Systematic evaluation of the evidence base on ethyl tert-butyl ether and tert-butyl alcohol for carcinogenic potential in humans; lack of concern based on animal cancer studies and mechanistic data

Ethyl <i>tert</i>-butyl ether (ETBE), a fuel additive, and <i>tert</i>-butyl alcohol (TBA), a solvent and metabolite of ETBE and methyl <i>tert</i>-butyl ether (MTBE), may be encountered via inhalation, oral, or dermal exposure. This assessment evaluated the human carcinogenic hazard of ETBE and TBA by systematically reviewing available human, animal, and mechanistic data. No epidemiological studies were identified, and two standard cancer bioassays were available for each compound. Tumor responses were limited to low incidences at high exposure levels: liver tumors in male F344 rats, kidney tumors in male F344 rats, and thyroid tumors in female B6C3F1 mice exposed to ETBE or TBA, respectively. Mechanistic evidence was organized within the framework of the key characteristics of carcinogens (KCC) and established rodent non-genotoxic modes of action (MoAs) for the overall evaluation. Aside from supportive evidence for KCC2 (is genotoxic) and KCC10 (alters cell proliferation, death, or nutrient supply), mechanistic data across KCCs were sparse and inconsistent. Both substances lacked genotoxic activity with available data supporting non-genotoxic MoAs that are not relevant to humans. Overall, the evidence indicates little concern for a carcinogenic hazard of ETBE or TBA in humans.

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Journal
Current Research in Toxicology
Published
2025-11-11
DOI
https://doi.org/10.1016/j.crtox.2025.100270
Primary Topic
Carcinogens and Genotoxicity Assessment
Type
article
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article

Systematic evaluation of the evidence base on ethyl tert-butyl ether and tert-butyl alcohol for carcinogenic potential in humans; lack of concern based on animal cancer studies and mechanistic data

B. Rivera, Neepa Choksi, Allison Franzen, Susan J. Borghoff et al.
Current Research in Toxicology
Carcinogens and Genotoxicity Assessment
article

Systematic evaluation of the evidence base on ethyl tert-butyl ether and tert-butyl alcohol for carcinogenic potential in humans; lack of concern based on animal cancer studies and mechanistic data

B. Rivera, Neepa Choksi, Allison Franzen, Susan J. Borghoff, Léa Ikhlef, Seneca Fitch, James S. Bus, Erik Rushton
article en

Abstract

Ethyl <i>tert</i>-butyl ether (ETBE), a fuel additive, and <i>tert</i>-butyl alcohol (TBA), a solvent and metabolite of ETBE and methyl <i>tert</i>-butyl ether (MTBE), may be encountered via inhalation, oral, or dermal exposure. This assessment evaluated the human carcinogenic hazard of ETBE and TBA by systematically reviewing available human, animal, and mechanistic data. No epidemiological studies were identified, and two standard cancer bioassays were available for each compound. Tumor responses were limited to low incidences at high exposure levels: liver tumors in male F344 rats, kidney tumors in male F344 rats, and thyroid tumors in female B6C3F1 mice exposed to ETBE or TBA, respectively. Mechanistic evidence was organized within the framework of the key characteristics of carcinogens (KCC) and established rodent non-genotoxic modes of action (MoAs) for the overall evaluation. Aside from supportive evidence for KCC2 (is genotoxic) and KCC10 (alters cell proliferation, death, or nutrient supply), mechanistic data across KCCs were sparse and inconsistent. Both substances lacked genotoxic activity with available data supporting non-genotoxic MoAs that are not relevant to humans. Overall, the evidence indicates little concern for a carcinogenic hazard of ETBE or TBA in humans.

Current Research in ToxicologyVol. 10
Exponent (United States) (US)
Openalex Percentile: Top 59%
Carcinogens and Genotoxicity Assessment
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Systematic evaluation of the evidence base on ethyl tert-butyl ether and tert-butyl alcohol for carcinogenic potential in humans; lack of concern based on animal cancer studies and mechanistic data — B. Rivera, Neepa Choksi, et al. · Current Research in Toxicology (2025) | TGRS Research Map | TGRS