Cargando…
Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China
BACKGROUND: The lung cancer mortality rate in Xuanwei city is among the highest in China and adenocarcinoma is the major histological type. Lung cancer has been associated with exposure to indoor smoky coal emissions that contain high levels of polycyclic aromatic hydrocarbons; however, the pathogen...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334298/ https://www.ncbi.nlm.nih.gov/pubmed/28083984 http://dx.doi.org/10.1111/1759-7714.12411 |
_version_ | 1782511825447813120 |
---|---|
author | Wang, Xiao Li, Jing Duan, Yong Wu, Huifei Xu, Qiuyue Zhang, Yanliang |
author_facet | Wang, Xiao Li, Jing Duan, Yong Wu, Huifei Xu, Qiuyue Zhang, Yanliang |
author_sort | Wang, Xiao |
collection | PubMed |
description | BACKGROUND: The lung cancer mortality rate in Xuanwei city is among the highest in China and adenocarcinoma is the major histological type. Lung cancer has been associated with exposure to indoor smoky coal emissions that contain high levels of polycyclic aromatic hydrocarbons; however, the pathogenesis of lung cancer has not yet been fully elucidated. METHODS: We performed whole genome sequencing with lung adenocarcinoma and corresponding non‐tumor tissue to explore the genomic features of Xuanwei lung cancer. We used the Molecule Annotation System to determine and plot alterations in genes and signaling pathways. RESULTS: A total of 3 428 060 and 3 416 989 single nucleotide variants were detected in tumor and normal genomes, respectively. After comparison of these two genomes, 977 high‐confidence somatic single nucleotide variants were identified. We observed a remarkably high proportion of C·G‐A·T transversions. HECTD4, RCBTB2, KLF15, and CACNA1C may be cancer‐related genes. Nine copy number variations increased in chromosome 5 and one in chromosome 7. The novel junctions were detected via clustered discordant paired ends and 1955 structural variants were discovered. Among these, we found 44 novel chromosome structural variations. In addition, EGFR and CACNA1C in the mitogen‐activated protein kinase signaling pathway were mutated or amplified in lung adenocarcinoma tumor tissue. CONCLUSION: We obtained a comprehensive view of somatic alterations of Xuanwei lung adenocarcinoma. These findings provide insight into the genomic landscape in order to further learn about the progress and development of Xuanwei lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-5334298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53342982017-03-06 Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China Wang, Xiao Li, Jing Duan, Yong Wu, Huifei Xu, Qiuyue Zhang, Yanliang Thorac Cancer Original Articles BACKGROUND: The lung cancer mortality rate in Xuanwei city is among the highest in China and adenocarcinoma is the major histological type. Lung cancer has been associated with exposure to indoor smoky coal emissions that contain high levels of polycyclic aromatic hydrocarbons; however, the pathogenesis of lung cancer has not yet been fully elucidated. METHODS: We performed whole genome sequencing with lung adenocarcinoma and corresponding non‐tumor tissue to explore the genomic features of Xuanwei lung cancer. We used the Molecule Annotation System to determine and plot alterations in genes and signaling pathways. RESULTS: A total of 3 428 060 and 3 416 989 single nucleotide variants were detected in tumor and normal genomes, respectively. After comparison of these two genomes, 977 high‐confidence somatic single nucleotide variants were identified. We observed a remarkably high proportion of C·G‐A·T transversions. HECTD4, RCBTB2, KLF15, and CACNA1C may be cancer‐related genes. Nine copy number variations increased in chromosome 5 and one in chromosome 7. The novel junctions were detected via clustered discordant paired ends and 1955 structural variants were discovered. Among these, we found 44 novel chromosome structural variations. In addition, EGFR and CACNA1C in the mitogen‐activated protein kinase signaling pathway were mutated or amplified in lung adenocarcinoma tumor tissue. CONCLUSION: We obtained a comprehensive view of somatic alterations of Xuanwei lung adenocarcinoma. These findings provide insight into the genomic landscape in order to further learn about the progress and development of Xuanwei lung adenocarcinoma. John Wiley & Sons Australia, Ltd 2017-01-13 2017-03 /pmc/articles/PMC5334298/ /pubmed/28083984 http://dx.doi.org/10.1111/1759-7714.12411 Text en © 2017 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Wang, Xiao Li, Jing Duan, Yong Wu, Huifei Xu, Qiuyue Zhang, Yanliang Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China |
title | Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China |
title_full | Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China |
title_fullStr | Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China |
title_full_unstemmed | Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China |
title_short | Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China |
title_sort | whole genome sequencing analysis of lung adenocarcinoma in xuanwei, china |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334298/ https://www.ncbi.nlm.nih.gov/pubmed/28083984 http://dx.doi.org/10.1111/1759-7714.12411 |
work_keys_str_mv | AT wangxiao wholegenomesequencinganalysisoflungadenocarcinomainxuanweichina AT lijing wholegenomesequencinganalysisoflungadenocarcinomainxuanweichina AT duanyong wholegenomesequencinganalysisoflungadenocarcinomainxuanweichina AT wuhuifei wholegenomesequencinganalysisoflungadenocarcinomainxuanweichina AT xuqiuyue wholegenomesequencinganalysisoflungadenocarcinomainxuanweichina AT zhangyanliang wholegenomesequencinganalysisoflungadenocarcinomainxuanweichina |