Use of cell proliferation data in modeling urinary bladder carcinogenesis

S. M. Cohen, L. B. Ellwein

Research output: Contribution to journalArticle

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Abstract

A multistage, probabilistic, biologically based model of carcinogenesis has been developed involving qualitative and quantitative aspects of the process. A chemical can affect the risk of cancer by directly damaging DNA and/or increasing the number of cell divisions during which errors in DNA replication can occur. Based on this model, carcinogens are classified as genotoxic versus nongenotoxic; nongenotoxic chemicals are further divided on the basis of whether or not they act through a specific cell receptor. Nongenotoxic compounds, particularly those acting through a nonreceptor mechanism, are likely to have dose and/or species-specific thresholds. This classification also implies the existence of chemicals that will be carcinogenic at high doses in animal models, but because of dose and/or mechanistic considerations, will not be carcinogenic to humans at levels of exposure. N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide (FANFT) and 2-acetylaminofluorene (AAF) are classical genotoxic bladder carcinogens that also cause proliferative effects at higher doses. Although there is an apparent no-effect level for the urinary bladder carcinogenicity of these two compounds at low doses, in reality, DNA adducts form at these low levels, and it is likely that there is a cancer effect (no threshold), but it is below the level of detection of the bioassay. These conclusions are based on studies involving multiple doses and time points in rodents, including results from the ED01. Pellets implanted directly into the rodent bladder lumen or calculi formed in the urine as a result of an administered chemical cause abrasion of the urothelium, and a marked increase in cell proliferation and cell number, and ultimately tumors. A threshold is readily definable based on physiologic, chemical, and pharmacokinetic considerations. Sodium saccharin also produces bladder cancer at high doses in rats, particularly males, if it is administered beginning at birth or earlier. The mechanism appears to be related to the formation of a silicate precipitate and/or crystals formed in the rat urine, which act as abrasives or cytotoxic materials, leading to increased cell proliferation and ultimately tumors. Numerous other sodium salts have similar effects. This effect is not observed in the mouse, hamster, or monkey, and epidemiological evidence suggests that it does not occur in humans. Thus, for sodium saccharin, even in the susceptible species, the rat, there appears to be a dose threshold, and extrapolation to humans appears inappropriate based on mechanistic considerations.

Original languageEnglish (US)
Pages (from-to)111-113
Number of pages3
JournalEnvironmental Health Perspectives
Volume101
Issue numberSUPPL. 5
StatePublished - Dec 1 1993

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ASJC Scopus subject areas

  • Public Health, Environmental and Occupational Health
  • Health, Toxicology and Mutagenesis

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