[Polymorphism of XRCC1 and chromosome damage in workers occupationally exposed to benzene]

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2012 Jun;30(6):423-7.
[Article in Chinese]

Abstract

Objective: To explore the relationship between the polymorphisms of DNA repair gene (XRCC1 194, 280 and 399) and the chromosomal damage induced by benzene.

Methods: The chromosomal damage of the peripheral lymphocytes in 459 workers occupationally exposed to benzene and 88 non-exposed controls were detected with cytokinesis-block micronucleus (CBMN) assay. PCR-RFLP technique was used to measure polymorphisms in XRCC1 194, 280 and 399.

Results: It was found that the MN frequency (2.12‰ ± 1.88‰) of the exposed group was significantly higher than that (1.19‰ ± 1.68‰) of the control group (P < 0.05), in the exposed group, the MN frequency (3.00‰ ± 2.76‰) of older workers (> 35 years) was significantly higher than that (2.02‰ ± 1.71‰) of younger workers (≤ 35 years) (P < 0.05). The effect of genetic polymorphisms of XRCC1 on CBMN was not found. The haplotypes AAA/BAA, AAB/AAB, ABA/ABA, ABB/ABB could associated with the increased frequencies of total micronucleus (P < 0.05).

Conclusion: Benzene exposure could result in chromosome damage. Age of workers and diplotypes of XRCC1 could associated with chromosomal damage induced by benzene.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Benzene / adverse effects*
  • DNA Damage / drug effects*
  • DNA Damage / genetics
  • DNA-Binding Proteins / genetics*
  • Humans
  • Micronuclei, Chromosome-Defective
  • Micronucleus Tests
  • Occupational Exposure*
  • Polymorphism, Single Nucleotide
  • X-ray Repair Cross Complementing Protein 1
  • Young Adult

Substances

  • DNA-Binding Proteins
  • X-ray Repair Cross Complementing Protein 1
  • XRCC1 protein, human
  • Benzene