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Comprehensive analysis of age‐related somatic mutation profiles in Chinese young lung adenocarcinoma patients
BACKGROUND: Lung adenocarcinoma in young adults is a rare entity with the oncogenic genetic alterations associated being poorly understood. In the present study, the effect of genetic alterations in lung adenocarcinoma patients diagnosed in young patients is reported. METHODS: Twenty young lung aden...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488136/ https://www.ncbi.nlm.nih.gov/pubmed/30821106 http://dx.doi.org/10.1002/cam4.1839 |
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author | Yang, Bo Li, Jie Li, Fang Zhou, Hongxia Shi, Weiwei Shi, Huaiyin Sun, Shengjie Sun, Wending Wang, Jinliang Ma, Junxun Yan, Xiang Hu, Yi Jiao, Shunchang |
author_facet | Yang, Bo Li, Jie Li, Fang Zhou, Hongxia Shi, Weiwei Shi, Huaiyin Sun, Shengjie Sun, Wending Wang, Jinliang Ma, Junxun Yan, Xiang Hu, Yi Jiao, Shunchang |
author_sort | Yang, Bo |
collection | PubMed |
description | BACKGROUND: Lung adenocarcinoma in young adults is a rare entity with the oncogenic genetic alterations associated being poorly understood. In the present study, the effect of genetic alterations in lung adenocarcinoma patients diagnosed in young patients is reported. METHODS: Twenty young lung adenocarcinoma patients (age years: median: 33.5, range: 24‐36) were enrolled in the current study and 24 patients who were at common age of the disease onset (age years: median: 61.5, range: 52‐79) were selected for comparison. Paraffin sections of lung adenocarcinoma were analyzed using the whole‐exome sequencing platform. RESULTS: Similar number of somatic mutations per tumor were found in the young patients and their older counterparts. Although no age‐related differences were detected in the numbers of lung adenocarcinoma patients harboring well‐known gene variants, mutations in FRG1 and KMT2C were associated with a younger age especially after correcting for tobacco smoking and sex (FRG1: P = 0.027, KMT2C: P = 0.046). Five genetic variants showed higher alteration frequencies in young patients compared to the unclassified East Asian population, suggesting these mutations as disease‐related hereditary germline variants. CONCLUSIONS: These results suggest different characteristics of lung adenocarcinoma between the young and the patients at common age of onset. Young patients with lung adenocarcinoma have a distinctly unique prevalence of oncogenic genetic alterations. |
format | Online Article Text |
id | pubmed-6488136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64881362019-05-23 Comprehensive analysis of age‐related somatic mutation profiles in Chinese young lung adenocarcinoma patients Yang, Bo Li, Jie Li, Fang Zhou, Hongxia Shi, Weiwei Shi, Huaiyin Sun, Shengjie Sun, Wending Wang, Jinliang Ma, Junxun Yan, Xiang Hu, Yi Jiao, Shunchang Cancer Med Clinical Cancer Research BACKGROUND: Lung adenocarcinoma in young adults is a rare entity with the oncogenic genetic alterations associated being poorly understood. In the present study, the effect of genetic alterations in lung adenocarcinoma patients diagnosed in young patients is reported. METHODS: Twenty young lung adenocarcinoma patients (age years: median: 33.5, range: 24‐36) were enrolled in the current study and 24 patients who were at common age of the disease onset (age years: median: 61.5, range: 52‐79) were selected for comparison. Paraffin sections of lung adenocarcinoma were analyzed using the whole‐exome sequencing platform. RESULTS: Similar number of somatic mutations per tumor were found in the young patients and their older counterparts. Although no age‐related differences were detected in the numbers of lung adenocarcinoma patients harboring well‐known gene variants, mutations in FRG1 and KMT2C were associated with a younger age especially after correcting for tobacco smoking and sex (FRG1: P = 0.027, KMT2C: P = 0.046). Five genetic variants showed higher alteration frequencies in young patients compared to the unclassified East Asian population, suggesting these mutations as disease‐related hereditary germline variants. CONCLUSIONS: These results suggest different characteristics of lung adenocarcinoma between the young and the patients at common age of onset. Young patients with lung adenocarcinoma have a distinctly unique prevalence of oncogenic genetic alterations. John Wiley and Sons Inc. 2019-03-01 /pmc/articles/PMC6488136/ /pubmed/30821106 http://dx.doi.org/10.1002/cam4.1839 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Yang, Bo Li, Jie Li, Fang Zhou, Hongxia Shi, Weiwei Shi, Huaiyin Sun, Shengjie Sun, Wending Wang, Jinliang Ma, Junxun Yan, Xiang Hu, Yi Jiao, Shunchang Comprehensive analysis of age‐related somatic mutation profiles in Chinese young lung adenocarcinoma patients |
title | Comprehensive analysis of age‐related somatic mutation profiles in Chinese young lung adenocarcinoma patients |
title_full | Comprehensive analysis of age‐related somatic mutation profiles in Chinese young lung adenocarcinoma patients |
title_fullStr | Comprehensive analysis of age‐related somatic mutation profiles in Chinese young lung adenocarcinoma patients |
title_full_unstemmed | Comprehensive analysis of age‐related somatic mutation profiles in Chinese young lung adenocarcinoma patients |
title_short | Comprehensive analysis of age‐related somatic mutation profiles in Chinese young lung adenocarcinoma patients |
title_sort | comprehensive analysis of age‐related somatic mutation profiles in chinese young lung adenocarcinoma patients |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488136/ https://www.ncbi.nlm.nih.gov/pubmed/30821106 http://dx.doi.org/10.1002/cam4.1839 |
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