Katsabeki-Katsafli A, Kerenidi T, Kostikas K, Dalaveris E, Kiropoulos T S, Gogou E, Papaioannou A I, Gourgoulianis K I
Respiratory Medicine Department, University of Thessaly Medical School, University Hospital of Larissa, Larissa 41110, Greece.
Lung Cancer. 2008 May;60(2):271-6. doi: 10.1016/j.lungcan.2007.10.006. Epub 2008 Feb 1.
Vascular endothelial growth factor (VEGF) is known to play crucial role in tumour angiogenesis. It is demonstrated that VEGF can be up-regulated by oxidative stress. The aim of this study was to determine the serum VEGF levels and oxidative stress in patients with primary lung cancer and to investigate their association with clinicopathologic factors. We measured serum VEGF levels and oxidative stress in 63 patients (age 63.02+/-1.12 S.E.M.) with primary lung cancer before any treatment (39 NSCLC and 24 SCLC; 6 patients stage I, 3 stage II, 25 stage III and 29 stage IV) and 25 normal subjects. The serum VEGF levels were measured with enzyme linked immunosorbent assay. Serum oxidative stress levels were detected by a commercially available assay (D-ROMs test, Diacron, Grossetto, Italy). The levels of oxidative stress in patients were higher than those in normal subjects (555.3+/-30.35 UCarr vs. 360.1+/-17.46 UCarr). Additionally, a significant difference was found in serum VEGF levels between lung cancer patients and healthy control subjects (428.1+/-38.42pg/ml vs. 298.8+/-19.89pg/ml, respectively, p=0.040). Interestingly, serum oxidative stress presented a significant correlation with serum VEGF levels in patients with lung cancer (r=0.542, p=0.002). Serum VEGF levels were significantly associated with the clinical staging (N-stage) of the patients (p=0.023), performance status (p=0.004) and age (p=0.004). In conclusion, oxidative stress and VEGF are significantly increased in patients with primary lung cancer. The correlation between them might implicate new aspects of the mechanisms controlling tumour angiogenesis and may present clinical interest in the future. Further studies are warranted to evaluate the role of oxidative stress and VEGF as possible biomarkers for the diagnosis and follow-up of patients with lung cancer.
血管内皮生长因子(VEGF)在肿瘤血管生成中起着关键作用。研究表明,氧化应激可上调VEGF。本研究旨在测定原发性肺癌患者的血清VEGF水平和氧化应激,并探讨它们与临床病理因素的关系。我们测量了63例未经任何治疗的原发性肺癌患者(年龄63.02±1.12标准误)(39例非小细胞肺癌和24例小细胞肺癌;6例I期、3例II期、25例III期和29例IV期)及25名正常受试者的血清VEGF水平和氧化应激。采用酶联免疫吸附测定法测量血清VEGF水平。通过市售检测方法(D-ROMs检测,Diacron公司,意大利格罗塞托)检测血清氧化应激水平。患者的氧化应激水平高于正常受试者(555.3±30.35微摩尔/升对360.1±17.46微摩尔/升)。此外,肺癌患者与健康对照者的血清VEGF水平存在显著差异(分别为428.1±38.42皮克/毫升对298.8±19.89皮克/毫升,p = 0.040)。有趣的是,肺癌患者血清氧化应激与血清VEGF水平呈显著相关性(r = 0.542,p = 0.002)。血清VEGF水平与患者的临床分期(N分期)(p = 0.023)、体能状态(p = 0.004)和年龄(p = 0.004)显著相关。总之,原发性肺癌患者的氧化应激和VEGF显著升高。它们之间的相关性可能暗示了控制肿瘤血管生成机制的新方面,并可能在未来引起临床关注。有必要进一步研究评估氧化应激和VEGF作为肺癌患者诊断和随访潜在生物标志物的作用。