G-CSF as well as of PDGF-AB with those of VEGF-A and PDGF-BB. For the first time we demonstrate that expression levels of HGF as well as that of bFGF and G-CSF in head and neck squamous tumors are negative prognostic factors for patient survival. Our data indicate a network of interrelated and prognostically relevant growth factors in these tumors that have to be taken into consideration when planning an antiangiogenic and antitumor therapy.
头颈部鳞状细胞癌的预后仍然很差。由于血管生成对肿瘤生长至关重要,因此更好地了解潜在的临床相关性以及众多促血管生成生长因子之间的相互作用,对于制定针对这些肿瘤的改进治疗策略至关重要。通过酶联免疫吸附测定法(ELISA)对41例头颈部鳞状细胞癌匀浆中已知可诱导血管生成的8种生长因子(肝细胞生长因子、碱性成纤维细胞生长因子、血管内皮生长因子-A、血管内皮生长因子-D、血小板衍生生长因子-AB、血小板衍生生长因子-BB、粒细胞集落刺激因子和粒细胞-巨噬细胞集落刺激因子)的表达水平进行了定量测定。此外,通过免疫组织化学评估微血管密度和生长因子的蛋白定位。进行统计分析以评估所分析的生长因子之间的相互关系,并将蛋白水平与患者预后相关联。在90%的组织中,至少可检测到4/8种所分析的生长因子。肝细胞生长因子、碱性成纤维细胞生长因子和血管内皮生长因子-A的含量最高且表达最频繁,而血小板衍生生长因子-AB和血小板衍生生长因子-BB在三分之二的病例中存在,粒细胞集落刺激因子和粒细胞-巨噬细胞集落刺激因子在大约一半的病例中存在。虽然与微血管密度没有显著关系,但我们发现碱性成纤维细胞生长因子与肝细胞生长因子和粒细胞集落刺激因子之间存在显著关联,以及血小板衍生生长因子-AB与血管内皮生长因子-A和血小板衍生生长因子-BB之间存在显著关联。我们首次证明,头颈部鳞状肿瘤中肝细胞生长因子以及碱性成纤维细胞生长因子和粒细胞集落刺激因子的表达水平是患者生存的负性预后因素。我们的数据表明,在这些肿瘤中存在一个相互关联且与预后相关的生长因子网络,在规划抗血管生成和抗肿瘤治疗时必须予以考虑。