Literature DB >> 16207638

Recommendations for the interpretation of renal tubule proliferative lesions occurring in rat kidneys with advanced chronic progressive nephropathy (CPN).

Gordon C Hard1, John Curtis Seely.   

Abstract

There is little guidance in the literature on the spectrum of proliferative tubule lesions in the kidneys of aging rats affected with spontaneously occurring, chronic progressive nephropathy (CPN), or their interpretation. Through accessing 2-year carcinogenicity studies in male F344 rats held in the Archives of the National Toxicology Program, NIEHS, a large number of cases of advanced CPN have been surveyed histopathologically for proliferative tubule lesions, and an attempt made to provide guidelines for discrimination of lesions common to the CPN process, from those representing precursors of neoplasia. Several proliferative lesions were identified as common in advanced CPN with no apparent evidence supporting a role in renal tubule carcinogenesis. It is recommended that these lesions be viewed generically as CPN tubule profiles, and not recorded separately from the diagnosis of CPN. Criteria were developed to distinguish these CPN-associated lesions from atypical tubule hyperplasia, a precursor of adenoma, both of which were also represented in this survey of advanced CPN.

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Year:  2005        PMID: 16207638     DOI: 10.1080/01926230500299716

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  4 in total

1.  Spontaneous occurrence of a distinctive renal tubule tumor phenotype in rat carcinogenicity studies conducted by the national toxicology program.

Authors:  Gordon C Hard; John Curtis Seely; Grace E Kissling; Laura J Betz
Journal:  Toxicol Pathol       Date:  2008-04-25       Impact factor: 1.902

2.  Physiologically based pharmacokinetic model for ethyl tertiary-butyl ether and tertiary-butyl alcohol in rats: Contribution of binding to α2u-globulin in male rats and high-exposure nonlinear kinetics to toxicity and cancer outcomes.

Authors:  Susan J Borghoff; Caroline Ring; Marcy I Banton; Teresa L Leavens
Journal:  J Appl Toxicol       Date:  2016-11-24       Impact factor: 3.446

3.  Short-term Low-Dose mTORC1 Inhibition in Aged Rats Counter-Regulates Age-Related Gene Changes and Blocks Age-Related Kidney Pathology.

Authors:  Tea Shavlakadze; Jiang Zhu; Sharon Wang; Weihua Zhou; Bret Morin; Marc A Egerman; Lin Fan; Yanqun Wang; Oleg Iartchouk; Angelika Meyer; Reginald A Valdez; Joan B Mannick; Lloyd B Klickstein; David J Glass
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2018-06-14       Impact factor: 6.053

Review 4.  Confounders for kidney carcinogenesis in rodent cancer bioassays.

Authors:  Gordon C Hard
Journal:  J Toxicol Pathol       Date:  2021-10-14       Impact factor: 1.628

  4 in total

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