| Literature DB >> 31286759 |
Yukari Totsuka1, Yingsong Lin2, Yutong He3, Kousuke Ishino1, Haruna Sato1, Mamoru Kato4, Momoko Nagai4, Asmaa Elzawahry4, Yasushi Totoki5, Hiromi Nakamura5, Fumie Hosoda5, Tatsuhiro Shibata5, Tomonari Matsuda6, Yoshitaka Matsushima7, Guohui Song8, Fanshu Meng8, Dongfang Li8, Junfeng Liu3, Youlin Qiao9, Wenqiang Wei9, Manami Inoue10, Shogo Kikuchi2, Hitoshi Nakagama11, Baoen Shan3.
Abstract
Esophageal cancer is prevalent in Cixian, China, but the etiology of this disease remains largely unknown. Therefore, we explored this by conducting a DNA adductome analysis. Both tumorous and nontumorous tissues were collected from patients who underwent surgical procedures at Cixian Cancer Hospital and the Fourth Hospital of Hebei Medical University, which is in a low-incidence area. N2-(3,4,5,6-Tetrahydro-2H-pyran-2-yl)deoxyguanosine (THP-dG) was the major adduct detected in samples from esophageal cancer patients in Cixian. The precursor of THP-dG, N-nitrosopiperidine (NPIP), exhibited a strong mutagenic activity under metabolic activation in the Ames test and a significant dose-dependent increase in mutation frequency during an in vivo mutagenicity test with guanine phosphoribosyltransferase (gpt) delta rats. The NPIP-induced mutation was dominated by A:T to C:G transversions, followed by G:C to A:T and A:T to G:C transitions, in the liver and esophagus of animal samples. A similar mutational pattern was observed in the mutational signature of esophageal cancer patients that demonstrated weak correlation with THP-dG levels. These findings suggested that NPIP exposure is partly involved in the development of esophageal cancer in Cixian residents.Entities:
Year: 2019 PMID: 31286759 DOI: 10.1021/acs.chemrestox.9b00017
Source DB: PubMed Journal: Chem Res Toxicol ISSN: 0893-228X Impact factor: 3.739