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一项大规模候选基因研究发现,SOD2 和 IL13 中的 SNP 可作为直肠癌术前放化疗反应的预测标志物。

A large-scale candidate gene approach identifies SNPs in SOD2 and IL13 as predictive markers of response to preoperative chemoradiation in rectal cancer.

机构信息

Department of Biology, Val d'Aurelle Cancer Institute, Montpellier, France.

出版信息

Pharmacogenomics J. 2011 Dec;11(6):437-43. doi: 10.1038/tpj.2010.62. Epub 2010 Jul 20.

Abstract

Neoadjuvant radiochemotherapy followed by total mesorectal excision is now the standard treatment for locally advanced rectal cancer. However, tumor response to chemoradiation varies widely among individuals and cannot be determined before the final pathologic evaluation. The aim of this study was to identify germline genetic markers that could predict sensitivity or resistance to preoperative radiochemotherapy (RT-CT) in rectal cancer. We evaluated the predictive value of 128 single-nucleotide polymorphisms (SNPs) in 71 patients preoperatively treated by RT-CT. The selected SNPs were distributed over 76 genes that are involved in various cellular processes such as DNA repair, apoptosis, proliferation or immune response. The SNPs superoxide dismutase 2 (SOD2) rs4880 (P=0.005) and interleukin-13 (IL13) rs1800925 (P=0.0008) were significantly associated with tumor response to chemoradiation. These results reinforce the idea of using germline polymorphisms for personalized treatment.

摘要

新辅助放化疗后行全直肠系膜切除术是局部进展期直肠癌的标准治疗方法。然而,肿瘤对放化疗的反应在个体之间差异很大,在最终的病理评估之前无法确定。本研究旨在确定预测直肠癌术前放化疗(RT-CT)敏感性或耐药性的种系遗传标志物。我们评估了 71 例接受 RT-CT 术前治疗的患者中 128 个单核苷酸多态性(SNP)的预测价值。选择的 SNP 分布在 76 个基因上,这些基因参与各种细胞过程,如 DNA 修复、细胞凋亡、增殖或免疫反应。超氧化物歧化酶 2(SOD2)rs4880(P=0.005)和白细胞介素 13(IL13)rs1800925(P=0.0008)与肿瘤对放化疗的反应显著相关。这些结果进一步证实了利用种系多态性进行个体化治疗的想法。

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