• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

表皮生长因子受体的第19和21外显子在头颈部鳞状细胞癌中高度保守。

Exons 19 and 21 of epidermal growth factor receptor are highly conserved in squamous cell cancer of the head and neck.

作者信息

Carlson Matthew, Wuertz Beverly, Lin Jizhen, Taylor Randy, Ondrey Frank

机构信息

Department of Otolaryngology, University of Minnesota, MMC 396, 420 Delaware ST SE, Minneapolis, MN 55455, USA.

出版信息

Int J Otolaryngol. 2009;2009:649615. doi: 10.1155/2009/649615. Epub 2010 Jan 5.

DOI:10.1155/2009/649615
PMID:20130810
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2814135/
Abstract

Objective. Epidermal growth factor receptor (EGFR) tyrosine kinase inhibition (TKI) is a promising treatment in upper aerodigestive malignancies. EGFR inhibitors might be more effective in patients whose tumors harbor specific EGFR mutations. The presence of specific EFGR mutations is predictive of over a 75% response rate to TKI therapies as compared to 10% in wild type cases of non-small cell lung cancer. Our objective was to examine whether these mutations might occur in upper aerodigestive cancers. Design. DNA was extracted from 20 head and neck squamous cell tumors and 4 squamous cell carcinoma cell lines and sequenced the receptor using published primer pairs. We then compared the results against published mutations. Results. No exon 19 or 21 mutations were found in any of the 20 tumors and 0 of 4 cell lines. Based on the tumor data we would predict that no greater than 8% of head and neck tumors (CI 97.5%) would be likely to harbor either of these mutations. Conclusions. Our findings are comparable to results recently published of Korean, Austrian, and Spanish patient populations and we conclude that exon 19 and 21 EGFR mutations are not more common in head and neck cancer than in nonsmall-cell carcinoma.

摘要

目的。表皮生长因子受体(EGFR)酪氨酸激酶抑制(TKI)是上呼吸消化道恶性肿瘤一种有前景的治疗方法。EGFR抑制剂可能对肿瘤存在特定EGFR突变的患者更有效。与非小细胞肺癌野生型病例10%的反应率相比,特定EGFR突变的存在预示着对TKI治疗的反应率超过75%。我们的目的是研究这些突变是否可能在上呼吸消化道癌症中出现。设计。从20例头颈部鳞状细胞瘤和4个鳞状癌细胞系中提取DNA,并使用已发表的引物对测定受体序列。然后我们将结果与已发表的突变进行比较。结果。在20个肿瘤和4个细胞系中均未发现19或21外显子突变。根据肿瘤数据,我们预测头颈部肿瘤中不超过8%(97.5%置信区间)可能存在这两种突变中的任何一种。结论。我们的发现与最近发表的韩国、奥地利和西班牙患者群体的结果相当,我们得出结论,EGFR 19和21外显子突变在头颈部癌中并不比在非小细胞癌中更常见。

相似文献

1
Exons 19 and 21 of epidermal growth factor receptor are highly conserved in squamous cell cancer of the head and neck.表皮生长因子受体的第19和21外显子在头颈部鳞状细胞癌中高度保守。
Int J Otolaryngol. 2009;2009:649615. doi: 10.1155/2009/649615. Epub 2010 Jan 5.
2
Detection of EGFR- and HER2-activating mutations in squamous cell carcinoma involving the head and neck.头颈部鳞状细胞癌中表皮生长因子受体(EGFR)和人表皮生长因子受体2(HER2)激活突变的检测
Mod Pathol. 2006 May;19(5):634-40. doi: 10.1038/modpathol.3800552.
3
Response of some head and neck cancers to epidermal growth factor receptor tyrosine kinase inhibitors may be linked to mutation of ERBB2 rather than EGFR.一些头颈癌对表皮生长因子受体酪氨酸激酶抑制剂的反应可能与ERBB2而非EGFR的突变有关。
Clin Cancer Res. 2005 Nov 15;11(22):8105-8. doi: 10.1158/1078-0432.CCR-05-0926.
4
Epidermal growth factor receptor mutations detected by denaturing high-performance liquid chromatography in nonsmall cell lung cancer: impact on response to therapy with epidermal growth factor receptor-tyrosine kinase inhibitors.非小细胞肺癌中变性高效液相色谱法检测表皮生长因子受体突变:对表皮生长因子受体酪氨酸激酶抑制剂治疗反应的影响。
Cancer. 2010 Sep 15;116(18):4309-17. doi: 10.1002/cncr.25214.
5
Epidermal Growth Factor Receptor Mutation (EGFR) Testing for Prediction of Response to EGFR-Targeting Tyrosine Kinase Inhibitor (TKI) Drugs in Patients with Advanced Non-Small-Cell Lung Cancer: An Evidence-Based Analysis.表皮生长因子受体突变(EGFR)检测对晚期非小细胞肺癌患者使用表皮生长因子受体靶向酪氨酸激酶抑制剂(TKI)药物疗效的预测:一项循证分析
Ont Health Technol Assess Ser. 2010;10(24):1-48. Epub 2010 Dec 1.
6
Novel epidermal growth factor receptor mutation-specific antibodies for non-small cell lung cancer: immunohistochemistry as a possible screening method for epidermal growth factor receptor mutations.新型表皮生长因子受体突变特异性抗体在非小细胞肺癌中的应用:免疫组织化学作为表皮生长因子受体突变的一种可能的筛选方法。
J Thorac Oncol. 2010 Oct;5(10):1551-8. doi: 10.1097/JTO.0b013e3181e9da60.
7
Tyrosine kinase inhibitors for epidermal growth factor receptor gene mutation-positive non-small cell lung cancers: an update for recent advances in therapeutics.用于表皮生长因子受体基因突变阳性非小细胞肺癌的酪氨酸激酶抑制剂:治疗学最新进展
J Oncol Pharm Pract. 2016 Jun;22(3):461-76. doi: 10.1177/1078155215577810. Epub 2015 Apr 8.
8
Therapies directed against epidermal growth factor receptor in aerodigestive carcinomas.针对气消化道癌中表皮生长因子受体的疗法。
JAMA. 2007 Jul 4;298(1):70-82. doi: 10.1001/jama.298.1.70.
9
Positive progress for non-small cell lung cancer with epidermal growth factor receptor exon 20 insertion mutations: A novel targeted therapy option.表皮生长因子受体外显子 20 插入突变的非小细胞肺癌的积极进展:一种新的靶向治疗选择。
J Oncol Pharm Pract. 2021 Dec;27(8):2007-2009. doi: 10.1177/10781552211044980. Epub 2021 Sep 27.
10
Epidermal growth factor receptor (EGFR) and squamous cell carcinoma of the skin: molecular bases for EGFR-targeted therapy.表皮生长因子受体 (EGFR) 与皮肤鳞状细胞癌:EGFR 靶向治疗的分子基础。
Pathol Res Pract. 2011 Jun 15;207(6):337-42. doi: 10.1016/j.prp.2011.03.002. Epub 2011 Apr 29.

引用本文的文献

1
Cost-effectiveness analysis comparing companion diagnostic tests for EGFR, ALK, and ROS1 versus next-generation sequencing (NGS) in advanced adenocarcinoma lung cancer patients.比较 EGFR、ALK 和 ROS1 伴随诊断测试与下一代测序(NGS)在晚期肺腺癌患者中的成本效益分析。
BMC Cancer. 2020 Sep 14;20(1):875. doi: 10.1186/s12885-020-07240-2.
2
Prevalence of EGFR Tyrosine Kinase Domain Mutations in Head and Neck Squamous Cell Carcinoma: Cohort Study and Systematic Review.头颈部鳞状细胞癌中表皮生长因子受体酪氨酸激酶结构域突变的患病率:队列研究与系统评价
In Vivo. 2017 Jan 2;31(1):23-34. doi: 10.21873/invivo.11020.

本文引用的文献

1
Human papillomavirus-associated oropharyngeal squamous cell carcinomas: primary tumor burden and survival in surgical patients.人乳头瘤病毒相关的口咽鳞状细胞癌:手术患者的原发肿瘤负荷与生存情况
Ann Otol Rhinol Laryngol. 2009 May;118(5):368-73. doi: 10.1177/000348940911800509.
2
Absence of activating mutations in the EGFR kinase domain in Spanish head and neck cancer patients.西班牙头颈癌患者中表皮生长因子受体(EGFR)激酶结构域无激活突变。
Tumour Biol. 2007;28(5):273-9. doi: 10.1159/000110425. Epub 2007 Oct 26.
3
EGFR tyrosine kinase inhibitors in lung cancer: an evolving story.肺癌中的表皮生长因子受体酪氨酸激酶抑制剂:一个不断发展的故事。
Annu Rev Med. 2008;59:429-42. doi: 10.1146/annurev.med.59.090506.202405.
4
STAT-mediated EGFR signaling in cancer.癌症中STAT介导的表皮生长因子受体信号传导
J Cell Biochem. 2007 Oct 1;102(2):311-9. doi: 10.1002/jcb.21475.
5
Antiangiogenesis, anti-VEGF(R) and outlook.抗血管生成、抗血管内皮生长因子(VEGF)及展望
Recent Results Cancer Res. 2007;176:189-99. doi: 10.1007/978-3-540-46091-6_16.
6
Phase I/II trial of erlotinib and cisplatin in patients with recurrent or metastatic squamous cell carcinoma of the head and neck: a Princess Margaret Hospital phase II consortium and National Cancer Institute of Canada Clinical Trials Group Study.厄洛替尼和顺铂用于复发性或转移性头颈部鳞状细胞癌患者的I/II期试验:玛格丽特公主医院II期联合研究组及加拿大国家癌症研究所临床试验组研究
J Clin Oncol. 2007 Jun 1;25(16):2178-83. doi: 10.1200/JCO.2006.07.6547.
7
Epidermal growth factor receptor mutants from human lung cancers exhibit enhanced catalytic activity and increased sensitivity to gefitinib.来自人类肺癌的表皮生长因子受体突变体表现出增强的催化活性以及对吉非替尼的敏感性增加。
Cancer Res. 2007 Mar 1;67(5):2325-30. doi: 10.1158/0008-5472.CAN-06-4293.
8
Making progress through molecular attacks on cancer.通过对癌症的分子攻击取得进展。
Cold Spring Harb Symp Quant Biol. 2005;70:479-82. doi: 10.1101/sqb.2005.70.034.
9
Molecular targeted therapy of lung cancer: EGFR mutations and response to EGFR inhibitors.肺癌的分子靶向治疗:表皮生长因子受体(EGFR)突变与对EGFR抑制剂的反应
Cold Spring Harb Symp Quant Biol. 2005;70:419-26. doi: 10.1101/sqb.2005.70.043.
10
Targeted therapies in gynecologic cancers.妇科癌症的靶向治疗
Curr Cancer Drug Targets. 2006 Jun;6(4):333-63. doi: 10.2174/156800906777441799.