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本文引用的文献

1
Platinum Compound-Related Ototoxicity in Children: Long-Term Follow-Up Reveals Continuous Worsening of Hearing Loss.儿童铂类化合物相关耳毒性:长期随访显示听力损失持续恶化
J Pediatr Hematol Oncol. 2004 Oct;26(10):649-655. doi: 10.1097/01.mph.0000141348.62532.73.
2
The design and screening of drugs to prevent acquired sensorineural hearing loss.用于预防获得性感觉神经性听力损失的药物的设计与筛选。
Expert Opin Drug Discov. 2011 May;6(5):491-505. doi: 10.1517/17460441.2011.562887. Epub 2011 Mar 15.
3
Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey.对38个基因进行筛查后发现,土耳其62%的非综合征性耳聋家庭存在突变。
Genet Test Mol Biomarkers. 2011 Jan-Feb;15(1-2):29-33. doi: 10.1089/gtmb.2010.0120. Epub 2010 Nov 30.
4
Genetic variants associated with cisplatin-induced hearing loss.与顺铂诱导的听力损失相关的基因变异。
Clin Genet. 2010 Jul;78(1):33-5. doi: 10.1111/j.1399-0004.2010.01414_2.x.
5
Organic cation transporter 2 mediates cisplatin-induced oto- and nephrotoxicity and is a target for protective interventions.有机阳离子转运体 2 介导顺铂诱导的耳肾毒性,是保护性干预的靶点。
Am J Pathol. 2010 Mar;176(3):1169-80. doi: 10.2353/ajpath.2010.090610. Epub 2010 Jan 28.
6
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.TPMT 和 COMT 基因变异与接受顺铂化疗的儿童听力损失相关。
Nat Genet. 2009 Dec;41(12):1345-9. doi: 10.1038/ng.478. Epub 2009 Nov 8.
7
Cisplatin ototoxicity and protection: clinical and experimental studies.顺铂耳毒性及其防护:临床与实验研究。
Tohoku J Exp Med. 2009 Nov;219(3):177-86. doi: 10.1620/tjem.219.177.
8
Contribution of organic cation transporter 2 (OCT2) to cisplatin-induced nephrotoxicity.有机阳离子转运体2(OCT2)在顺铂诱导的肾毒性中的作用。
Clin Pharmacol Ther. 2009 Oct;86(4):396-402. doi: 10.1038/clpt.2009.139. Epub 2009 Jul 22.
9
Common variations in ERCC2 are associated with response to cisplatin chemotherapy and clinical outcome in osteosarcoma patients.ERCC2基因的常见变异与骨肉瘤患者对顺铂化疗的反应及临床结局相关。
Pharmacogenomics J. 2009 Oct;9(5):347-53. doi: 10.1038/tpj.2009.19. Epub 2009 May 12.
10
Linkage disequilibrium between two high-frequency deletion polymorphisms: implications for association studies involving the glutathione-S transferase (GST) genes.两个高频缺失多态性之间的连锁不平衡:对涉及谷胱甘肽-S转移酶(GST)基因的关联研究的影响。
PLoS Genet. 2009 May;5(5):e1000472. doi: 10.1371/journal.pgen.1000472. Epub 2009 May 8.

顺铂诱导耳毒性的药物基因组学。

Pharmacogenomics of cisplatin-induced ototoxicity.

机构信息

Department of Surgery, Division of Otolaryngology, Southern Illinois University, School of Medicine, Springfield, IL, USA.

出版信息

Pharmacogenomics. 2011 Jul;12(7):1039-50. doi: 10.2217/pgs.11.48.

DOI:10.2217/pgs.11.48
PMID:21787192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3217465/
Abstract

Cisplatin ototoxicity affects different individuals in a widely variable manner. These variations are likely to be explained by genetic differences among those affected. It would be highly advantageous to identify genetic variants that predispose to cisplatin ototoxicity in order to minimize the risk to susceptible subgroups. Although this area of research is very important, only a few studies have rigorously examined the genetic basis for cisplatin-induced susceptibility to hearing loss. This article addresses recent progress in clarifying the incidence of cisplatin ototoxicity and the risk factors and controversies regarding the identification of genetic variants associated with cisplatin-induced hearing loss.

摘要

顺铂耳毒性对不同个体的影响差异很大。这些差异可能是由受影响个体之间的遗传差异引起的。如果能够识别出导致顺铂耳毒性的遗传变异,将有助于将这种风险最小化易感亚群。尽管这一研究领域非常重要,但只有少数研究严格检查了导致顺铂引起听力损失的遗传基础。本文介绍了阐明顺铂耳毒性的发生率以及与顺铂引起的听力损失相关的遗传变异体的风险因素和争议方面的最新进展。