Essential metals play important roles
in maintaining cellular homeostasis,
but the effects of their interaction with the environmental pollutants
are still not very well-known in human subjects. The aim of this study
was to evaluate the roles of essential metals and their interactions
with polycyclic aromatic hydrocarbons (PAHs) on chromosome damage,
an early carcinogenic event. A total of 1245 male workers were included
in this study and the levels of 11 urinary essential metals, 12 urinary
PAH metabolites, plasma concentrations of benzo[a]pyrene-r-7,t-8,t-9,c-10-tetrahydotetrol-albumin
(BPDE-Alb) adducts, and lymphocyte micronucleus (MN) frequencies were
monitored. We found that zinc (Zn), selenium (Se), and strontium (Sr)
have significant inverse dose–response relationships with MN
frequencies (all P < 0.05). Furthermore, the protective
roles of Zn, Se, and Sr were mainly shown among subjects with high
levels of BPDE-Alb adducts. Significant effect modification of BPDE-Alb
adducts on the associations of Zn, Se, and Sr with MN frequencies
was observed (all Pinteraction < 0.05).
Our study showed evidence that Zn, Se, and Sr play protective roles
in reducing chromosome damage, and these effects can be modified by
PAH exposure levels. These findings add potential evidence for the
preventive effects of Zn, Se, and Sr against carcinogenesis in human
subjects.