Qiao Rong, Li Mengxia, Zhong Runbo, Wei Yujie, Wang Jun, Zhang Zheng, Wang Ling, Xu Tian, Wang Yue, Dai Liping, Gu Wanjian, Han Baohui, Yang Rongxi
Department of Pulmonary Medicine, Shanghai Chest Hospital, Shanghai Jiaotong University, Shanghai, 200030, People's Republic of China.
Department of Epidemiology and Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, 210000, People's Republic of China.
Cancer Manag Res. 2021 Oct 15;13:7919-7927. doi: 10.2147/CMAR.S329629. eCollection 2021.
Lung cancer (LC) brings great burden to the society worldwide. Exploring novel biomarkers in vitro for the early detection of LC would be of great importance.
We measured DNA methylation levels of 21 CpG sites within Patatin-like phospholipase domain containing 2 () gene in the peripheral blood of 168 early-stage LC cases (94.0% LC at stage I) and 187 age- and gender-matched cancer-free controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using logistic regression adjusted for covariates. Non-parametric tests were applied for the comparisons of stratified groups.
Hypomethylation of PNPLA2_CpG_8,10 and hypermethylation of PNPLA2_CpG_9 were correlated to the early-stage LC with the ORs of 1.44 (95% CI: 1.06-1.96, = 0.018) and 0.82 (95% CI: 0.69-0.98, = 0.029), respectively. The associations were still significant for the very early-stage LC patients (stage I). Further gender- and age-stratified analyses indicated that the association between hypomethylation of PNPLA2_CpG_8,10 and LC existed only in females and in subjects younger than 55 years. In addition, the association between LC and hypermethylation of PNPLA2_CpG_6 and PNPLA2_CpG_9 was also observed in the younger population.
Taken together, our study has proved the hypothesis that the altered methylation in the peripheral blood may be correlated with the burden of cancer at an early stage. Here, we find a novel association between blood-based aberrant methylation and LC at a very early stage and particularly for women at a younger age.
肺癌给全球社会带来了巨大负担。探索用于肺癌早期检测的新型体外生物标志物具有重要意义。
我们测量了168例早期肺癌病例(94.0%为I期肺癌)和187例年龄及性别匹配的无癌对照者外周血中含Patatin样磷脂酶结构域2()基因内21个CpG位点的DNA甲基化水平。使用经协变量调整的逻辑回归计算优势比(OR)和95%置信区间(CI)。应用非参数检验对分层组进行比较。
PNPLA2_CpG_8,10的低甲基化和PNPLA2_CpG_9的高甲基化与早期肺癌相关,OR分别为1.44(95%CI:1.06 - 1.96, = 0.018)和0.82(95%CI:0.69 - 0.98, = 0.029)。对于极早期肺癌患者(I期),这种关联仍然显著。进一步按性别和年龄分层分析表明,PNPLA2_CpG_8,10的低甲基化与肺癌之间的关联仅存在于女性和年龄小于55岁的受试者中。此外,在较年轻人群中也观察到肺癌与PNPLA2_CpG_6和PNPLA2_CpG_9的高甲基化之间的关联。
综上所述,我们的研究证实了外周血中甲基化改变可能与癌症早期负担相关的假设。在此,我们发现了基于血液的异常甲基化与极早期肺癌之间的新型关联,尤其是对于年轻女性。