Literature DB >> 18456281

Mouse model of diethylnitrosamine-induced gastric cancer.

Marcelo Binato1, Marcelo Kruel Schmidt, Bernardo Silveira Volkweis, Guilherme Behrend Silva Ribeiro, Maria Isabel Edelweiss, Richard Ricachenevsky Gurski.   

Abstract

BACKGROUND: Nitrosamines are associated with the potential to induce cancer in the digestive tract. Ethanol has also been shown to enhance the effects of nitrosamine-induced carcinogenesis. The aim of this study was to investigate a murine model of the prevalence and types of epithelial lesions induced in the stomach by diethylnitrosamine (DEN), and to evaluate the influence of ethanol and N'-nitrosonornicotine (NNN) as promoters of gastric carcinogenesis.
MATERIALS AND METHODS: Two hundred eight (n = 208) mice were distributed into five groups and administered either water (G1), DEN+water (G2), DEN+NNN (G3), DEN+Ethanol (G4), or DEN+NNN+Ethanol (G5) for a period of 180 days. Mice were sacrificed; their stomachs were sectioned and stained with hematoxylin/eosin. Stomachs were analyzed for normal histology; foveolar hyperplasia; gastritis; ulcer; adenoma; metaplasia; dysplasia; squamous-cell cancer (SCC); and adenocarcinoma (ACA).
RESULTS: One hundred eighty-four (N = 184) specimens were studied. No statistically significant differences were observed between the average DEN consumption of groups (P > 0.05). Unlike G1, in all four groups exposed to carcinogens, gastric SCC and ACA were induced (P < 0.001). SCC was identified in 91 (49.5%) and ACA in 77 (41.8%) of all mice (including controls). In 47 mice (25.5%), we identified two histological types of carcinoma that occurred simultaneously. The prevalence of ACA in G5 was higher when compared with the other exposed groups (P < 0.001).
CONCLUSIONS: We created an optimal murine model for investigation of the development of gastric carcinogenesis, as there was a high rate of development of tumors, but low mortality and morbidity. The coadministration of DEN, ethanol, and NNN induced carcinogenesis to the largest extent compared with the other combinations.

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Year:  2008        PMID: 18456281     DOI: 10.1016/j.jss.2007.12.748

Source DB:  PubMed          Journal:  J Surg Res        ISSN: 0022-4804            Impact factor:   2.192


  9 in total

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7.  Liver Protective Effects of Renin-Angiotensin System Inhibition Have No Survival Benefits in Hepatocellular Carcinoma Induced By Repetitive Administration of Diethylnitrosamine in Mice.

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Journal:  Open Access Maced J Med Sci       Date:  2018-06-06

8.  The Carcinogenic Agent Diethylnitrosamine Induces Early Oxidative Stress, Inflammation and Proliferation in Rat Liver, Stomach and Colon: Protective Effect of Ginger Extract.

Authors:  Dina F Mansour; Heba M I Abdallah; Bassant M M Ibrahim; Rehab R Hegazy; Reham S E Esmail; Lubna O Abdel-Salam
Journal:  Asian Pac J Cancer Prev       Date:  2019-08-01

Review 9.  Animal Models of Hepatocellular Carcinoma Prevention.

Authors:  Ram C Shankaraiah; Laura Gramantieri; Francesca Fornari; Silvia Sabbioni; Elisa Callegari; Massimo Negrini
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  9 in total

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