Korampalli Tirupati S, Stafford Nicholas D
Postgraduate Medical Institute, University of Hull, Castle Hill Hospital, Cottingham, Hull HU16 5JQ, UK.
Mol Clin Oncol. 2013 Nov;1(6):1013-1018. doi: 10.3892/mco.2013.179. Epub 2013 Sep 12.
Over 2,200 cases of carcinoma of the larynx are diagnosed in the UK annually, with an overall 5-year survival rate of 67%. Angiogenesis is vital for the growth and metastasis of solid tumours and the expression of key angiogenesis-related proteins has been shown to be of prognostic significance. In this study we reported the expression of key angiogenesis-related factors, selected from a pilot array study, in a cohort of laryngeal tumours and associated metastatic lymph nodes. Forty patients diagnosed with squamous cell carcinoma of the larynx were recruited. Tissue specimens were obtained intra-operatively, prior to chemo- and/or radiotherapy, from the tumours and secondary lymph nodes. The patient group comprised 32 men and 8 women with a mean age of 68 years (range, 51-89 years). The relative expression of the angiogenesis-related proteins angiogenin, interleukin (IL)-8, tissue inhibitor of metalloproteinases-1 (TIMP-1), vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF)-basic and insulin-like growth factor binding protein 3 (IGFBP3) was determined in the tissue lysates by ELISA. The expression of angiogenin was higher in early-stage compared with late-stage tumours (P=0.034) and the expression of IGFBP3 was higher in tumours compared with the metastatic lymph nodes (P=0.016). No statistically significant differences were recorded for VEGF, FGF, TIMP-1 or IL-8 between tumour stages or primary tumours and lymph nodes. To the best of our knowledge, this study was the first to investigate multiple angiogenic factors in the lysates of laryngeal carcinomas and metastatic nodes and identified angiogenin and IGFBP3 as factors possibly involved in tumour progression. A greater understanding of their function may offer novel prognostic and/or therapeutic options.
英国每年诊断出超过2200例喉癌病例,总体5年生存率为67%。血管生成对于实体肿瘤的生长和转移至关重要,关键血管生成相关蛋白的表达已被证明具有预后意义。在本研究中,我们报告了从一项初步阵列研究中选出的关键血管生成相关因子在一组喉肿瘤及相关转移性淋巴结中的表达情况。招募了40例被诊断为喉鳞状细胞癌的患者。在化疗和/或放疗前,于手术中从肿瘤和继发淋巴结获取组织标本。患者组包括32名男性和8名女性,平均年龄68岁(范围51 - 89岁)。通过酶联免疫吸附测定法(ELISA)测定组织裂解物中血管生成素、白细胞介素(IL)-8、金属蛋白酶组织抑制剂-1(TIMP-1)、血管内皮生长因子(VEGF)、碱性成纤维细胞生长因子(FGF)和胰岛素样生长因子结合蛋白3(IGFBP3)等血管生成相关蛋白的相对表达。血管生成素在早期肿瘤中的表达高于晚期肿瘤(P = 0.034),IGFBP3在肿瘤中的表达高于转移性淋巴结(P = 0.016)。在肿瘤分期之间或原发肿瘤与淋巴结之间,VEGF、FGF、TIMP-1或IL-8未记录到统计学上的显著差异。据我们所知,本研究首次在喉癌和转移性淋巴结的裂解物中研究多种血管生成因子,并确定血管生成素和IGFBP3为可能参与肿瘤进展的因子。对它们功能的更深入了解可能会提供新的预后和/或治疗选择。