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1,3-Butadiene, CML and the t(9:22) translocation: A reality check
Richard J Albertini1, Elizabeth W Carter2, Janice A Nicklas3
1Department of Pathology, University of Vermont, Burlington, VT, United States.
Chemico-Biological Interactions
|May 24, 2015
Summary
Ionizing radiation can induce Philadelphia chromosome translocations linked to chronic myeloid leukemia (CML) in human cells, but at low frequencies. This finding establishes a positive control for future studies investigating chemical exposures, such as 1,3-butadiene, and their potential CML association.
Area of Science:
- Toxicology
- Genetics
- Oncology
Background:
- Epidemiological studies suggest a link between 1,3-butadiene exposure and chronic myeloid leukemia (CML).
- CML is associated with ionizing radiation, which can induce the t(9:22) translocation (Philadelphia chromosome).
- Chemical induction of the Philadelphia chromosome has not been demonstrated, questioning chemical links to CML.
Purpose of the Study:
- To establish a positive control for in vitro studies investigating the CML-associated t(9:22) translocation.
- To assess the capacity of ionizing radiation to induce pathogenic translocations in a human myeloid cell line.
- To determine conditions for future studies on 1,3-butadiene metabolites and their potential to induce CML-associated translocations.
Main Methods:
- Utilized ionizing radiation as a positive control agent.
- Exposed a human myeloid cell line in vitro.
- Quantified the induction frequency of t(9:22) translocations.
Main Results:
- Ionizing radiation successfully induced pathogenic t(9:22) translocations in the human myeloid cell line.
- The induction frequency of these translocations by ionizing radiation was observed to be low.
- Established conditions necessary for future investigations into 1,3-butadiene's genotoxic effects.
Conclusions:
- Ionizing radiation serves as a viable, albeit low-frequency, positive control for inducing CML-associated translocations in vitro.
- The established methodology provides a framework for testing the genotoxicity of chemical exposures, like 1,3-butadiene metabolites.
- Further research is warranted to explore the potential of 1,3-butadiene metabolites in inducing CML-associated translocations.

