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本文引用的文献

1
Epigenome-wide association study using peripheral blood leukocytes identifies genomic regions associated with periodontal disease and edentulism in the Atherosclerosis Risk in Communities study.采用外周血白细胞进行的表观基因组全基因组关联研究,在社区动脉粥样硬化风险研究中确定了与牙周病和无牙症相关的基因组区域。
J Clin Periodontol. 2023 Sep;50(9):1140-1153. doi: 10.1111/jcpe.13852. Epub 2023 Jul 18.
2
The Role of Zinc Finger Proteins in Various Oral Conditions.锌指蛋白在各种口腔状况中的作用。
ScientificWorldJournal. 2022 Apr 15;2022:4612054. doi: 10.1155/2022/4612054. eCollection 2022.
3
Enhanced cell deconvolution of peripheral blood using DNA methylation for high-resolution immune profiling.利用 DNA 甲基化增强外周血的细胞去卷积,实现高分辨率免疫分析。
Nat Commun. 2022 Feb 9;13(1):761. doi: 10.1038/s41467-021-27864-7.
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Homeobox Genes in Cancers: From Carcinogenesis to Recent Therapeutic Intervention.癌症中的同源盒基因:从致癌作用到近期的治疗干预
Front Oncol. 2021 Oct 14;11:770428. doi: 10.3389/fonc.2021.770428. eCollection 2021.
5
Epigenome-wide scan identifies differentially methylated regions for lung cancer using pre-diagnostic peripheral blood.基于外周血的肺癌表观基因组全扫描鉴定出差异甲基化区域
Epigenetics. 2022 Apr;17(4):460-472. doi: 10.1080/15592294.2021.1923615. Epub 2021 May 19.
6
KRAB-ZFP Transcriptional Regulators Acting as Oncogenes and Tumor Suppressors: An Overview.KRAB-ZFP 转录因子作为癌基因和肿瘤抑制因子的作用:概述。
Int J Mol Sci. 2021 Feb 23;22(4):2212. doi: 10.3390/ijms22042212.
7
ZNF718, HOXA4, and ZFP57 are differentially methylated in periodontitis in comparison with periodontal health: Epigenome-wide DNA methylation pilot study.ZNF718、HOXA4 和 ZFP57 在牙周炎与牙周健康中的甲基化程度存在差异:全基因组 DNA 甲基化初步研究。
J Periodontal Res. 2021 Aug;56(4):710-725. doi: 10.1111/jre.12868. Epub 2021 Mar 4.
8
Local and systemic mechanisms linking periodontal disease and inflammatory comorbidities.牙周病与炎症性合并症相关的局部和全身机制。
Nat Rev Immunol. 2021 Jul;21(7):426-440. doi: 10.1038/s41577-020-00488-6. Epub 2021 Jan 28.
9
Methylation in Clusters and Its Applications in Cancer Therapy.簇状甲基化及其在癌症治疗中的应用。
Cells. 2020 Jul 3;9(7):1613. doi: 10.3390/cells9071613.
10
Disruption of Immune Homeostasis in Human Dendritic Cells via Regulation of Autophagy and Apoptosis by .通过 调控自噬和凋亡来破坏人树突状细胞的免疫稳态
Front Immunol. 2019 Sep 24;10:2286. doi: 10.3389/fimmu.2019.02286. eCollection 2019.

病例对照研究巢式 CLUE II 队列中牙周病的血白细胞 DNA 甲基化标志物与肺癌风险。

Blood Leukocyte DNA Methylation Markers of Periodontal Disease and Risk of Lung Cancer in a Case-Control Study Nested in the CLUE II Cohort.

机构信息

Department of Epidemiology, Brown University, Providence, Rhode Island.

Department of Public Health and Community Medicine, Tufts University School of Medicine, Tufts University, Boston, Massachusetts.

出版信息

Cancer Epidemiol Biomarkers Prev. 2024 Oct 2;33(10):1339-1346. doi: 10.1158/1055-9965.EPI-24-0279.

DOI:10.1158/1055-9965.EPI-24-0279
PMID:39093033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11446649/
Abstract

BACKGROUND

Periodontal disease and DNA methylation markers have separately been associated with lung cancer risk. Examining methylation levels at genomic regions previously linked to periodontal disease may provide insights on the link between periodontal disease and lung cancer.

METHODS

In a nested case-control study drawn from the CLUE II cohort, we measured DNA methylation levels in 208 lung cancer cases and 208 controls. We examined the association between 37 DNA-methylated 5'-C-phosphate-G-3' (CpG) sites at three genomic regions, homeobox 4 (HOXA4), zinc finger protein (ZFP57), and a long noncoding RNA gene located in Chr10 (ENSG00000231601), and lung cancer risk.

RESULTS

Statistically significant associations with lung cancer risk were observed for all 14 CpG sites from HOXA4 (OR ranging 1.41-1.62 for 1 SD increase in the DNA methylation level, especially within 15 years) and 1 CpG site on gene ENSG00000231601 (OR = 1.34 for 1 SD increase in the DNA methylation level). Although CpG sites on gene ZFP57 were not associated with lung cancer risk overall, statistically significant inverse associations were noted for six CpG sites when restricting follow-up to 15 years (OR = 0.73-0.77 for 1 SD increase in the DNA methylation level).

CONCLUSIONS

Key methylation levels associated with periodontal disease are also associated with lung cancer risk. For both HOXA4 and ZFP57, the associations were stronger within 15 years of follow-up, which suggest that, if causal, the impact of methylation is acting late in the natural history of lung cancer.

IMPACT

Identifying biological pathways that link periodontal disease and lung cancer could provide new opportunities for lung cancer detection and prevention.

摘要

背景

牙周病和 DNA 甲基化标记物分别与肺癌风险相关。检查与牙周病相关的基因组区域的甲基化水平可能会提供牙周病与肺癌之间联系的线索。

方法

在 CLUE II 队列中进行的巢式病例对照研究中,我们测量了 208 例肺癌病例和 208 例对照的 DNA 甲基化水平。我们检查了三个基因组区域(同源盒 4(HOXA4)、锌指蛋白(ZFP57)和位于 Chr10 上的长非编码 RNA 基因(ENSG00000231601)中 37 个 DNA 甲基化 5'-C-磷酸-G-3'(CpG)位点与肺癌风险之间的关联。

结果

HOXA4 中所有 14 个 CpG 位点(DNA 甲基化水平每增加 1 个标准差,肺癌风险比为 1.41-1.62,尤其是在 15 年内)和基因 ENSG00000231601 上的 1 个 CpG 位点(DNA 甲基化水平每增加 1 个标准差,OR = 1.34)与肺癌风险呈统计学显著相关。尽管基因 ZFP57 上的 CpG 位点总体上与肺癌风险无关,但在随访 15 年内限制随访时,六个 CpG 位点存在统计学显著的反向关联(DNA 甲基化水平每增加 1 个标准差,OR = 0.73-0.77)。

结论

与牙周病相关的关键甲基化水平也与肺癌风险相关。对于 HOXA4 和 ZFP57,在随访的 15 年内,关联更强,这表明,如果是因果关系,甲基化的影响在肺癌的自然史晚期发挥作用。

影响

确定将牙周病与肺癌联系起来的生物学途径可能为肺癌检测和预防提供新的机会。