小RNA
癌变
肺癌
调解
微核
泊松回归
泌尿系统
置信区间
肿瘤科
肺
内科学
生理学
生物
医学
胃肠病学
内分泌学
癌症研究
癌症
遗传学
微核试验
人口
毒性
基因
法学
环境卫生
政治学
作者
Weilin Chen,Wenshan Fu,Qifei Deng,Yangkai Li,Ke Wang,Yansen Bai,Xiulong Wu,Guyanan Li,Gege Wang,Jiao Huang,Meian He,Xiaomin Zhang,Tangchun Wu,Sheng Wei,Huan Guo
标识
DOI:10.1016/j.envint.2018.11.020
摘要
OBJECTIVE: This study aimed to investigate the associations of multiple metals with chromosome damage, and further explore the mediation roles of microRNAs (miRNAs) and their potentials in lung cancer. METHODS: We determined the urinary levels of 23 metals, lymphocytic micronucleus (MN) frequency, and ten candidate miRNAs in plasma among 365 healthy workers. Poisson and linear regression models were conducted to analyze the associations of urinary metals with MN frequency and miRNAs, respectively. The mediation effects of miRNAs on the metal-MN frequency associations were assessed by causal mediation analysis. Additionally, the levels of effective metal and miRNAs were measured in 43 pair-wised tumor and normal lung tissues. RESULTS: = 0.002 and 0.004, respectively). Besides, a doubling in titanium was associated with a separate 53.4% and 47.2% decreased miR-24-3p and miR-28-5p expression in normal lung tissues. Lower titanium but higher levels of miR-24-3p and miR-28-5p were shown in tumor than normal tissues of lung squamous cell carcinoma patients (all p < 0.05). CONCLUSIONS: Our study proposed the negative associations of titanium with chromosome damage and lung cancer, and highlighted the mediating roles of miR-24-3p and miR-28-5p. Further investigations are warranted to validate these associations and uncover the underlying mechanisms.
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