Literature DB >> 18551895

Tissue levels of arsenicals and skin tumor response following administration of monomethylarsonous acid and arsenite to K6/ODC mice.

Yan Chen1, Tom O'Brien, Luz Maria Del Razo, David J Thomas, Kirk T Kitchin.   

Abstract

The effects of monomethylarsonous acid (MMA[III]) and arsenite, administered in drinking water on tissue levels of arsenicals, cytogenetics, and mouse skin tumorigenicity were determined. A low-methionine diet modified the pattern of arsenical tissue concentrations and decreased the tissue arsenical concentrations, particularly in kidney and urinary bladder, less so in liver, and had little effect in the lungs. In mice given 75 ppm arsenite and a low-methionine diet, the urinary bladder tissue levels were only 29%, 26%, and 38% of the inorganic arsenic (iAs), MMA, and dimethylarsinic acid (DMA) concentrations found in mice eating the control diet. In K6/ODC transgenic mice that consumed a normal diet (Purina 5002), a 26-week drinking water exposure to 10 ppm arsenite resulted in 5% of the treated animals having squamous skin tumors. Exposure to 10, 50, 75, or 150 ppm MMA(III) caused 5%, 6.7%, 5%, or 0% tumor-bearing animals. A low-methionine diet did not markedly change the incidence of skin tumors--10 ppm arsenite led to 10% tumors. With a low-methionine diet, 10 and 50 ppm, MMA(III) caused 5% and 6.7% tumor-bearing animals. In comparing the frequency of tumors in the concurrent control groups (1/70, 1.4%) with the frequency of tumors in the pooled arsenical-treated responsive groups (8/122, 6.6%), there is an excess of 6 mouse skin tumors observed in the pooled arsenical-responsive treatment groups compared to the expected number of tumors based on frequency of tumors observed in concurrent control mice. In summary, studies with MMA(III) and arsenite-treated K6/ODC transgenic mice showed (1) a low-methionine diet substantially altered mouse tissue arsenical levels and (2) numerically elevated incidence of mouse skin tumors following arsenical exposures.

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Year:  2008        PMID: 18551895     DOI: 10.1615/jenvironpatholtoxicoloncol.v27.i1.50

Source DB:  PubMed          Journal:  J Environ Pathol Toxicol Oncol        ISSN: 0731-8898            Impact factor:   3.567


  5 in total

1.  Cardiac epithelial-mesenchymal transition is blocked by monomethylarsonous acid (III).

Authors:  Tianfang Huang; Joey V Barnett; Todd D Camenisch
Journal:  Toxicol Sci       Date:  2014-08-21       Impact factor: 4.849

2.  Tumors and proliferative lesions in adult offspring after maternal exposure to methylarsonous acid during gestation in CD1 mice.

Authors:  Erik J Tokar; Bhalchandra A Diwan; David J Thomas; Michael P Waalkes
Journal:  Arch Toxicol       Date:  2012-03-08       Impact factor: 5.153

3.  Protective Role of Spermidine in Colitis and Colon Carcinogenesis.

Authors:  Alain P Gobert; Yvonne L Latour; Mohammad Asim; Daniel P Barry; Margaret M Allaman; Jordan L Finley; Thaddeus M Smith; Kara M McNamara; Kshipra Singh; Johanna C Sierra; Alberto G Delgado; Paula B Luis; Claus Schneider; M Kay Washington; M Blanca Piazuelo; Shilin Zhao; Lori A Coburn; Keith T Wilson
Journal:  Gastroenterology       Date:  2021-11-10       Impact factor: 22.682

4.  Joint effects of genomic markers and urinary methylation capacity associated with inorganic arsenic metabolism on the occurrence of cancers among residents in arseniasis-endemic areas: A cohort subset with average fifteen-year follow-up.

Authors:  Pei-Ju Liao; Kuang-Hung Hsu; Hung-Yi Chiou; Chien-Jen Chen; Chih-Hung Lee
Journal:  Biomed J       Date:  2020-10-13       Impact factor: 7.892

5.  Pharmacokinetic and Genomic Effects of Arsenite in Drinking Water on Mouse Lung in a 30-Day Exposure.

Authors:  Jaya Chilakapati; Kathleen Wallace; Araceli Hernandez-Zavala; Tanya Moore; Hongzu Ren; Kirk T Kitchin
Journal:  Dose Response       Date:  2015-06-30       Impact factor: 2.658

  5 in total

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