Literature DB >> 24503412

Species and gender differences in the carcinogenic activity of trimethylolpropane triacrylate in rats and mice.

Inok Surh1, Deepa B Rao2, Mark F Cesta3, Charles D Hébert4, Jill F Mann4, Helen Cunny3, Grace E Kissling3, David Malarkey3, Rajendra S Chhabra3.   

Abstract

Trimethylolpropane triacrylate (TMPTA) is a multifunctional monomer with industrial applications. To determine the carcinogenic potential, male and female F344/N rats and B6C3F1/N mice were administered TMPTA (0, 0.3, 1.0, or 3.0mg/kg) in acetone dermally for 2 years. There were no differences in the body weights and survival in the treated animals compared to controls. Nonneoplastic skin lesions at the site of application included epidermal hyperplasia and hyperkeratosis in both rats and mice. There were no incidences of tumors at the site of application in rats and mice. Rare malignant liver neoplasms were observed in female mice that included hepatoblastoma in the 0.3 and 3.0mg/kg groups, and hepatocholangiocarcinoma in the 1.0 and 3.0mg/kg groups. The incidences of uterine stromal polyp and stromal polyp or stromal sarcoma (combined) in female mice occurred with positive trends and the incidences were significantly increased in the 3.0mg/kg group. A marginal increase in the incidences of malignant mesothelioma in male rats may have been related to TMPTA treatment. In conclusion, our studies show that TMPTA is a dermal irritant in both rats and mice of either sex. Increased incidences of tumor formation were observed in female mice and male rats. Published by Elsevier Ltd.

Entities:  

Keywords:  Carcinogenicity; Liver; Skin; Trimethylolpropane triacrylate; Uterine

Mesh:

Substances:

Year:  2014        PMID: 24503412      PMCID: PMC3995139          DOI: 10.1016/j.fct.2014.01.048

Source DB:  PubMed          Journal:  Food Chem Toxicol        ISSN: 0278-6915            Impact factor:   6.023


  36 in total

1.  Root graviresponsiveness and cellular differentiation in wild-type and a starchless mutant of Arabidopsis thaliana.

Authors:  R Moore
Journal:  Ann Bot       Date:  1989       Impact factor: 4.357

2.  Topical application of representative multifunctional acrylates produced proliferative and inflammatory lesions in F344/N rats and B6C3F1 mice, and squamous cell neoplasms in Tg.AC mice.

Authors:  Adriana M Doi; James R Hailey; Milton Hejtmancik; John D Toft; Molly Vallant; Rajendra S Chhabra
Journal:  Toxicol Pathol       Date:  2005       Impact factor: 1.902

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4.  v-Ha-ras transgene abrogates the initiation step in mouse skin tumorigenesis: effects of phorbol esters and retinoic acid.

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Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

5.  Responses of transgenic mouse lines p53(+/-) and Tg.AC to agents tested in conventional carcinogenicity bioassays.

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Journal:  Toxicol Sci       Date:  2000-02       Impact factor: 4.849

Review 6.  Inflammation: gearing the journey to cancer.

Authors:  Joydeb Kumar Kundu; Young-Joon Surh
Journal:  Mutat Res       Date:  2008-03-16       Impact factor: 2.433

7.  Allergic contact dermatitis due to urethane acrylate in ultraviolet cured inks.

Authors:  J R Nethercott; H R Jakubovic; C Pilger; J W Smith
Journal:  Br J Ind Med       Date:  1983-08

8.  Contact sensitivity to acrylate compounds in guinea pigs.

Authors:  D Parker; J L Turk
Journal:  Contact Dermatitis       Date:  1983-01       Impact factor: 6.600

9.  The sensitizing capacity of multifunctional acrylates in the guinea pig.

Authors:  B Björkner
Journal:  Contact Dermatitis       Date:  1984-10       Impact factor: 6.600

10.  Airborne occupational allergic contact dermatitis due to trimethylolpropane triacrylate (TMPTA) used in the manufacture of printed circuit boards.

Authors:  L Kanerva; K Tarvainen; R Jolanki; M L Henriks-Eckerman; T Estlander
Journal:  Contact Dermatitis       Date:  1998-05       Impact factor: 6.600

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