Association of GSTT1 null, XPD 751 CC and XPC 939 CC genotypes with increased levels of genomic damage among hospital pathologists

Biomarkers. 2017 Sep;22(6):557-565. doi: 10.1080/1354750X.2017.1322147. Epub 2017 May 4.

Abstract

Context: Hospital workers are at risk for genotoxic damage following occupationally exposure to xenobiotics. Pathologists are exposed to chemicals during their use in health care environments, particularly throughout inhalation of airborne agents, absorption through skin or contact with the patient's body fluids.

Objective: We evaluated the level of genomic damage in a sample of 61 hospital pathologists (occupationally exposed to antineoplastic drugs and sterilizing agents) and 60 control subjects.

Materials and methods: Lymphocytes were analyzed by SCEs and CAs assays and genotyped for GSTT1, GSTM1, CYP1A1 Ile/Val, XPD (A751C) and XPC (A939C) gene polymorphisms.

Results: Pathologists showed significantly higher frequencies of SCEs and CAs with respect to control subjects. GSTT1 null genotype was found to be associated with higher SCEs and CAs frequencies, whereas XPD 751 CC and XPC 939 CC genotypes only with a higher level of SCEs.

Discussion and conclusions: The SCEs and CAs results are consistent with other published data, placing hospital workers as a category at risk for genotoxic damage caused by chronic exposure to xenobiotics. The higher levels of cytogenetic damage observed among GSTT1 null, XPD 751 and XPC 939 CC homozygote subjects confirm the importance of the genetic polymorphisms analysis associated to genotoxicological studies.

Keywords: BER; NER; SCE; chromosomal aberration; genetic polymorphisms; glutathione-S-transferase.

MeSH terms

  • Adult
  • Antineoplastic Agents
  • Case-Control Studies
  • DNA Damage*
  • DNA-Binding Proteins / genetics*
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Genotype*
  • Glutathione Transferase / genetics*
  • Humans
  • Lymphocytes
  • Male
  • Middle Aged
  • Mutagens / adverse effects
  • Occupational Exposure / analysis*
  • Pathologists*
  • Sterilization
  • Xenobiotics / adverse effects
  • Xeroderma Pigmentosum Group D Protein / genetics*
  • Young Adult

Substances

  • Antineoplastic Agents
  • DNA-Binding Proteins
  • Mutagens
  • Xenobiotics
  • XPC protein, human
  • glutathione S-transferase T1
  • Glutathione Transferase
  • Xeroderma Pigmentosum Group D Protein
  • ERCC2 protein, human