Maher Stephen G, Gillham Charles M, Duggan Shane P, Smyth Paul C, Miller Nicola, Muldoon Cian, O'Byrne Kenneth J, Sheils Orla M, Hollywood Donal, Reynolds John V
Department of Surgery, Trinity Centre for Health Sciences, Trinity College Dublin, Dublin, Ireland.
Ann Surg. 2009 Nov;250(5):729-37. doi: 10.1097/SLA.0b013e3181bce7e1.
This study explored gene expression differences in predicting response to chemoradiotherapy in esophageal cancer.
A major pathological response to neoadjuvant chemoradiation is observed in about 40% of esophageal cancer patients and is associated with favorable outcomes. However, patients with tumors of similar histology, differentiation, and stage can have vastly different responses to the same neoadjuvant therapy. This dichotomy may be due to differences in the molecular genetic environment of the tumor cells.
Diagnostic biopsies were obtained from a training cohort of esophageal cancer patients (13), and extracted RNA was hybridized to genome expression microarrays. The resulting gene expression data was verified by qRT-PCR. In a larger, independent validation cohort (27), we examined differential gene expression by qRT-PCR. The ability of differentially-regulated genes to predict response to therapy was assessed in a multivariate leave-one-out cross-validation model.
Although 411 genes were differentially expressed between normal and tumor tissue, only 103 genes were altered between responder and non-responder tumor; and 67 genes differentially expressed >2-fold. These included genes previously reported in esophageal cancer and a number of novel genes. In the validation cohort, 8 of 12 selected genes were significantly different between the response groups. In the predictive model, 5 of 8 genes could predict response to therapy with 95% accuracy in a subset (74%) of patients.
This study has identified a gene microarray pattern and a set of genes associated with response to neoadjuvant chemoradiation in esophageal cancer. The potential of these genes as biomarkers of response to treatment warrants further investigation.
本研究探讨基因表达差异在预测食管癌放化疗反应中的作用。
约40%的食管癌患者在新辅助放化疗后出现主要病理反应,且与良好预后相关。然而,组织学、分化程度和分期相似的肿瘤患者对相同新辅助治疗的反应可能差异极大。这种二分法可能是由于肿瘤细胞分子遗传环境的差异所致。
从一组食管癌患者(13例)的训练队列中获取诊断性活检样本,提取的RNA与基因组表达微阵列杂交。所得基因表达数据通过qRT-PCR进行验证。在一个更大的独立验证队列(27例)中,我们通过qRT-PCR检测差异基因表达。在多变量留一法交叉验证模型中评估差异调节基因预测治疗反应的能力。
尽管正常组织和肿瘤组织之间有411个基因差异表达,但反应者和无反应者肿瘤之间仅103个基因发生改变;67个基因差异表达超过2倍。这些基因包括先前在食管癌中报道的基因以及一些新基因。在验证队列中,12个选定基因中的8个在反应组之间有显著差异。在预测模型中,8个基因中的5个在一部分(74%)患者中能够以95%的准确率预测治疗反应。
本研究确定了一种基因微阵列模式以及一组与食管癌新辅助放化疗反应相关的基因。这些基因作为治疗反应生物标志物的潜力值得进一步研究。