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J Mol Diagn. 2010 Jan;12(1):43-50. doi: 10.2353/jmoldx.2010.080131. Epub 2009 Dec 10.
2
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本文引用的文献

1
Cetuximab and chemotherapy as initial treatment for metastatic colorectal cancer.西妥昔单抗与化疗联合作为转移性结直肠癌的初始治疗方案
N Engl J Med. 2009 Apr 2;360(14):1408-17. doi: 10.1056/NEJMoa0805019.
2
Chemotherapy, bevacizumab, and cetuximab in metastatic colorectal cancer.转移性结直肠癌的化疗、贝伐单抗和西妥昔单抗
N Engl J Med. 2009 Feb 5;360(6):563-72. doi: 10.1056/NEJMoa0808268.
3
High-resolution melting analysis for rapid detection of KRAS, BRAF, and PIK3CA gene mutations in colorectal cancer.用于快速检测结直肠癌中KRAS、BRAF和PIK3CA基因突变的高分辨率熔解分析
Am J Clin Pathol. 2008 Aug;130(2):247-53. doi: 10.1309/LWDY1AXHXUULNVHQ.
4
High resolution melting analysis for rapid and sensitive EGFR and KRAS mutation detection in formalin fixed paraffin embedded biopsies.用于福尔马林固定石蜡包埋活检组织中EGFR和KRAS突变快速灵敏检测的高分辨率熔解分析。
BMC Cancer. 2008 May 21;8:142. doi: 10.1186/1471-2407-8-142.
5
Molecular characteristics of bronchioloalveolar carcinoma and adenocarcinoma, bronchioloalveolar carcinoma subtype, predict response to erlotinib.细支气管肺泡癌和腺癌(细支气管肺泡癌亚型)的分子特征可预测对厄洛替尼的反应。
J Clin Oncol. 2008 Mar 20;26(9):1472-8. doi: 10.1200/JCO.2007.13.0062.
6
Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer.野生型KRAS是帕尼单抗对转移性结直肠癌患者疗效所必需的。
J Clin Oncol. 2008 Apr 1;26(10):1626-34. doi: 10.1200/JCO.2007.14.7116. Epub 2008 Mar 3.
7
Prognostic and therapeutic implications of EGFR and KRAS mutations in resected lung adenocarcinoma.表皮生长因子受体(EGFR)和 Kirsten 大鼠肉瘤病毒癌基因同源物(KRAS)突变在切除的肺腺癌中的预后及治疗意义
J Thorac Oncol. 2008 Feb;3(2):111-6. doi: 10.1097/JTO.0b013e318160c607.
8
KRAS mutations as an independent prognostic factor in patients with advanced colorectal cancer treated with cetuximab.KRAS突变作为接受西妥昔单抗治疗的晚期结直肠癌患者的独立预后因素。
J Clin Oncol. 2008 Jan 20;26(3):374-9. doi: 10.1200/JCO.2007.12.5906.
9
Epidermal growth factor receptor mutation detection using high-resolution melting analysis predicts outcomes in patients with advanced non small cell lung cancer treated with gefitinib.使用高分辨率熔解分析检测表皮生长因子受体突变可预测接受吉非替尼治疗的晚期非小细胞肺癌患者的预后。
Clin Cancer Res. 2007 Sep 15;13(18 Pt 1):5385-90. doi: 10.1158/1078-0432.CCR-07-0627.
10
EGFR and K-ras mutation analysis in non-small cell lung cancer: comparison of paraffin embedded versus frozen specimens.非小细胞肺癌中表皮生长因子受体(EGFR)和K-ras基因突变分析:石蜡包埋标本与冰冻标本的比较
Cell Oncol. 2007;29(3):257-64. doi: 10.1155/2007/568205.

KRAS 基因突变:结肠癌检测方法和组织采样技术的比较。

KRAS mutation: comparison of testing methods and tissue sampling techniques in colon cancer.

机构信息

Department of Pathology, University of Colorado Denver, Fitzsimons Campus, 12801 E. 17 Ave., Aurora, CO 80045, USA.

出版信息

J Mol Diagn. 2010 Jan;12(1):43-50. doi: 10.2353/jmoldx.2010.080131. Epub 2009 Dec 10.

DOI:10.2353/jmoldx.2010.080131
PMID:20007845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2797717/
Abstract

Treatment of colon carcinoma with the anti-epidermal growth factor receptor antibody Cetuximab is reported to be ineffective in KRAS-mutant tumors. Mutation testing techniques have therefore become an urgent concern. We have compared three methods for detecting KRAS mutations in 59 cases of colon carcinoma: 1) high resolution melting, 2) the amplification refractory mutation system using a bifunctional self-probing primer (ARMS/Scorpion, ARMS/S), and 3) direct sequencing. We also evaluated the effects of the methods of sectioning and coring of paraffin blocks to obtain tumor DNA on assay sensitivity and specificity. The most sensitive and specific combination of block sampling and mutational analysis was ARMS/S performed on DNA derived from 1-mm paraffin cores. This combination of tissue sampling and testing method detected KRAS mutations in 46% of colon tumors. Four samples were positive by ARMS/S, but initially negative by direct sequencing. Cloned DNA samples were retested by direct sequencing, and in all four cases KRAS mutations were identified in the DNA. In six cases, high resolution melting abnormalities could not be confirmed as specific mutations either by ARMS/S or direct sequencing. We conclude that coring of the paraffin blocks and testing by ARMS/S is a sensitive, specific, and efficient method for KRAS testing.

摘要

用抗表皮生长因子受体抗体西妥昔单抗治疗结肠直肠癌的报道表明,在 KRAS 突变型肿瘤中无效。因此,突变检测技术成为当务之急。我们比较了三种检测 59 例结肠直肠癌中 KRAS 突变的方法:1)高分辨率熔解曲线分析,2)使用双功能自探针引物的扩增受阻突变系统(ARMS/Scorpion,ARMS/S),3)直接测序。我们还评估了获得肿瘤 DNA 的石蜡块切片和芯部取样方法对检测灵敏度和特异性的影响。从 1mm 石蜡芯中获得的 DNA 上进行 ARMS/S 是最敏感和最特异的组合。这种组织取样和检测方法的组合检测到 46%的结肠肿瘤存在 KRAS 突变。4 个样本经 ARMS/S 检测为阳性,但最初经直接测序检测为阴性。对克隆 DNA 样本进行直接测序复测,在所有 4 个病例中均在 DNA 中鉴定出 KRAS 突变。在 6 例中,高分辨率熔解曲线分析的异常不能通过 ARMS/S 或直接测序被确认为特定突变。我们得出结论,石蜡块芯部取样和 ARMS/S 检测是一种敏感、特异和有效的 KRAS 检测方法。