Abstract

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.

Details

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
Author
Ohnami, Sumiko 1 ; Naruoka, Akane 2 ; Isaka, Mitsuhiro 3 ; Mizuguchi, Maki 1 ; Nakatani, Sou 1 ; Kamada, Fukumi 1 ; Shimoda, Yuji 1 ; Sakai, Ai 4 ; Ohshima, Keiichi 5 ; Hatakeyama, Keiichi 6 ; Maruyama, Kouji 7 ; Ohde, Yasuhisa 3 ; Kenmotsu, Hirotsugu 8 ; Takahashi, Toshiaki 8 ; Akiyama, Yasuto 9 ; Nagashima, Takeshi 4 ; Urakami, Kenichi 1 ; Ohnami, Shumpei 1 ; Yamaguchi, Ken 10 

 Shizuoka Cancer Center Research Institute, Cancer Diagnostics Research Division, Nagaizumi-Cho, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
 Shizuoka Cancer Center Research Institute, Drug Discovery and Development Division, Nagaizumi, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
 Shizuoka Cancer Center Hospital, Division of Thoracic Surgery, Nagaizumi, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
 Shizuoka Cancer Center Research Institute, Cancer Diagnostics Research Division, Nagaizumi-Cho, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501); SRL, Inc, Tokyo, Japan (GRID:grid.410830.e) 
 Shizuoka Cancer Center Research Institute, Medical Genetics Division, Nagaizumi, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
 Shizuoka Cancer Center Research Institute, Cancer Multiomics Division, Nagaizumi, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
 Shizuoka Cancer Center Research Institute, Experimental Animal Facility, Nagaizumi, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
 Shizuoka Cancer Center Hospital, Division of Thoracic Oncology, Nagaizumi, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
 Shizuoka Cancer Center Research Institute, Immunotherapy Division, Nagaizumi, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
10  Shizuoka Cancer Center, Nagaizumi, Japan (GRID:grid.415797.9) (ISNI:0000 0004 1774 9501) 
Publication year
2022
Publication date
2022
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2728849964
Copyright
© The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.