首页> 外文期刊>Clinical oncology >Gene expression profiles of epidermal growth factor receptor, vascular endothelial growth factor and hypoxia-inducible factor-1 with special reference to local responsiveness to neoadjuvant chemoradiotherapy and disease recurrence after rectal cancer surgery.
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Gene expression profiles of epidermal growth factor receptor, vascular endothelial growth factor and hypoxia-inducible factor-1 with special reference to local responsiveness to neoadjuvant chemoradiotherapy and disease recurrence after rectal cancer surgery.

机译:表皮生长因子受体,血管内皮生长因子和低氧诱导因子-1的基因表达谱,特别涉及对直肠癌手术后新辅助放化疗和疾病复发的局部反应。

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AIMS: To establish a causal relationship between the gene expression profiles of angiogenetic molecular markers, including epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF) and hypoxia-inducible factor-1 (HIF-1), in rectal cancer and the local responsiveness to neoadjuvant chemoradiotherapy and subsequent disease recurrence. MATERIALS AND METHODS: We examined the pre-treatment tumour biopsies (n=40) obtained from patients with rectal adenocarcinoma (clinical International Union Against Cancer stage ll/III) who were scheduled to receive neoadjuvant 5-fluorouracil-based chemoradiotherapy for EGFR, VEGF and HIF-1 expression by quantitative real-time polymerase chain reaction. RESULTS: Responders (patients with significant tumour regression, i.e. pathological grades 2/3) showed significantly lower VEGF, HIF-1 and EGFR gene expression levels than the non-responders (patients with insignificant tumour regression, i.e. pathological grades 0/1) in the pre-treatment tumour biopsies. The elevated expression level of each gene could predict patients with a low response to chemoradiation. During the median follow-up of all patients (41 months; 95% confidence interval 28-60 months), 6/40 (15%) developed disease recurrence. Although local responsiveness to neoadjuvant chemoradiotherapy was associated with neither local nor systemic disease recurrence, lymph node metastasis and an elevated VEGF gene expression level were independent predictors of systemic disease recurrence. The 3-year disease-free survival rates of the patients with lower VEGF or EGFR expression levels were significantly lower than those of patients with higher VEGF or EGFR expression levels. CONCLUSIONS: Analysing VEGF expression levels in rectal cancer may be of benefit in estimating the effects of neoadjuvant chemoradiotherapy and in predicting systemic recurrence after rectal cancer surgery.
机译:目的:建立直肠癌和直肠癌中血管生成分子标志物的基因表达谱之间的因果关系,包括表皮生长因子受体(EGFR),血管内皮生长因子(VEGF)和低氧诱导因子-1(HIF-1)。对新辅助放化疗和随后疾病复发的局部反应。材料和方法:我们检查了从直肠腺癌患者(临床国际抗癌联盟II / III期)获得的治疗前肿瘤活检样品(n = 40),这些患者计划接受基于新辅助5-氟尿嘧啶的EGFR,VEGF放化疗。通过定量实时聚合酶链反应表达HIF-1。结果:应答者(具有显着肿瘤消退,即病理等级为2/3的患者)的VEGF,HIF-1和EGFR基因表达水平显着低于无应答者(具有肿瘤消退的患者,即病理等级为0/1)。治疗前的肿瘤活检。每个基因的表达水平升高可以预测患者对化学放射反应低。在所有患者的中位随访期(41个月; 95%的置信区间28-60个月)中,有6/40(15%)发生了疾病复发。尽管对新辅助放化疗的局部反应与局部或全身性疾病的复发均无关,但淋巴结转移和VEGF基因表达水平升高是全身性疾病复发的独立预测因子。 VEGF或EGFR表达水平较低的患者3年无病生存率显着低于VEGF或EGFR表达水平较高的患者。结论:分析直肠癌中VEGF的表达水平可能有助于评估新辅助放化疗的疗效以及预测直肠癌手术后的全身复发。

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