Literature DB >> 7104991

Morphological classification of mouse liver tumors based on biological characteristics.

F F Becker.   

Abstract

Examination of three strains of inbred mice suggested that specific morphological types of hepatic tumors are the result of genetic predisposition while other types of tumors are associated with exposure to chemical carcinogens. A simple classification system is proposed. Additional studies indicated that a putative promoting agent, such as phenobarbital, increased the incidence of those tumor types usually associated with spontaneous appearance and only in strains with a genetic predisposition to spontaneous tumorigenesis. Carcinogens induce an increase in all types of tumors.

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Year:  1982        PMID: 7104991

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  21 in total

1.  Enhancement of chemical hepatocarcinogenesis by the HIV-1 tat gene.

Authors:  G Altavilla; A Caputo; M Lanfredi; C Piola; G Barbanti-Brodano; A Corallini
Journal:  Am J Pathol       Date:  2000-10       Impact factor: 4.307

2.  Phenobarbital does not reduce the concentration of thyroid hormone in CC57BR mice in which it does not promote liver tumor development.

Authors:  V I Kaledin; T A Obut
Journal:  Dokl Biol Sci       Date:  2003 Nov-Dec

Review 3.  Human relevance of rodent liver tumour formation by constitutive androstane receptor (CAR) activators.

Authors:  Brian G Lake
Journal:  Toxicol Res (Camb)       Date:  2018-03-12       Impact factor: 3.524

4.  Characterization of liver injury, oval cell proliferation and cholangiocarcinogenesis in glutathione S-transferase A3 knockout mice.

Authors:  Dana R Crawford; Zoran Ilic; Ian Guest; Ginger L Milne; John D Hayes; Stewart Sell
Journal:  Carcinogenesis       Date:  2017-07-01       Impact factor: 4.944

5.  Differential susceptibility to hepatic inflammation and proliferation in AXB recombinant inbred mice chronically infected with Helicobacter hepaticus.

Authors:  M Ihrig; M D Schrenzel; J G Fox
Journal:  Am J Pathol       Date:  1999-08       Impact factor: 4.307

6.  Multiple genes exhibit phenobarbital-induced constitutive active/androstane receptor-mediated DNA methylation changes during liver tumorigenesis and in liver tumors.

Authors:  Jennifer M Phillips; Jay I Goodman
Journal:  Toxicol Sci       Date:  2009-02-20       Impact factor: 4.849

7.  Phenobarbital elicits unique, early changes in the expression of hepatic genes that affect critical pathways in tumor-prone B6C3F1 mice.

Authors:  Jennifer M Phillips; Lyle D Burgoon; Jay I Goodman
Journal:  Toxicol Sci       Date:  2009-03-06       Impact factor: 4.849

8.  Carcinogenicity study in mice on pildralazine, a hydralazinelike antihypertensive compound.

Authors:  G Della Porta; T A Dragani
Journal:  J Cancer Res Clin Oncol       Date:  1983       Impact factor: 4.553

9.  Genetic susceptibility to murine hepatocarcinogenesis is associated with high growth rate of NDEA-initiated hepatocytes.

Authors:  T A Dragani; G Manenti; G Della Porta
Journal:  J Cancer Res Clin Oncol       Date:  1987       Impact factor: 4.553

10.  The constitutive active/androstane receptor facilitates unique phenobarbital-induced expression changes of genes involved in key pathways in precancerous liver and liver tumors.

Authors:  Jennifer M Phillips; Lyle D Burgoon; Jay I Goodman
Journal:  Toxicol Sci       Date:  2009-05-29       Impact factor: 4.849

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