Department of Epidemiology, Brown University, Providence, Rhode Island.
Department of Public Health and Community Medicine, Tufts University School of Medicine, Tufts University, Boston, Massachusetts.
Cancer Epidemiol Biomarkers Prev. 2024 Oct 2;33(10):1339-1346. doi: 10.1158/1055-9965.EPI-24-0279.
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.
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.
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).
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.
Identifying biological pathways that link periodontal disease and lung cancer could provide new opportunities for lung cancer detection and prevention.
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。
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。
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)。
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。
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。