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Non-small cell lung cancer.非小细胞肺癌。
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2
A C118T polymorphism of ERCC1 and response to cisplatin chemotherapy in patients with late-stage non-small cell lung cancer.ERCC1 的 C118T 多态性与晚期非小细胞肺癌患者对顺铂化疗的反应。
J Cancer Res Clin Oncol. 2012 Feb;138(2):231-8. doi: 10.1007/s00432-011-1090-1. Epub 2011 Nov 20.
3
Association between polymorphisms of ERCC1 and XPD and clinical response to platinum-based chemotherapy in advanced non-small cell lung cancer.ERCC1 和 XPD 多态性与晚期非小细胞肺癌铂类化疗临床反应的相关性。
Am J Clin Oncol. 2010 Oct;33(5):489-94. doi: 10.1097/COC.0b013e3181b9cedc.
4
Platinum resistance: the role of DNA repair pathways.铂耐药:DNA修复途径的作用。
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Current status of excision repair cross complementing-group 1 (ERCC1) in cancer.癌症中切除修复交叉互补基因1(ERCC1)的现状
Cancer Treat Rev. 2007 Oct;33(6):565-77. doi: 10.1016/j.ctrv.2007.07.001. Epub 2007 Aug 17.
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Cisplatin- versus carboplatin-based chemotherapy in first-line treatment of advanced non-small-cell lung cancer: an individual patient data meta-analysis.顺铂与卡铂为基础的化疗用于晚期非小细胞肺癌一线治疗的个体患者数据荟萃分析
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Genetic polymorphisms and treatment response in advanced non-small cell lung cancer.晚期非小细胞肺癌的基因多态性与治疗反应
Lung Cancer. 2007 May;56(2):281-8. doi: 10.1016/j.lungcan.2006.12.002. Epub 2007 Jan 12.
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Molecular mechanisms of resistance and toxicity associated with platinating agents.与铂类药物相关的耐药性和毒性的分子机制。
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The treatment of advanced non-small cell lung cancer.晚期非小细胞肺癌的治疗
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10
Low ERCC1 expression correlates with prolonged survival after cisplatin plus gemcitabine chemotherapy in non-small cell lung cancer.在非小细胞肺癌中,ERCC1低表达与顺铂联合吉西他滨化疗后生存期延长相关。
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ERCC1(C118T)基因多态性对接受铂类化疗的晚期非小细胞肺癌患者治疗反应的影响。

Effect of the ERCC1 (C118T) Polymorphism on Treatment Response in Advanced Non-Small Cell Lung Cancer Patients Undergoing Platinum-Based Chemotherapy.

作者信息

Kaewbubpa Walennee, Areepium Nutthada, Sriuranpong Virote

机构信息

Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand. Email:

出版信息

Asian Pac J Cancer Prev. 2016 Nov 1;17(11):4917-4920. doi: 10.22034/APJCP.2016.17.11.4917.

DOI:10.22034/APJCP.2016.17.11.4917
PMID:28032496
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5454696/
Abstract

For advanced non-small-cell lung cancer (NSCLC) cases, a platinum-based regimen is the first-line chemotherapy treatment. The excision repair cross-complementing group 1 (ERCC1) plays an important role in DNA repair and has been related to resistance to platinum chemotherapy. This study aimed to investigate the effects of the ERCC1 (C118T) polymorphism on treatment response in 26 Thai advanced NSCLC patients receiving first line platinum-based chemotherapy during January to July 2015 at King Chulalongkorn Memorial Hospital (KCMH). DNA was extracted from peripheral blood lymphocytes and the single nucleotide polymorphism of ERCC1 was genotyped using a realtime PCR method with the TaqMan assay. The distribution of C/C, C/T and T/T genotypes was 57.7 %, 34.6 % and 7.7 %, respectively. The response rate to platinum-based chemotherapy in the wild type (C/C) of ERCC1 (C118T) was better than with the variant types (C/T and T/T) but the difference was not statistically significant (29.7% vs 9.1%, P=0.274). The results showed that a genetic polymorphism in ERCC1 might influence patient response to platinumbased chemotherapy. Further multicenter studies are now required to confirm the results of our study.

摘要

对于晚期非小细胞肺癌(NSCLC)病例,铂类方案是一线化疗治疗方法。切除修复交叉互补组1(ERCC1)在DNA修复中起重要作用,并且与铂类化疗耐药相关。本研究旨在调查2015年1月至7月期间在朱拉隆功国王纪念医院(KCMH)接受一线铂类化疗的26例泰国晚期NSCLC患者中,ERCC1(C118T)基因多态性对治疗反应的影响。从外周血淋巴细胞中提取DNA,并使用TaqMan分析法通过实时PCR方法对ERCC1的单核苷酸多态性进行基因分型。C/C、C/T和T/T基因型的分布分别为57.7%、34.6%和7.7%。ERCC1(C118T)野生型(C/C)对铂类化疗的反应率优于变异型(C/T和T/T),但差异无统计学意义(29.7%对9.1%,P = 0.274)。结果表明,ERCC1基因多态性可能影响患者对铂类化疗的反应。现在需要进一步的多中心研究来证实我们的研究结果。