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Platelet-derived endothelial cell growth factor expression correlates with tumour angiogenesis and prognosis in non-small-cell lung cancer.

机译:非小细胞肺癌中血小板衍生的内皮细胞生长因子表达与肿瘤血管生成和预后相关。

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摘要

Angiogenesis is a recently described prognostic factor in non-small-cell lung cancer. Platelet-derived endothelial cell growth factor (PD-ECGF), shown to be the enzyme thymidine phosphorylase (TP), induces angiogenesis in vitro and in vivo. High intracellular levels of the enzyme are associated with increased chemosensitivity to pyrimidine antimetabolites. PD-ECGF/TP expression was evaluated immunohistochemically in surgically resected specimens from 107 patients with operable non-small-cell lung cancer using the P-GF,44C monoclonal antibody. High expression of PD-ECGF/TP was found in 25% of cases and was associated with high vascular grade (P = 0.01). Fourteen of 32 (44%) high vascular grade tumours showed a positive reactivity for PD-ECGF/TP vs 13/75 (17%) of low/medium vascular grade. Positive expression was observed more frequently in T2-staged cases than in T1 (P = 0.04). While overall survival was not affected (P = 0.09), subset analysis revealed that node-negative patients with positive PD-ECGF/TP expression had a worse prognosis (P = 0.04). The results suggest that PD-ECGF/TP may be an important molecule involved in angiogenesis in non-small-cell lung cancer. Up-regulation of the enzyme defines a more aggressive tumour phenotype in patients with node-negative disease. Assessment of vascular grade and PD-ECGF/TP expression should be taken into account in the design of randomized trials assessing the role of adjuvant chemotherapy in non-small-cell lung cancer.
机译:血管生成是非小细胞肺癌中最近描述的预后因素。血小板衍生的内皮细胞生长因子(PD-ECGF)被证明是胸苷磷酸化酶(TP),可在体内和体外诱导血管生成。酶的高细胞内水平与对嘧啶抗代谢物的化学敏感性增加有关。使用P-GF,44C单克隆抗体对107例可手术的非小细胞肺癌患者的手术切除标本中的PD-ECGF / TP表达进行了免疫组织化学评估。在25%的病例中发现了PD-ECGF / TP的高表达,并且与高血管分级有关(P = 0.01)。 32个高血管级别肿瘤中有14个(PD)对PD-ECGF / TP呈阳性反应,而低/中血管级别肿瘤为13/75(17%)。在T2分期的病例中,与T1期相比,阳性表达更为频繁(P = 0.04)。虽然总生存期未受影响(P = 0.09),但亚组分析显示,PD-ECGF / TP表达阳性的淋巴结阴性患者预后较差(P = 0.04)。结果提示,PD-ECGF / TP可能是非小细胞肺癌血管生成的重要分子。在淋巴结阴性疾病患者中,该酶的上调定义了更具侵略性的肿瘤表型。在评估辅助化疗在非小细胞肺癌中的作用的随机试验设计中,应考虑评估血管等级和PD-ECGF / TP表达。

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