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鉴定与放射治疗不良反应易感性相关的单核苷酸多态性。

Identification of SNPs associated with susceptibility for development of adverse reactions to radiotherapy.

机构信息

Department of Radiation Oncology, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Pharmacogenomics. 2011 Feb;12(2):267-75. doi: 10.2217/pgs.10.186.

DOI:10.2217/pgs.10.186
PMID:21332318
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3128821/
Abstract

Although cancer treatment with radiation can produce high cure rates, adverse effects often result from radiotherapy. These toxicities are manifested as damage to normal tissues and organs in the radiation field. In recognition of the substantial variation in the intrinsic response of individuals to radiation, an effort began approximately 10 years ago to discover the genetic markers, primarily SNPs, which are associated with susceptibility for the development of these adverse responses to radiation therapy. The goal of this research is to identify the SNPs that could serve as the basis of an assay to predict which cancer patients are most likely to develop complications resulting from radiotherapy. This would permit personalization and optimization of the treatment plan for each cancer patient.

摘要

虽然癌症的放射治疗可以产生很高的治愈率,但放射治疗也常常会产生不良反应。这些毒性表现为放射野内正常组织和器官的损伤。鉴于个体对辐射的内在反应存在很大差异,大约 10 年前,人们开始努力寻找与这些放射治疗不良反应易感性相关的遗传标记物,主要是单核苷酸多态性(SNP)。这项研究的目的是确定可以作为检测基础的 SNP,以预测哪些癌症患者最有可能因放射治疗而产生并发症。这将允许为每个癌症患者制定个性化和优化的治疗计划。

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本文引用的文献

1
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.全基因组关联研究鉴定与接受前列腺癌放射治疗后的非裔美国男性勃起功能障碍发展相关的单核苷酸多态性(SNPs)。
Int J Radiat Oncol Biol Phys. 2010 Dec 1;78(5):1292-300. doi: 10.1016/j.ijrobp.2010.07.036.
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Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines.辐射药效基因组学:一种全基因组关联方法,用于使用人淋巴母细胞系鉴定辐射反应生物标志物。
Genome Res. 2010 Nov;20(11):1482-92. doi: 10.1101/gr.107672.110. Epub 2010 Oct 5.
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Single nucleotide polymorphisms of DNA repair genes as predictors of radioresponse.DNA 修复基因的单核苷酸多态性作为放射反应的预测因子。
Semin Radiat Oncol. 2010 Oct;20(4):232-40. doi: 10.1016/j.semradonc.2010.05.003.
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Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.炎症相关基因中的遗传变异与非小细胞肺癌治疗后辐射诱导的毒性有关。
PLoS One. 2010 Aug 25;5(8):e12402. doi: 10.1371/journal.pone.0012402.
5
Association between genetic polymorphisms in the XRCC1, XRCC3, XPD, GSTM1, GSTT1, MSH2, MLH1, MSH3, and MGMT genes and radiosensitivity in breast cancer patients.X 射线修复交叉互补基因 1(XRCC1)、X 射线修复交叉互补基因 3(XRCC3)、解旋酶基因(XPD)、谷胱甘肽 S-转移酶基因(GSTM1)、谷胱甘肽 S-转移酶基因(GSTT1)、错配修复基因 2(MSH2)、错配修复基因 1(MLH1)、错配修复基因 3(MSH3)和 O6-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)基因多态性与乳腺癌患者放射敏感性的关系。
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Genetic variation in glutathione metabolism and DNA repair genes predicts survival of small-cell lung cancer patients.谷胱甘肽代谢和 DNA 修复基因的遗传变异可预测小细胞肺癌患者的生存。
Ann Oncol. 2010 Oct;21(10):2011-2016. doi: 10.1093/annonc/mdq212. Epub 2010 May 3.
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Oral Oncol. 2010 May;46(5):369-72. doi: 10.1016/j.oraloncology.2010.02.012. Epub 2010 Mar 21.