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Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes
The differences in genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma remain unclear. We developed a customized, targeted gene sequencing panel for efficient and sensitive identification of germline variants, including whole-gene deletion types for cancer-related drug-metaboli...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606290/ https://www.ncbi.nlm.nih.gov/pubmed/36289279 http://dx.doi.org/10.1038/s41598-022-22914-6 |
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author | Ohnami, Sumiko Naruoka, Akane Isaka, Mitsuhiro Mizuguchi, Maki Nakatani, Sou Kamada, Fukumi Shimoda, Yuji Sakai, Ai Ohshima, Keiichi Hatakeyama, Keiichi Maruyama, Kouji Ohde, Yasuhisa Kenmotsu, Hirotsugu Takahashi, Toshiaki Akiyama, Yasuto Nagashima, Takeshi Urakami, Kenichi Ohnami, Shumpei Yamaguchi, Ken |
author_facet | Ohnami, Sumiko Naruoka, Akane Isaka, Mitsuhiro Mizuguchi, Maki Nakatani, Sou Kamada, Fukumi Shimoda, Yuji Sakai, Ai Ohshima, Keiichi Hatakeyama, Keiichi Maruyama, Kouji Ohde, Yasuhisa Kenmotsu, Hirotsugu Takahashi, Toshiaki Akiyama, Yasuto Nagashima, Takeshi Urakami, Kenichi Ohnami, Shumpei Yamaguchi, Ken |
author_sort | Ohnami, Sumiko |
collection | PubMed |
description | The differences in genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma remain unclear. We developed a customized, targeted gene sequencing panel for efficient and sensitive identification of germline variants, including whole-gene deletion types for cancer-related drug-metabolizing enzyme genes in lung adenocarcinoma and squamous cell carcinoma. The minor allele frequencies of the variants, confirmed as clinically significant in the Japanese population, did not differ significantly from those of normal participants listed in the public database. Genotype analysis comparing lung adenocarcinoma (n = 559) and squamous cell carcinoma (n = 151) indicated that the variants of DPYD (rs190771411, Fisher’s exact test, P = 0.045; rs200562975, P = 0.045) and ALDH2 (rs568781254, P = 0.032) were associated with an increased risk of squamous cell carcinoma compared to adenocarcinoma. Conversely, whole-gene deletion of CYP2A6 was associated with adenocarcinoma but not squamous cell carcinoma. Notably, whole-gene deletion of CYP2A6 was confirmed in 22 patients with lung adenocarcinoma but not in any patients with squamous cell carcinoma. Most patients with whole-gene deletion of CYP2A6 were female non-smokers. The discovery of a whole-gene deletion of CYP2A6 in patients with lung adenocarcinoma may have an important role in clinical practice and advance our understanding of CYP2A6 germline variants and their association with carcinogenesis or their susceptibility to lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-9606290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96062902022-10-28 Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes Ohnami, Sumiko Naruoka, Akane Isaka, Mitsuhiro Mizuguchi, Maki Nakatani, Sou Kamada, Fukumi Shimoda, Yuji Sakai, Ai Ohshima, Keiichi Hatakeyama, Keiichi Maruyama, Kouji Ohde, Yasuhisa Kenmotsu, Hirotsugu Takahashi, Toshiaki Akiyama, Yasuto Nagashima, Takeshi Urakami, Kenichi Ohnami, Shumpei Yamaguchi, Ken Sci Rep Article The differences in genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma remain unclear. We developed a customized, targeted gene sequencing panel for efficient and sensitive identification of germline variants, including whole-gene deletion types for cancer-related drug-metabolizing enzyme genes in lung adenocarcinoma and squamous cell carcinoma. The minor allele frequencies of the variants, confirmed as clinically significant in the Japanese population, did not differ significantly from those of normal participants listed in the public database. Genotype analysis comparing lung adenocarcinoma (n = 559) and squamous cell carcinoma (n = 151) indicated that the variants of DPYD (rs190771411, Fisher’s exact test, P = 0.045; rs200562975, P = 0.045) and ALDH2 (rs568781254, P = 0.032) were associated with an increased risk of squamous cell carcinoma compared to adenocarcinoma. Conversely, whole-gene deletion of CYP2A6 was associated with adenocarcinoma but not squamous cell carcinoma. Notably, whole-gene deletion of CYP2A6 was confirmed in 22 patients with lung adenocarcinoma but not in any patients with squamous cell carcinoma. Most patients with whole-gene deletion of CYP2A6 were female non-smokers. The discovery of a whole-gene deletion of CYP2A6 in patients with lung adenocarcinoma may have an important role in clinical practice and advance our understanding of CYP2A6 germline variants and their association with carcinogenesis or their susceptibility to lung adenocarcinoma. Nature Publishing Group UK 2022-10-26 /pmc/articles/PMC9606290/ /pubmed/36289279 http://dx.doi.org/10.1038/s41598-022-22914-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ohnami, Sumiko Naruoka, Akane Isaka, Mitsuhiro Mizuguchi, Maki Nakatani, Sou Kamada, Fukumi Shimoda, Yuji Sakai, Ai Ohshima, Keiichi Hatakeyama, Keiichi Maruyama, Kouji Ohde, Yasuhisa Kenmotsu, Hirotsugu Takahashi, Toshiaki Akiyama, Yasuto Nagashima, Takeshi Urakami, Kenichi Ohnami, Shumpei Yamaguchi, Ken Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes |
title | Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes |
title_full | Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes |
title_fullStr | Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes |
title_full_unstemmed | Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes |
title_short | Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes |
title_sort | comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606290/ https://www.ncbi.nlm.nih.gov/pubmed/36289279 http://dx.doi.org/10.1038/s41598-022-22914-6 |
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