Luzadder Michael M, Minko Irina G, Vartanian Vladimir L, Davenport Marten, Fedorov Lev M, McCullough Amanda K, Lloyd R Stephen
Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, Oregon.
Transgenic Mouse Models Shared Resource, Oregon Health & Science University, Portland, Oregon.
Mol Cancer Res. 2025 Jan 2;23(1):46-58. doi: 10.1158/1541-7786.MCR-24-0577.
Dietary exposure to aflatoxin B1 (AFB1) is a risk factor for the development of hepatocellular carcinomas. Following metabolic activation, AFB1 reacts with guanines to form covalent DNA adducts, which induce high-frequency G > T transversions. The molecular signature associated with these mutational events aligns with the single-base substitution signature 24 (SBS24) in the Catalog of Somatic Mutations in Cancer database. Deficiencies in either base excision repair due to the absence of Nei-like DNA glycosylase 1 (NEIL1) or nucleotide excision repair due to the absence of xeroderma complementation group A protein (XPA) contribute to hepatocellular carcinomas in murine models. In the current study, ultra-low error duplex sequencing was used to characterize mutational profiles in liver DNAs of NEIL1-deficient, XPA-deficient, and DNA repair-proficient mice following neonatal injection of 1 mg/kg AFB1. Analyses of AFB1-induced mutations showed high cosine similarity to SBS24 regardless of repair proficiency status. The absence of NEIL1 resulted in an approximately 30% increase in the frequency of mutations, with the distribution suggesting preferential NEIL1-dependent repair of AFB1 lesions in open chromatin regions. A trend of increased mutagenesis was also observed in the absence of XPA. Consistent with the role of XPA in transcription-coupled repair, mutational profiles in XPA-deficient mice showed disruption of the transcriptional bias in mutations associated with SBS24. Implications: Our findings define the roles of DNA repair pathways in AFB1-induced mutagenesis and carcinogenesis in murine models, with these findings having implications in human health for those with base excision repair and nucleotide excision repair deficiencies.
饮食中接触黄曲霉毒素B1(AFB1)是肝细胞癌发生的一个风险因素。经过代谢激活后,AFB1与鸟嘌呤反应形成共价DNA加合物,从而诱导高频G>T颠换。与这些突变事件相关的分子特征与癌症体细胞突变目录数据库中的单碱基替换特征24(SBS24)一致。由于缺乏Nei样DNA糖基化酶1(NEIL1)导致碱基切除修复缺陷,或由于缺乏着色性干皮病互补组A蛋白(XPA)导致核苷酸切除修复缺陷,都会在小鼠模型中引发肝细胞癌。在本研究中,采用超低错误双链测序来表征新生小鼠注射1 mg/kg AFB1后,NEIL1缺陷、XPA缺陷和DNA修复功能正常的小鼠肝脏DNA中的突变谱。对AFB1诱导突变的分析表明,无论修复功能状态如何,其与SBS24的余弦相似度都很高。NEIL1的缺失导致突变频率增加约30%,其分布表明NEIL1优先依赖修复开放染色质区域中的AFB1损伤。在缺乏XPA的情况下也观察到诱变增加的趋势。与XPA在转录偶联修复中的作用一致,XPA缺陷小鼠的突变谱显示与SBS24相关的突变中的转录偏向性受到破坏。启示:我们的研究结果确定了DNA修复途径在小鼠模型中AFB1诱导的诱变和致癌作用中的作用,这些发现对碱基切除修复和核苷酸切除修复缺陷的人类健康具有启示意义。