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过氧化氢诱导的 8-氧鸟嘌呤模式与上消化道肿瘤的两种癌症突变特征的一致性。

Concordance of hydrogen peroxide-induced 8-oxo-guanine patterns with two cancer mutation signatures of upper GI tract tumors.

机构信息

Department of Epigenetics, Van Andel Institute, Grand Rapids, MI 49503, USA.

出版信息

Sci Adv. 2022 Jun 3;8(22):eabn3815. doi: 10.1126/sciadv.abn3815.

Abstract

Oxidative DNA damage has been linked to inflammation, cancer, and aging. Here, we have mapped two types of oxidative DNA damage, oxidized guanines produced by hydrogen peroxide and oxidized thymines created by potassium permanganate, at a single-base resolution. 8-Oxo-guanine occurs strictly dependent on the G/C sequence context and shows a pronounced peak at transcription start sites (TSSs). We determined the trinucleotide sequence pattern of guanine oxidation. This pattern shows high similarity to the cancer-associated single-base substitution signatures SBS18 and SBS36. SBS36 is found in colorectal cancers that carry mutations in , encoding a repair enzyme that operates on 8-oxo-guanine mispairs. SBS18 is common in inflammation-associated upper gastrointestinal tract tumors including esophageal and gastric adenocarcinomas. Oxidized thymines induced by permanganate occur with a distinct dinucleotide specificity, 5'T-A/C, and are depleted at the TSS. Our data suggest that two cancer mutational signatures, SBS18 and SBS36, are caused by reactive oxygen species.

摘要

氧化 DNA 损伤与炎症、癌症和衰老有关。在这里,我们以单碱基分辨率绘制了两种类型的氧化 DNA 损伤:由过氧化氢产生的氧化鸟嘌呤和由高锰酸钾产生的氧化胸腺嘧啶。8-氧鸟嘌呤的产生严格依赖于 G/C 序列背景,并在转录起始位点(TSS)处呈现明显的峰值。我们确定了鸟嘌呤氧化的三核苷酸序列模式。该模式与癌症相关的单碱基替换特征 SBS18 和 SBS36 高度相似。SBS36 存在于携带编码修复酶的基因突变的结直肠癌中,该修复酶作用于 8-氧鸟嘌呤错配。SBS18 在炎症相关的上消化道肿瘤中很常见,包括食管和胃腺癌。锰酸钾诱导的氧化胸腺嘧啶以独特的二核苷酸特异性 5'T-A/C 发生,在 TSS 处耗尽。我们的数据表明,两种癌症突变特征 SBS18 和 SBS36 是由活性氧引起的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/672a/9166614/18aa9d21460e/sciadv.abn3815-f1.jpg

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