HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Global and MGMT promoter hypomethylation independently associated with genomic instability of lymphocytes in subjects exposed to high-dose polycyclic aromatic hydrocarbon.

Abstract
Global hypomethylation, gene-specific methylation, and genome instability are common events in tumorigenesis. To date, few studies have examined the aberrant DNA methylation patterns in coke oven workers, who are highly at risk of lung cancer by occupational exposure to polycyclic aromatic hydrocarbons (PAHs). We recruited 82 PAH-exposed workers and 62 unexposed controls, assessed exposure levels by urinary 1-hydroxypyrene, and measured genetic damages by comet assay, bleomycin sensitivity, and micronucleus assay. The PAHs in coke oven emissions (COE) were estimated based on toxic equivalency factors. We used bisulfite-PCR pyrosequencing to quantitate DNA methylation in long interspersed nuclear element-1 (LINE-1) and O(6)-methylguanine-DNA methyltransferase (MGMT). Further, the methylation alteration was also investigated in COE-treated human bronchial epithelial (16HBE) cells. We found there are higher levels of PAHs in COE. Among PAH-exposed workers, LINE-1 and MGMT methylation levels (with CpG site specificity) were significantly lowered. LINE-1, MGMT, and its hot CpG site-specific methylation were negatively correlated with urinary 1-hydroxypyrene levels (r = -0.329, p < 0.001; r = -0.164, p = 0.049 and r = -0.176, p = 0.034, respectively). In addition, LINE-1 methylation was inversely associated with comet tail moment and micronucleus frequency, and a significant increase of micronucleus in low MGMT methylation group. In vitro study revealed that treatment of COE in 16HBE cells resulted in higher production of BPDE-DNA adducts, LINE-1 hypomethylation, hypomethylation, and suppression of MGMT expression. These findings suggest hypomethylation of LINE-1 and MGMT promoter could be used as markers for PAHs exposure and merit further investigation.
AuthorsHuawei Duan, Zhini He, Junxiang Ma, Bo Zhang, Zhiguo Sheng, Ping Bin, Juan Cheng, Yong Niu, Haiyan Dong, Han Lin, Yufei Dai, Benzhan Zhu, Wen Chen, Yongmei Xiao, Yuxin Zheng
JournalArchives of toxicology (Arch Toxicol) Vol. 87 Issue 11 Pg. 2013-2022 (Nov 2013) ISSN: 1432-0738 [Electronic] Germany
PMID23543013 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers
  • Mutagens
  • Polycyclic Compounds
  • Pyrenes
  • Sulfites
  • Steel
  • O(6)-Methylguanine-DNA Methyltransferase
  • 1-hydroxypyrene
  • hydrogen sulfite
Topics
  • Adult
  • Biomarkers
  • Blotting, Western
  • Cells, Cultured
  • China
  • Chromosomal Instability (drug effects)
  • Comet Assay
  • DNA Damage
  • DNA Methylation
  • Genomic Instability (drug effects)
  • Humans
  • Lymphocytes (physiology)
  • Male
  • Metallurgy
  • Methylation
  • Mutagens (toxicity)
  • O(6)-Methylguanine-DNA Methyltransferase (metabolism)
  • Occupational Exposure
  • Polycyclic Compounds (toxicity)
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic (physiology)
  • Pyrenes (urine)
  • Steel
  • Sulfites (pharmacology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: