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Immunohistochemical detections of EGFR mutations in NSCLC
In recent years, it has been well known that non-small cell lung cancer (NSCLC) patients with mutations of epidermal growth factor receptor (EGFR) response better to EGFR-tyrosine kinase inhibitor treatment. Although DNA-based assays (e.g. DNA sequencing) are the most frequently used and a relativel...
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Published in: | Zhongguo fei ai za zhi 2014-09, Vol.17 (9), p.701-705 |
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description | In recent years, it has been well known that non-small cell lung cancer (NSCLC) patients with mutations of epidermal growth factor receptor (EGFR) response better to EGFR-tyrosine kinase inhibitor treatment. Although DNA-based assays (e.g. DNA sequencing) are the most frequently used and a relatively reliable method to detect EGFR mutations, they are complex, time-consuming and relatively expensive for routine use in clinical laboratories, besides they require high quality tumor samples. In contrast, the immunohistochemistry (IHC) methods make up fully for the above shortcomings and can serve as screening tests for EGFR mutations. However, there are many factors that can influence the results of IHC methods, such as different staining procedures, different antigen retrieval solutions and different sets of criteria, etc. Thus the IHC methods for detecting EGFR mutations have not been widely used in clinic and only in the research stage. This article reviews the use of IHC methods by different researchers and f |
doi_str_mv | 10.3779/j.issn.1009-3419.2014.09.11 |
format | article |
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Although DNA-based assays (e.g. DNA sequencing) are the most frequently used and a relatively reliable method to detect EGFR mutations, they are complex, time-consuming and relatively expensive for routine use in clinical laboratories, besides they require high quality tumor samples. In contrast, the immunohistochemistry (IHC) methods make up fully for the above shortcomings and can serve as screening tests for EGFR mutations. However, there are many factors that can influence the results of IHC methods, such as different staining procedures, different antigen retrieval solutions and different sets of criteria, etc. Thus the IHC methods for detecting EGFR mutations have not been widely used in clinic and only in the research stage. This article reviews the use of IHC methods by different researchers and f</description><identifier>ISSN: 1009-3419</identifier><identifier>EISSN: 1999-6187</identifier><identifier>DOI: 10.3779/j.issn.1009-3419.2014.09.11</identifier><identifier>PMID: 25248714</identifier><language>chi</language><publisher>China: Chinese Anti-Cancer Association Chinese Antituberculosis Association</publisher><subject>Cancer therapies ; Carcinoma, Non-Small-Cell Lung - enzymology ; Carcinoma, Non-Small-Cell Lung - genetics ; DNA Mutational Analysis - methods ; Epidermal growth factor ; Epidermal growth factor receptor ; Humans ; Immunoglobulins ; Immunohistochemistry ; Immunohistochemistry - methods ; Lung cancer ; Lung neoplasms ; Lung Neoplasms - enzymology ; Lung Neoplasms - genetics ; Mutation ; Receptor, Epidermal Growth Factor - genetics</subject><ispartof>Zhongguo fei ai za zhi, 2014-09, Vol.17 (9), p.701-705</ispartof><rights>Copyright © 2014. 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subjects | Cancer therapies Carcinoma, Non-Small-Cell Lung - enzymology Carcinoma, Non-Small-Cell Lung - genetics DNA Mutational Analysis - methods Epidermal growth factor Epidermal growth factor receptor Humans Immunoglobulins Immunohistochemistry Immunohistochemistry - methods Lung cancer Lung neoplasms Lung Neoplasms - enzymology Lung Neoplasms - genetics Mutation Receptor, Epidermal Growth Factor - genetics |
title | Immunohistochemical detections of EGFR mutations in NSCLC |
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