Literature DB >> 9864088

Time- and dose-dependent development of potassium bromate-induced tumors in male Fischer 344 rats.

D C Wolf1, L M Crosby, M H George, S R Kilburn, T M Moore, R T Miller, A B DeAngelo.   

Abstract

Potassium bromate (KBrO3) is a rodent carcinogen and a nephro- and neurotoxicant in humans. KBrO3 is used in cosmetics and food products and is a by-product of water disinfection by ozonization. KBrO3 is carcinogenic in the rat kidney, thyroid, and mesothelium and is a renal carcinogen in the male mouse. The present study was designed to investigate the relationship of time and dose to bromate-induced tumors in male Fischer 344 (F344) rats and to provide some insight into the development of these tumors. KBrO3 was dissolved in drinking water at nominal concentrations of 0, 0.02, 0.1, 0.2, and 0.4 g/L and administered to male F344 rats as the sole water source for 12, 26, 52, 78, or 100 wk. Renal cell tumors were present after 52 wk of treatment only in the high-dose group. Mesotheliomas developed after 52 wk of treatment on the tunica vaginalis. Mesotheliomas were present at sites other than the testicle after 78 wk of treatment, indicating that their origin was the testicular tunic. Thyroid follicular tumors were present as early as 26 wk in 1 rat each from the 0.1- and 0.2-g/L groups. The present study can be used as a basis for the determination of dose-time relationships of tumor development for a better understanding of KBrO3-induced cancer.

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Year:  1998        PMID: 9864088     DOI: 10.1177/019262339802600602

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


  9 in total

1.  Potassium bromate-induced kidney damage in rats and the effect of gum acacia thereon.

Authors:  Badreldin H Ali; Mohammed Al Za'abi; Turan Karaca; Yousuf Al Suleimani; Khalid A Al Balushi; Priyadarsini Manoj; Mohammed Ashique; Abderrahim Nemmar
Journal:  Am J Transl Res       Date:  2018-01-15       Impact factor: 4.060

2.  Toxicity and carcinogenicity of the water disinfection byproduct, dibromoacetic acid, in rats and mice.

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3.  Squalene deters drivers of RCC disease progression beyond VHL status.

Authors:  Karthikeyan Rajamani; Somasundaram S Thirugnanasambandan; Chidambaram Natesan; Sethupathy Subramaniam; Balasubramanian Thangavel; Natarajan Aravindan
Journal:  Cell Biol Toxicol       Date:  2020-11-21       Impact factor: 6.691

4.  New aspects in deriving health-based guidance values for bromate in swimming pool water.

Authors:  C Röhl; M Batke; G Damm; A Freyberger; T Gebel; U Gundert-Remy; J G Hengstler; A Mangerich; A Matthiessen; F Partosch; T Schupp; K M Wollin; H Foth
Journal:  Arch Toxicol       Date:  2022-04-06       Impact factor: 6.168

5.  Bromate-induced Changes in p21 DNA Methylation and Histone Acetylation in Renal Cells.

Authors:  Ramya T Kolli; Travis C Glenn; Bradley T Brown; Sukhneeraj P Kaur; Lillie M Barnett; Lawrence H Lash; Brian S Cummings
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Review 6.  Choosing The Right Animal Model for Renal Cancer Research.

Authors:  Paweł Sobczuk; Anna Brodziak; Mohammed Imran Khan; Stuti Chhabra; Michał Fiedorowicz; Marlena Wełniak-Kamińska; Kamil Synoradzki; Ewa Bartnik; Agnieszka Cudnoch-Jędrzejewska; Anna M Czarnecka
Journal:  Transl Oncol       Date:  2020-02-22       Impact factor: 4.243

7.  Epigenetic changes in p21 expression in renal cells after exposure to bromate.

Authors:  N E Scholpa; X Zhang; R T Kolli; B S Cummings
Journal:  Toxicol Sci       Date:  2014-07-11       Impact factor: 4.849

8.  Oxidative damage to macromolecules in the thyroid - experimental evidence.

Authors:  Małgorzata Karbownik-Lewińska; Agnieszka Kokoszko-Bilska
Journal:  Thyroid Res       Date:  2012-12-27

9.  Kidney toxicogenomics of chronic potassium bromate exposure in f344 male rats.

Authors:  David R Geter; William O Ward; Geremy W Knapp; Anthony B Deangelo; Jessica A Rubis; Russell D Owen; James W Allen; Don A Delker
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  9 in total

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