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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
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.
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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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