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Non-small cell lung cancer with EML4-ALK translocation in Chinese male never-smokers is characterized with early-onset
BACKGROUND: The translocations of the anaplastic lymphoma kinase (ALK) gene with the echinoderm microtubule-associated protein-like 4 (EML4) gene on chromosome 2p have been identified in non-small-cell lung cancers (NSCLCs) as oncogenic driver mutations. It has been suggested that EML4-ALK fusion is...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240865/ https://www.ncbi.nlm.nih.gov/pubmed/25407901 http://dx.doi.org/10.1186/1471-2407-14-834 |
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author | Guo, Yongjun Ma, Jie Lyu, Xiaodong Liu, Hai Wei, Bing Zhao, Jiuzhou Fu, Shuang Ding, Lu Zhang, Jihong |
author_facet | Guo, Yongjun Ma, Jie Lyu, Xiaodong Liu, Hai Wei, Bing Zhao, Jiuzhou Fu, Shuang Ding, Lu Zhang, Jihong |
author_sort | Guo, Yongjun |
collection | PubMed |
description | BACKGROUND: The translocations of the anaplastic lymphoma kinase (ALK) gene with the echinoderm microtubule-associated protein-like 4 (EML4) gene on chromosome 2p have been identified in non-small-cell lung cancers (NSCLCs) as oncogenic driver mutations. It has been suggested that EML4-ALK fusion is associated with the resistance in NSCLCs to epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs), such as gefitinib and erlotinib. In contrast, ALK tyrosine kinase inhibitor (ALK TKI) crizotinib has shown superior effects in combating NSCLCs with EML4-ALK. Thus, characterization of EML4-ALK fusion genes and clinical features of resulting carcinomas would be a great benefit to disease diagnosis and designing customized treatment plans. Studies have suggested that EML4-ALK translocation occurs more frequently in never-smokers with NSCLC, especially in female patients. However, it is not clear whether this is the case in male patients, too. In this study, we have determined the frequency of EML4-ALK translocation in male never-smokers with NSCLC in a cohort of Chinese patients. The clinical features associated with EML4-ALK translocation were also investigated. METHODS: A cohort of 95 Chinese male never-smokers with NSCLC was enrolled in this study. EML4-ALK fusion genes were detected using one-step real time RT-PCR and DNA sequencing. We further determined the expression levels of ALK mRNA by RT-PCR and ALK protein by immunohistochemistry in these specimens. The clinical features of EML4-ALK–positive carcinomas were also determined. RESULTS: We have identified EML4-ALK fusion genes in 8 out of 95 carcinoma cases, accounting for 8.42% in Chinese male never-smokers with NSCLC. It is significantly higher than that in all Chinese male patients (3.44%) regardless smoking habit. It is also significantly higher than that in all Chinese smokers (8/356 or 2.25%) or in smokers worldwide (2.9%) by comparing to published data. Interestingly, EML4-ALK fusion genes are more frequently found in younger patients and associated with less-differentiated carcinomas. CONCLUSIONS: The frequency of EML4-ALK translocation is strongly associated with smoking habits in Chinese male patients with higher frequency in male never-smokers. EML4-ALK translocation is associated with early-onset and less-differentiated carcinomas. |
format | Online Article Text |
id | pubmed-4240865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42408652014-11-23 Non-small cell lung cancer with EML4-ALK translocation in Chinese male never-smokers is characterized with early-onset Guo, Yongjun Ma, Jie Lyu, Xiaodong Liu, Hai Wei, Bing Zhao, Jiuzhou Fu, Shuang Ding, Lu Zhang, Jihong BMC Cancer Research Article BACKGROUND: The translocations of the anaplastic lymphoma kinase (ALK) gene with the echinoderm microtubule-associated protein-like 4 (EML4) gene on chromosome 2p have been identified in non-small-cell lung cancers (NSCLCs) as oncogenic driver mutations. It has been suggested that EML4-ALK fusion is associated with the resistance in NSCLCs to epidermal growth factor receptor tyrosine kinase inhibitors (EGFR TKIs), such as gefitinib and erlotinib. In contrast, ALK tyrosine kinase inhibitor (ALK TKI) crizotinib has shown superior effects in combating NSCLCs with EML4-ALK. Thus, characterization of EML4-ALK fusion genes and clinical features of resulting carcinomas would be a great benefit to disease diagnosis and designing customized treatment plans. Studies have suggested that EML4-ALK translocation occurs more frequently in never-smokers with NSCLC, especially in female patients. However, it is not clear whether this is the case in male patients, too. In this study, we have determined the frequency of EML4-ALK translocation in male never-smokers with NSCLC in a cohort of Chinese patients. The clinical features associated with EML4-ALK translocation were also investigated. METHODS: A cohort of 95 Chinese male never-smokers with NSCLC was enrolled in this study. EML4-ALK fusion genes were detected using one-step real time RT-PCR and DNA sequencing. We further determined the expression levels of ALK mRNA by RT-PCR and ALK protein by immunohistochemistry in these specimens. The clinical features of EML4-ALK–positive carcinomas were also determined. RESULTS: We have identified EML4-ALK fusion genes in 8 out of 95 carcinoma cases, accounting for 8.42% in Chinese male never-smokers with NSCLC. It is significantly higher than that in all Chinese male patients (3.44%) regardless smoking habit. It is also significantly higher than that in all Chinese smokers (8/356 or 2.25%) or in smokers worldwide (2.9%) by comparing to published data. Interestingly, EML4-ALK fusion genes are more frequently found in younger patients and associated with less-differentiated carcinomas. CONCLUSIONS: The frequency of EML4-ALK translocation is strongly associated with smoking habits in Chinese male patients with higher frequency in male never-smokers. EML4-ALK translocation is associated with early-onset and less-differentiated carcinomas. BioMed Central 2014-11-18 /pmc/articles/PMC4240865/ /pubmed/25407901 http://dx.doi.org/10.1186/1471-2407-14-834 Text en © Guo et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Guo, Yongjun Ma, Jie Lyu, Xiaodong Liu, Hai Wei, Bing Zhao, Jiuzhou Fu, Shuang Ding, Lu Zhang, Jihong Non-small cell lung cancer with EML4-ALK translocation in Chinese male never-smokers is characterized with early-onset |
title | Non-small cell lung cancer with EML4-ALK translocation in Chinese male never-smokers is characterized with early-onset |
title_full | Non-small cell lung cancer with EML4-ALK translocation in Chinese male never-smokers is characterized with early-onset |
title_fullStr | Non-small cell lung cancer with EML4-ALK translocation in Chinese male never-smokers is characterized with early-onset |
title_full_unstemmed | Non-small cell lung cancer with EML4-ALK translocation in Chinese male never-smokers is characterized with early-onset |
title_short | Non-small cell lung cancer with EML4-ALK translocation in Chinese male never-smokers is characterized with early-onset |
title_sort | non-small cell lung cancer with eml4-alk translocation in chinese male never-smokers is characterized with early-onset |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240865/ https://www.ncbi.nlm.nih.gov/pubmed/25407901 http://dx.doi.org/10.1186/1471-2407-14-834 |
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