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Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing
Lung cancer remains the most prevalent malignancy and the primary cause of cancer-related deaths worldwide. Unique mutations patterns can be found in lung cancer subtypes, in individual cancers, or within a single tumor, and drugs that target these genetic mutations and signal transduction pathways...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489668/ https://www.ncbi.nlm.nih.gov/pubmed/26244006 http://dx.doi.org/10.4137/CIN.S22941 |
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author | Feng, Hongxiang Wang, Xiaowei Zhang, Zhenrong Tang, Chuanning Ye, Hua Jones, Lindsey Lou, Feng Zhang, Dandan Jiang, Shouwen Sun, Hong Dong, Haichao Zhang, Guangchun Liu, Zhiyuan Dong, Zhishou Guo, Baishuai Yan, He Yan, Chaowei Wang, Lu Su, Ziyi Li, Yangyang Nandakumar, Vijayalakshmi Huang, Xue F Chen, Si-Yi Liu, Deruo |
author_facet | Feng, Hongxiang Wang, Xiaowei Zhang, Zhenrong Tang, Chuanning Ye, Hua Jones, Lindsey Lou, Feng Zhang, Dandan Jiang, Shouwen Sun, Hong Dong, Haichao Zhang, Guangchun Liu, Zhiyuan Dong, Zhishou Guo, Baishuai Yan, He Yan, Chaowei Wang, Lu Su, Ziyi Li, Yangyang Nandakumar, Vijayalakshmi Huang, Xue F Chen, Si-Yi Liu, Deruo |
author_sort | Feng, Hongxiang |
collection | PubMed |
description | Lung cancer remains the most prevalent malignancy and the primary cause of cancer-related deaths worldwide. Unique mutations patterns can be found in lung cancer subtypes, in individual cancers, or within a single tumor, and drugs that target these genetic mutations and signal transduction pathways are often beneficial to patients. In this study, we used the Ion Torrent AmpliSeq Cancer Panel to sequence 737 loci from 45 cancer-related genes and oncogenes to identify genetic mutations in 48 formalin-fixed, paraffin-embedded (FFPE) human lung cancer samples from Chinese patients. We found frequent mutations in EGFR, KRAS, PIK3CA, and TP53 genes. Moreover, we observed that a portion of the lung cancer samples harbored two or more mutations in these key genes. This study demonstrates the feasibility of using the Ion Torrent sequencing to efficiently identify genetic mutations in individual tumors for targeted lung cancer therapy. |
format | Online Article Text |
id | pubmed-4489668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-44896682015-08-04 Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing Feng, Hongxiang Wang, Xiaowei Zhang, Zhenrong Tang, Chuanning Ye, Hua Jones, Lindsey Lou, Feng Zhang, Dandan Jiang, Shouwen Sun, Hong Dong, Haichao Zhang, Guangchun Liu, Zhiyuan Dong, Zhishou Guo, Baishuai Yan, He Yan, Chaowei Wang, Lu Su, Ziyi Li, Yangyang Nandakumar, Vijayalakshmi Huang, Xue F Chen, Si-Yi Liu, Deruo Cancer Inform Original Research Lung cancer remains the most prevalent malignancy and the primary cause of cancer-related deaths worldwide. Unique mutations patterns can be found in lung cancer subtypes, in individual cancers, or within a single tumor, and drugs that target these genetic mutations and signal transduction pathways are often beneficial to patients. In this study, we used the Ion Torrent AmpliSeq Cancer Panel to sequence 737 loci from 45 cancer-related genes and oncogenes to identify genetic mutations in 48 formalin-fixed, paraffin-embedded (FFPE) human lung cancer samples from Chinese patients. We found frequent mutations in EGFR, KRAS, PIK3CA, and TP53 genes. Moreover, we observed that a portion of the lung cancer samples harbored two or more mutations in these key genes. This study demonstrates the feasibility of using the Ion Torrent sequencing to efficiently identify genetic mutations in individual tumors for targeted lung cancer therapy. Libertas Academica 2015-06-29 /pmc/articles/PMC4489668/ /pubmed/26244006 http://dx.doi.org/10.4137/CIN.S22941 Text en © 2015 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License. |
spellingShingle | Original Research Feng, Hongxiang Wang, Xiaowei Zhang, Zhenrong Tang, Chuanning Ye, Hua Jones, Lindsey Lou, Feng Zhang, Dandan Jiang, Shouwen Sun, Hong Dong, Haichao Zhang, Guangchun Liu, Zhiyuan Dong, Zhishou Guo, Baishuai Yan, He Yan, Chaowei Wang, Lu Su, Ziyi Li, Yangyang Nandakumar, Vijayalakshmi Huang, Xue F Chen, Si-Yi Liu, Deruo Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing |
title | Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing |
title_full | Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing |
title_fullStr | Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing |
title_full_unstemmed | Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing |
title_short | Identification of Genetic Mutations in Human Lung Cancer by Targeted Sequencing |
title_sort | identification of genetic mutations in human lung cancer by targeted sequencing |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489668/ https://www.ncbi.nlm.nih.gov/pubmed/26244006 http://dx.doi.org/10.4137/CIN.S22941 |
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