• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

口腔细菌感染对宿主细胞DNA损伤反应的影响。

The effect of oral bacterial infection on DNA damage response in host cells.

作者信息

Oh Jung-Min, Kim Hongtae

机构信息

Department of Oral Biochemistry, Dental and Life Science Institute, School of Dentistry, Pusan National University Yangsan 50612, Republic of Korea.

Department of Life Science in Dentistry, School of Dentistry, Pusan National University Yangsan 50612, Republic of Korea.

出版信息

Am J Cancer Res. 2023 Jul 15;13(7):3157-3168. eCollection 2023.

PMID:37559975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10408462/
Abstract

Maintaining and transferring intact genomes from one generation to another plays a pivotal role in all living organisms. DNA damage caused by numerous endogenous and exogenous factors must be adequately repaired, as unrepaired and accumulated DNA mutations can cause severe deleterious effects, such as cell death and cancer. To prevent adverse consequences, cells have established DNA damage response mechanisms that address different forms of DNA damage, including DNA double-strand breaks, mismatches, nucleotide excision, and base excision. Among several sources of exogenous DNA damage, bacterial infections cause inflammation in the host, generating reactive oxygen species (ROS) and causing oxidative DNA damage. Recent studies have revealed the importance of the oral microbiome in inflammation and several systemic host diseases. Dysbiosis of oral bacteria can induce chronic inflammation, which enhances ROS-induced DNA damage, and improperly repaired damage can lead to carcinogenesis. This review describes the various DNA repair pathways that are affected by chronic inflammation and the discovery of the DNA damage response induced by oral bacteria such as and .

摘要

将完整的基因组从一代维持并传递到下一代在所有生物中都起着关键作用。由众多内源性和外源性因素导致的DNA损伤必须得到充分修复,因为未修复和积累的DNA突变会造成严重的有害影响,如细胞死亡和癌症。为防止出现不良后果,细胞建立了DNA损伤应答机制,以应对不同形式的DNA损伤,包括DNA双链断裂、错配、核苷酸切除和碱基切除。在多种外源性DNA损伤来源中,细菌感染会在宿主体内引发炎症,产生活性氧(ROS)并造成氧化性DNA损伤。最近的研究揭示了口腔微生物群在炎症和几种全身性宿主疾病中的重要性。口腔细菌的生态失调可诱发慢性炎症,这会加剧ROS诱导的DNA损伤,而修复不当的损伤可能导致癌变。本综述描述了受慢性炎症影响的各种DNA修复途径,以及诸如[具体细菌名称]等口腔细菌诱导的DNA损伤应答的发现。

相似文献

1
The effect of oral bacterial infection on DNA damage response in host cells.口腔细菌感染对宿主细胞DNA损伤反应的影响。
Am J Cancer Res. 2023 Jul 15;13(7):3157-3168. eCollection 2023.
2
The Pivotal Role of DNA Repair in Infection Mediated-Inflammation and Cancer.DNA修复在感染介导的炎症和癌症中的关键作用。
Front Microbiol. 2018 Apr 11;9:663. doi: 10.3389/fmicb.2018.00663. eCollection 2018.
3
NOX1/2 activation in human gingival fibroblasts by Fusobacterium nucleatum facilitates attachment of Porphyromonas gingivalis.具核梭杆菌激活人牙龈成纤维细胞中的NOX1/2促进牙龈卟啉单胞菌的黏附。
Arch Microbiol. 2016 Aug;198(6):573-83. doi: 10.1007/s00203-016-1223-7. Epub 2016 Apr 12.
4
Immunological Pathways Triggered by and : Therapeutic Possibilities?炎症小体激活途径及其相关治疗策略
Mediators Inflamm. 2019 Jun 24;2019:7241312. doi: 10.1155/2019/7241312. eCollection 2019.
5
Fusobacterium nucleatum mediates endothelial damage and increased permeability following single species and polymicrobial infection.具核梭杆菌介导单一菌种和混合菌种感染后内皮细胞损伤和通透性增加。
J Periodontol. 2022 Sep;93(9):1421-1433. doi: 10.1002/JPER.21-0671. Epub 2022 Jun 28.
6
Molecular mechanisms of DNA damage and repair: progress in plants.DNA损伤与修复的分子机制:植物研究进展
Crit Rev Biochem Mol Biol. 2001;36(4):337-97. doi: 10.1080/20014091074219.
7
Differential involvement of the canonical and noncanonical inflammasomes in the immune response against infection by the periodontal bacteria and .经典和非经典炎性小体在针对牙周细菌感染的免疫反应中的不同参与情况。
Curr Res Microb Sci. 2021 Feb 23;2:100023. doi: 10.1016/j.crmicr.2021.100023. eCollection 2021 Dec.
8
Mouse model of experimental periodontitis induced by Porphyromonas gingivalis/Fusobacterium nucleatum infection: bone loss and host response.牙龈卟啉单胞菌/具核梭杆菌感染诱导的实验性牙周炎小鼠模型:骨质流失与宿主反应
J Clin Periodontol. 2009 May;36(5):406-10. doi: 10.1111/j.1600-051X.2009.01393.x.
9
Porphyromonas gingivalis outer membrane vesicles inhibit the invasion of Fusobacterium nucleatum into oral epithelial cells by downregulating FadA and FomA.牙龈卟啉单胞菌外膜囊泡通过下调 FadA 和 FomA 抑制核梭杆菌侵入口腔上皮细胞。
J Periodontol. 2022 Apr;93(4):515-525. doi: 10.1002/JPER.21-0144. Epub 2021 Oct 5.
10
Label-free quantitative proteomic analysis of the oral bacteria Fusobacterium nucleatum and Porphyromonas gingivalis to identify protein features relevant in biofilm formation.口腔细菌福赛斯坦纳菌和牙龈卟啉单胞菌的无标记定量蛋白质组学分析,以鉴定与生物膜形成相关的蛋白质特征。
Anaerobe. 2021 Dec;72:102449. doi: 10.1016/j.anaerobe.2021.102449. Epub 2021 Sep 17.

引用本文的文献

1
Bidirectional Interaction Between Chronic Kidney Disease and Infection Drives Inflammation and Immune Dysfunction.慢性肾脏病与感染之间的双向相互作用驱动炎症和免疫功能障碍。
J Immunol Res. 2025 Apr 17;2025:8355738. doi: 10.1155/jimr/8355738. eCollection 2025.
2
Gallium-based metal-organic frameworks with antibacterial and anti-inflammatory properties for oral health protection.具有抗菌和抗炎特性的镓基金属有机框架用于口腔健康保护。
Heliyon. 2024 May 22;10(11):e31788. doi: 10.1016/j.heliyon.2024.e31788. eCollection 2024 Jun 15.
3
A Review of the Repair of DNA Double Strand Breaks in the Development of Oral Cancer.口腔癌发生过程中 DNA 双链断裂修复的研究综述
Int J Mol Sci. 2024 Apr 7;25(7):4092. doi: 10.3390/ijms25074092.

本文引用的文献

1
Fusobacterium nucleatum impairs DNA mismatch repair and stability in patients with squamous cell carcinoma of the head and neck.具核梭杆菌损害头颈部鳞状细胞癌患者的 DNA 错配修复和稳定性。
Cancer. 2022 Sep 1;128(17):3170-3184. doi: 10.1002/cncr.34338. Epub 2022 Jul 5.
2
Crosstalk between different DNA repair pathways for DNA double strand break repairs.不同 DNA 修复途径之间的串扰用于修复 DNA 双链断裂。
Mutat Res Genet Toxicol Environ Mutagen. 2022 Jan;873:503438. doi: 10.1016/j.mrgentox.2021.503438. Epub 2021 Dec 15.
3
The Oral Microbiome and Cancer.口腔微生物群与癌症
Front Immunol. 2020 Oct 23;11:591088. doi: 10.3389/fimmu.2020.591088. eCollection 2020.
4
infection correlates with two types of microsatellite alterations in colorectal cancer and triggers DNA damage.感染与结直肠癌中的两种微卫星改变相关,并引发DNA损伤。
Gut Pathog. 2020 Sep 29;12:46. doi: 10.1186/s13099-020-00384-3. eCollection 2020.
5
FadA promotes DNA damage and progression of Fusobacterium nucleatum-induced colorectal cancer through up-regulation of chk2.FadA 通过上调 chk2 促进具核梭杆菌诱导的结直肠癌的 DNA 损伤和进展。
J Exp Clin Cancer Res. 2020 Sep 29;39(1):202. doi: 10.1186/s13046-020-01677-w.
6
Defining the mutation signatures of DNA polymerase θ in cancer genomes.确定癌症基因组中DNA聚合酶θ的突变特征。
NAR Cancer. 2020 Sep;2(3):zcaa017. doi: 10.1093/narcan/zcaa017. Epub 2020 Aug 27.
7
Mechanistic basis for microhomology identification and genome scarring by polymerase theta.聚合酶 θ 进行微同源识别和基因组疤痕形成的机制基础。
Proc Natl Acad Sci U S A. 2020 Apr 14;117(15):8476-8485. doi: 10.1073/pnas.1921791117. Epub 2020 Mar 31.
8
LPS-induced premature osteocyte senescence: Implications in inflammatory alveolar bone loss and periodontal disease pathogenesis.脂多糖诱导的成骨细胞过早衰老:对炎症性牙槽骨丧失和牙周病发病机制的影响
Bone. 2020 Mar;132:115220. doi: 10.1016/j.bone.2019.115220. Epub 2020 Jan 2.
9
Caused DNA Damage and Promoted Cell Proliferation by the / Pathway in Oral Cancer Cells.通过 / 途径导致口腔癌细胞的 DNA 损伤和促进细胞增殖。
DNA Cell Biol. 2020 Jan;39(1):144-151. doi: 10.1089/dna.2019.5064. Epub 2019 Nov 25.
10
Oral microbiome: Unveiling the fundamentals.口腔微生物群:揭示基本原理。
J Oral Maxillofac Pathol. 2019 Jan-Apr;23(1):122-128. doi: 10.4103/jomfp.JOMFP_304_18.