Literature DB >> 6825204

Phenobarbital as a promoter in the initiation/selection process of experimental rat hepatocarcinogenesis.

M Lans, J de Gerlache, H S Taper, V Préat, M B Roberfroid.   

Abstract

Supplementary introduction of a phenobarbital (PB) promotion step after the Solt and Farber procedure dramatically increases the number of phenotypically-altered hepatocytes. These hepatocytes occupy approximately 40% of the liver volume after one week of PB treatment. These areas constitute a relatively uniform cellular population with altered histological phenotype and with distinct histochemical markers used by other authors for the detection of premalignancy. This procedure leads to the appearance of numerous hepatocellular carcinomas at approximately the 36 weeks stage. It was suggested that the early hepatocellular alterations after the initiation/selection procedure followed by PB might correspond to the hyperplasia of phenotypically-altered epidermal cells at the conversion step of mouse skin tumor promotion.

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Year:  1983        PMID: 6825204     DOI: 10.1093/carcin/4.2.141

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  8 in total

1.  Macrolide antibiotics differentially influence human HepG2 cytotoxicity and modulate intrinsic/extrinsic apoptotic pathways in rat hepatocellular carcinoma model.

Authors:  Nagwa I Abdel-Hamid; Mona F El-Azab; Yasser M Moustafa
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2017-01-09       Impact factor: 3.000

Review 2.  Models of carcinogenesis: an overview.

Authors:  Paolo Vineis; Arthur Schatzkin; John D Potter
Journal:  Carcinogenesis       Date:  2010-04-29       Impact factor: 4.944

Review 3.  Tumor promotion in the liver.

Authors:  R Schulte-Hermann
Journal:  Arch Toxicol       Date:  1985-08       Impact factor: 5.153

4.  Increased silver stainability of metaphase chromosomes from rat hepatocytes during in vivo hepatocarcinogenesis.

Authors:  M Kirsch-Volders; A Deleener; M Lans; J de Gerlache
Journal:  Experientia       Date:  1985-09-15

5.  Oncological outcomes in rats given nephrocarcinogenic exposure to dietary ochratoxin a, followed by the tumour promoter sodium barbital for life: a pilot study.

Authors:  Peter G Mantle; Miloslav Dobrota; Cheryl E Gillett; Edward W Odell; Sarah E Pinder
Journal:  Toxins (Basel)       Date:  2010-03-31       Impact factor: 4.546

6.  Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat.

Authors:  P Castelain; A Deleener; M Kirsch-Volders; H Barbason
Journal:  Br J Cancer       Date:  1989-12       Impact factor: 7.640

Review 7.  Multiple end point procedure to evaluate risk from pesticides.

Authors:  G Cantelli-Forti; M Paolini; P Hrelia
Journal:  Environ Health Perspect       Date:  1993-10       Impact factor: 9.031

8.  Inhibitory effects of inhibitors of arachidonic acid metabolism on the evolution of rat liver preneoplastic foci into nodules and hepatocellular carcinomas with or without phenobarbital exposure.

Authors:  Q Tang; A Denda; T Tsujiuchi; M Tsutsumi; T Amanuma; Y Murata; H Maruyama; Y Konishi
Journal:  Jpn J Cancer Res       Date:  1993-02
  8 in total

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