Prokopios P. Argyris , Cameron C. Durfee , Zachary J. Seeman , John R. Kalmar , Rachel I. Vogel , Reuben S. Harris
{"title":"DNA胞嘧啶脱氨酶APOBEC3B和化学致癌物4NQO协同作用,在体内加剧口腔肿瘤的发生","authors":"Prokopios P. Argyris , Cameron C. Durfee , Zachary J. Seeman , John R. Kalmar , Rachel I. Vogel , Reuben S. Harris","doi":"10.1016/j.oooo.2025.04.083","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>The APOBEC3-related mutation signatures dominate the mutational landscape of numerous human malignancies. One of the enzymes responsible, APOBEC3B (A3B), converts DNA cytosines to uracils (C-to-U), which become immortalized as C-to-T/-G base substitutions in TC motifs. Oral and oropharyngeal squamous cell carcinomas (SCCs) show elevated <em>A3B</em> mRNA/protein levels and high proportion of APOBEC3 signature mutations. Recently, we reported a mouse model that expresses tumor-like levels of human A3B. Here, we show how endogenous A3B may combine with the exogenous carcinogen 4NQO to promote oral tumorigenesis in vivo.</div></div><div><h3>Materials and Methods</h3><div>Engineered 8-week-old C57BL/6J mice constitutively expressing active human <em>A3B</em> (<em>N</em> = 23) were treated with 4NQO (50 μg/mL in drinking water) for 16 weeks. Animals were reverted to normal water (8 weeks) and sacrificed at the 32nd week. Wildtype C57BL/6 mice (<em>N</em> = 22) and mice expressing a catalytically inactive <em>A3B</em> variant (A3B<sup>E255A</sup>, <em>N</em> = 20) served as controls. Tongues and esophagi were harvested and analyzed histopathologically. A3B levels were confirmed by immunohistochemistry (α-A3B rabbit mAb, 5210-87-13; 1:350 dil.). Differences between groups were analyzed using Poisson regression models; <em>P</em> < .05 considered significant.</div></div><div><h3>Results</h3><div>Nontreated wildtype and A3B-expressing animals presented no lesions. As anticipated, 4NQO caused intraoral and esophageal lesions ranging from squamous papillomas to papillary, noninvasive, high-grade, epithelial dysplasias, and SCCs. Active A3B expression in mice promoted oral and esophageal tumorigenesis compared to wild-type animals (3 vs 1.5 lesions/animal; <em>P</em> = .019). Furthermore, A3B caused a 2.2-fold increase in the frequency of invasive SCCs, predominantly of the tongue (<em>P</em> = .026). By immunohistochemistry, all lesions in A3B-expressing animals showed uniformly strong, nuclear positivity. Notably, oral tumorigenesis was substantially attenuated in A3B<sup>E255A</sup> mice compared to active A3B animals (<em>P</em> = .007); A3B<sup>E255A</sup> mice featured overall lesional burden similar to the wildtype group (<em>P</em> = .362).</div></div><div><h3>Conclusions</h3><div>When active, the mutagenic enzyme A3B functions synergistically with 4NQO to promote oral neoplasia, thus exacerbating tumor load and carcinogenesis.</div></div>","PeriodicalId":49010,"journal":{"name":"Oral Surgery Oral Medicine Oral Pathology Oral Radiology","volume":"140 3","pages":"Page e94"},"PeriodicalIF":1.9000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The DNA cytosine deaminase APOBEC3B and the chemical carcinogen 4NQO synergize to exacerbate oral tumorigenesis in vivo\",\"authors\":\"Prokopios P. Argyris , Cameron C. Durfee , Zachary J. Seeman , John R. Kalmar , Rachel I. Vogel , Reuben S. Harris\",\"doi\":\"10.1016/j.oooo.2025.04.083\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>The APOBEC3-related mutation signatures dominate the mutational landscape of numerous human malignancies. One of the enzymes responsible, APOBEC3B (A3B), converts DNA cytosines to uracils (C-to-U), which become immortalized as C-to-T/-G base substitutions in TC motifs. Oral and oropharyngeal squamous cell carcinomas (SCCs) show elevated <em>A3B</em> mRNA/protein levels and high proportion of APOBEC3 signature mutations. Recently, we reported a mouse model that expresses tumor-like levels of human A3B. Here, we show how endogenous A3B may combine with the exogenous carcinogen 4NQO to promote oral tumorigenesis in vivo.</div></div><div><h3>Materials and Methods</h3><div>Engineered 8-week-old C57BL/6J mice constitutively expressing active human <em>A3B</em> (<em>N</em> = 23) were treated with 4NQO (50 μg/mL in drinking water) for 16 weeks. Animals were reverted to normal water (8 weeks) and sacrificed at the 32nd week. Wildtype C57BL/6 mice (<em>N</em> = 22) and mice expressing a catalytically inactive <em>A3B</em> variant (A3B<sup>E255A</sup>, <em>N</em> = 20) served as controls. Tongues and esophagi were harvested and analyzed histopathologically. A3B levels were confirmed by immunohistochemistry (α-A3B rabbit mAb, 5210-87-13; 1:350 dil.). Differences between groups were analyzed using Poisson regression models; <em>P</em> < .05 considered significant.</div></div><div><h3>Results</h3><div>Nontreated wildtype and A3B-expressing animals presented no lesions. As anticipated, 4NQO caused intraoral and esophageal lesions ranging from squamous papillomas to papillary, noninvasive, high-grade, epithelial dysplasias, and SCCs. Active A3B expression in mice promoted oral and esophageal tumorigenesis compared to wild-type animals (3 vs 1.5 lesions/animal; <em>P</em> = .019). Furthermore, A3B caused a 2.2-fold increase in the frequency of invasive SCCs, predominantly of the tongue (<em>P</em> = .026). By immunohistochemistry, all lesions in A3B-expressing animals showed uniformly strong, nuclear positivity. Notably, oral tumorigenesis was substantially attenuated in A3B<sup>E255A</sup> mice compared to active A3B animals (<em>P</em> = .007); A3B<sup>E255A</sup> mice featured overall lesional burden similar to the wildtype group (<em>P</em> = .362).</div></div><div><h3>Conclusions</h3><div>When active, the mutagenic enzyme A3B functions synergistically with 4NQO to promote oral neoplasia, thus exacerbating tumor load and carcinogenesis.</div></div>\",\"PeriodicalId\":49010,\"journal\":{\"name\":\"Oral Surgery Oral Medicine Oral Pathology Oral Radiology\",\"volume\":\"140 3\",\"pages\":\"Page e94\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-07-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oral Surgery Oral Medicine Oral Pathology Oral Radiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2212440325009526\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oral Surgery Oral Medicine Oral Pathology Oral Radiology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2212440325009526","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
The DNA cytosine deaminase APOBEC3B and the chemical carcinogen 4NQO synergize to exacerbate oral tumorigenesis in vivo
Introduction
The APOBEC3-related mutation signatures dominate the mutational landscape of numerous human malignancies. One of the enzymes responsible, APOBEC3B (A3B), converts DNA cytosines to uracils (C-to-U), which become immortalized as C-to-T/-G base substitutions in TC motifs. Oral and oropharyngeal squamous cell carcinomas (SCCs) show elevated A3B mRNA/protein levels and high proportion of APOBEC3 signature mutations. Recently, we reported a mouse model that expresses tumor-like levels of human A3B. Here, we show how endogenous A3B may combine with the exogenous carcinogen 4NQO to promote oral tumorigenesis in vivo.
Materials and Methods
Engineered 8-week-old C57BL/6J mice constitutively expressing active human A3B (N = 23) were treated with 4NQO (50 μg/mL in drinking water) for 16 weeks. Animals were reverted to normal water (8 weeks) and sacrificed at the 32nd week. Wildtype C57BL/6 mice (N = 22) and mice expressing a catalytically inactive A3B variant (A3BE255A, N = 20) served as controls. Tongues and esophagi were harvested and analyzed histopathologically. A3B levels were confirmed by immunohistochemistry (α-A3B rabbit mAb, 5210-87-13; 1:350 dil.). Differences between groups were analyzed using Poisson regression models; P < .05 considered significant.
Results
Nontreated wildtype and A3B-expressing animals presented no lesions. As anticipated, 4NQO caused intraoral and esophageal lesions ranging from squamous papillomas to papillary, noninvasive, high-grade, epithelial dysplasias, and SCCs. Active A3B expression in mice promoted oral and esophageal tumorigenesis compared to wild-type animals (3 vs 1.5 lesions/animal; P = .019). Furthermore, A3B caused a 2.2-fold increase in the frequency of invasive SCCs, predominantly of the tongue (P = .026). By immunohistochemistry, all lesions in A3B-expressing animals showed uniformly strong, nuclear positivity. Notably, oral tumorigenesis was substantially attenuated in A3BE255A mice compared to active A3B animals (P = .007); A3BE255A mice featured overall lesional burden similar to the wildtype group (P = .362).
Conclusions
When active, the mutagenic enzyme A3B functions synergistically with 4NQO to promote oral neoplasia, thus exacerbating tumor load and carcinogenesis.
期刊介绍:
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology is required reading for anyone in the fields of oral surgery, oral medicine, oral pathology, oral radiology or advanced general practice dentistry. It is the only major dental journal that provides a practical and complete overview of the medical and surgical techniques of dental practice in four areas. Topics covered include such current issues as dental implants, treatment of HIV-infected patients, and evaluation and treatment of TMJ disorders. The official publication for nine societies, the Journal is recommended for initial purchase in the Brandon Hill study, Selected List of Books and Journals for the Small Medical Library.