• 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

相似文献

1
An Immunohistochemical Study of Anaplastic Lymphoma Kinase and Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Carcinoma.非小细胞肺癌中间变性淋巴瘤激酶和表皮生长因子受体突变的免疫组织化学研究
J Clin Diagn Res. 2017 Jul;11(7):EC22-EC25. doi: 10.7860/JCDR/2017/27941.10279. Epub 2017 Jul 1.
2
Concurrent EGFR Mutation and ALK Translocation in Non-Small Cell Lung Cancer.非小细胞肺癌中的表皮生长因子受体(EGFR)突变与间变性淋巴瘤激酶(ALK)易位并存
Cureus. 2016 Feb 26;8(2):e513. doi: 10.7759/cureus.513.
3
[Advances in Double Mutations of EGFR and ALK Gene in Non-small Cell Lung Cancer].[非小细胞肺癌中表皮生长因子受体(EGFR)和间变性淋巴瘤激酶(ALK)基因双突变的研究进展]
Zhongguo Fei Ai Za Zhi. 2018 Sep 20;21(9):686-691. doi: 10.3779/j.issn.1009-3419.2018.09.07.
4
Case report: Concomitant mutation and rearrangement in non-small cell lung cancer.病例报告:非小细胞肺癌中的伴随突变和重排
Front Pharmacol. 2023 Aug 29;14:1167959. doi: 10.3389/fphar.2023.1167959. eCollection 2023.
5
Differential sensitivities to tyrosine kinase inhibitors in NSCLC harboring EGFR mutation and ALK translocation.非小细胞肺癌中 EGFR 突变和 ALK 易位对酪氨酸激酶抑制剂的敏感性差异。
Lung Cancer. 2012 Aug;77(2):460-3. doi: 10.1016/j.lungcan.2012.04.012. Epub 2012 May 21.
6
Concomitant ALK translocation and EGFR mutation in lung cancer: a comparison of direct sequencing and sensitive assays and the impact on responsiveness to tyrosine kinase inhibitor.肺癌中 ALK 易位与 EGFR 突变的共存:直接测序与敏感检测方法的比较,以及对酪氨酸激酶抑制剂反应性的影响。
Ann Oncol. 2015 Feb;26(2):348-54. doi: 10.1093/annonc/mdu530. Epub 2014 Nov 17.
7
Epidermal Growth Factor Receptor (EGFR) Mutations and Anaplastic Lymphoma Kinase/Oncogene or C-Ros Oncogene 1 (ALK/ROS1) Fusions Inflict Non-Small Cell Lung Cancer (NSCLC) Female Patients Older Than 60 Years of Age.表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶/致癌基因或 C-ROS 癌基因 1(ALK/ROS1)融合使 60 岁以上非小细胞肺癌(NSCLC)女性患者受害。
Med Sci Monit. 2018 Dec 23;24:9364-9369. doi: 10.12659/MSM.911333.
8
Non-small Cell Lung Cancer with Concomitant EGFR, KRAS, and ALK Mutation: Clinicopathologic Features of 12 Cases.伴有EGFR、KRAS和ALK突变的非小细胞肺癌:12例临床病理特征
J Pathol Transl Med. 2016 May;50(3):197-203. doi: 10.4132/jptm.2016.03.09. Epub 2016 Apr 18.
9
Assessment of cytology based molecular analysis to guide targeted therapy in advanced non-small-cell lung cancer.基于细胞学的分子分析在晚期非小细胞肺癌靶向治疗指导中的评估
Oncotarget. 2016 Feb 16;7(7):8332-40. doi: 10.18632/oncotarget.6671.
10
Clinical characteristics associated with ALK rearrangements in never-smokers with pulmonary adenocarcinoma.与从不吸烟的肺腺癌患者中 ALK 重排相关的临床特征。
Lung Cancer. 2014 Feb;83(2):259-64. doi: 10.1016/j.lungcan.2013.11.009. Epub 2013 Nov 20.

引用本文的文献

1
Clinical characteristics and first-line palliative treatment patterns in 3,414 patients with advanced lung cancer in India.印度3414例晚期肺癌患者的临床特征及一线姑息治疗模式
Ecancermedicalscience. 2025 Mar 6;19:1867. doi: 10.3332/ecancer.2025.1867. eCollection 2025.
2
Clinical profile of lung cancer in North India: A 10-year analysis of 1862 patients from a tertiary care center.印度北部肺癌的临床特征:对一家三级医疗中心1862例患者的十年分析。
Lung India. 2020 May-Jun;37(3):190-197. doi: 10.4103/lungindia.lungindia_333_19.

本文引用的文献

1
Clinicopathological and immunohistochemical profile of non-small cell lung carcinoma in a tertiary care medical centre in South India.印度南部一家三级医疗中心非小细胞肺癌的临床病理及免疫组化特征
Lung India. 2014 Jan;31(1):23-8. doi: 10.4103/0970-2113.125889.
2
A prospective, molecular epidemiology study of EGFR mutations in Asian patients with advanced non-small-cell lung cancer of adenocarcinoma histology (PIONEER).一项针对亚洲晚期非小细胞肺癌腺癌组织学患者中表皮生长因子受体突变的前瞻性分子流行病学研究(PIONEER)。
J Thorac Oncol. 2014 Feb;9(2):154-62. doi: 10.1097/JTO.0000000000000033.
3
Testing for ALK rearrangement in lung adenocarcinoma: a multicenter comparison of immunohistochemistry and fluorescent in situ hybridization.检测肺腺癌中的 ALK 重排:免疫组织化学和荧光原位杂交的多中心比较。
Mod Pathol. 2013 Dec;26(12):1545-53. doi: 10.1038/modpathol.2013.87. Epub 2013 Jun 7.
4
Detection of ALK rearrangement by immunohistochemistry in lung adenocarcinoma and the identification of a novel EML4-ALK variant.免疫组织化学检测肺腺癌中的 ALK 重排及新型 EML4-ALK 变异体的鉴定。
J Thorac Oncol. 2013 Jul;8(7):883-91. doi: 10.1097/JTO.0b013e3182904e22.
5
Clinico-pathological profile of lung cancer at AIIMS: a changing paradigm in India.全印医学科学研究所肺癌的临床病理特征:印度的一种转变模式
Asian Pac J Cancer Prev. 2013;14(1):489-94. doi: 10.7314/apjcp.2013.14.1.489.
6
Clinical significance of EML4-ALK fusion gene and association with EGFR and KRAS gene mutations in 208 Chinese patients with non-small cell lung cancer.208 例中国非小细胞肺癌患者中 EML4-ALK 融合基因的临床意义及其与 EGFR 和 KRAS 基因突变的关系。
PLoS One. 2013;8(1):e52093. doi: 10.1371/journal.pone.0052093. Epub 2013 Jan 14.
7
Epidemiology of lung cancer in India: focus on the differences between non-smokers and smokers: a single-centre experience.印度肺癌的流行病学:关注非吸烟者与吸烟者之间的差异:单中心经验
Indian J Cancer. 2012 Jan-Mar;49(1):74-81. doi: 10.4103/0019-509X.98925.
8
Prospective molecular marker analyses of EGFR and KRAS from a randomized, placebo-controlled study of erlotinib maintenance therapy in advanced non-small-cell lung cancer.一项随机、安慰剂对照的厄洛替尼维持治疗晚期非小细胞肺癌的前瞻性分子标志物分析:EGFR 和 KRAS。
J Clin Oncol. 2011 Nov 1;29(31):4113-20. doi: 10.1200/JCO.2010.31.8162. Epub 2011 Oct 3.
9
Personalized medicine in lung cancer: what we need to know.肺癌个体化医学:我们需要了解的内容。
Nat Rev Clin Oncol. 2011 Aug 23;8(11):661-8. doi: 10.1038/nrclinonc.2011.126.
10
Surgical implications of the new IASLC/ATS/ERS adenocarcinoma classification.新 IASLC/ATS/ERS 腺癌分类的手术意义。
Eur Respir J. 2012 Feb;39(2):478-86. doi: 10.1183/09031936.00027511. Epub 2011 Aug 4.

非小细胞肺癌中间变性淋巴瘤激酶和表皮生长因子受体突变的免疫组织化学研究

An Immunohistochemical Study of Anaplastic Lymphoma Kinase and Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Carcinoma.

作者信息

Verma Sonal, Kumar Madhu, Kumari Malti, Mehrotra Raj, Kushwaha R A S, Goel Madhumati, Kumar Ashutosh, Kant Surya

机构信息

Senior Resident, Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India.

Associate Professor, Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India.

出版信息

J Clin Diagn Res. 2017 Jul;11(7):EC22-EC25. doi: 10.7860/JCDR/2017/27941.10279. Epub 2017 Jul 1.

DOI:10.7860/JCDR/2017/27941.10279
PMID:28892905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5583851/
Abstract

INTRODUCTION

Lung cancer is one of the leading causes of cancer related death. Targeted treatment for specific markers may help in reducing the cancer related morbidity and mortality.

AIM

To study expression of Anaplastic Lymphoma Kinase (ALK)and Epidermal Growth Factor Receptor (EGFR) mutations in patients of Non-Small Cell Lung Cancer NSCLC, that are the targets for specific ALK inhibitors and EGFR tyrosine kinase inhibitors.

MATERIALS AND METHODS

Total 69 cases of histologically diagnosed NSCLC were examined retrospectively for immunohistochemical expression of EGFR and ALK, along with positive control of normal placental tissue and anaplastic large cell lymphoma respectively.

RESULTS

Of the NSCLC, Squamous Cell Carcinoma (SCC) accounted for 71.0% and adenocarcinoma was 26.1%. ALK expression was seen in single case of 60-year-old female, non-smoker with adenocarcinoma histology. EGFR expression was seen in both SCC (59.18%) and adenocarcinoma in (77.78%) accounting for 63.77% of all cases. Both ALK and EGFR mutation were mutually exclusive.

CONCLUSION

EGFR expression was seen in 63.77% of cases, highlighting the importance of its use in routine analysis, for targeted therapy and better treatment results. Although, ALK expression was seen in 1.45% of all cases, it is an important biomarker in targeted cancer therapy. Also, the mutually exclusive expression of these two markers need further studies to develop a diagnostic algorithm for NSCLC patients.

摘要

引言

肺癌是癌症相关死亡的主要原因之一。针对特定标志物的靶向治疗可能有助于降低癌症相关的发病率和死亡率。

目的

研究间变性淋巴瘤激酶(ALK)和表皮生长因子受体(EGFR)突变在非小细胞肺癌(NSCLC)患者中的表达情况,这两种标志物分别是特定ALK抑制剂和EGFR酪氨酸激酶抑制剂的作用靶点。

材料与方法

回顾性检查69例经组织学诊断为NSCLC的患者,检测EGFR和ALK的免疫组化表达情况,同时分别以正常胎盘组织和间变性大细胞淋巴瘤作为阳性对照。

结果

在NSCLC中,鳞状细胞癌(SCC)占71.0%,腺癌占26.1%。ALK表达见于1例60岁女性非吸烟腺癌患者。EGFR表达在SCC中占59.18%,在腺癌中占77.78%,占所有病例的63.77%。ALK和EGFR突变相互排斥。

结论

63.77%的病例检测到EGFR表达,凸显了其在常规分析、靶向治疗及改善治疗效果方面的重要性。虽然所有病例中ALK表达仅占1.45%,但它是靶向癌症治疗中的一个重要生物标志物。此外,这两种标志物的相互排斥表达情况需要进一步研究,以开发针对NSCLC患者的诊断算法。