Literature DB >> 6138303

Mallory body formation runs parallel to gamma-glutamyl transferase induction in hepatocytes of griseofulvin-fed mice.

J Tazawa, T Irie, S W French.   

Abstract

To evaluate whether Mallory bodies (MBs) are linked to the induction of the enzyme gamma-glutamyl transferase (GGT), mice were fed 2.5% griseofulvin (GF). The experimental and control mice livers were examined at four time periods, i.e., after 4 months' of GF feeding, 1 month after GF withdrawal and 13 days after GF refeeding, and at sacrifice after 4 months of GF withdrawal. The livers from mice continuously fed GF or control diet for 10 months were also examined. Tumors and nontumorous livers were examined histologically, histochemically, electron microscopically, and immunocytochemically. The tumors consisted of hepatomas and hyperplastic nodules. To localize MBs inside GGT-positive cells, a double-staining method was employed; GGT-positive cells were identified histochemically followed by staining for MBs using the unlabeled immunoperoxidase technique. The per cent area of the GGT-positive foci was closely correlated with the frequency of MBs observed in the course of a GF feeding and withdrawal. Almost all of the MBs were located in GGT-positive cells in both tumors and nontumor liver tissue. MBs and GGT positivity involved the same liver cells. They both were found in high frequency in tumors induced by GF. These results indicate that MB formation, like GGT induction, is a phenotypic change induced by GF. The coexistence of the two phenomenon in the same cell throughout all phases of tumor formation suggests that MBs may be related to the neoplastic process in the GF-fed mouse model.

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Year:  1983        PMID: 6138303     DOI: 10.1002/hep.1840030617

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  10 in total

1.  Mallory body formation is associated with epigenetic phenotypic change in hepatocytes in vivo.

Authors:  Fawzia Bardag-Gorce; Jennifer Dedes; Barbara A French; Joan V Oliva; Jun Li; Samuel W French
Journal:  Exp Mol Pathol       Date:  2007-03-30       Impact factor: 3.362

2.  Cytophotometric DNA analysis of hepatocellular carcinoma with Mallory bodies.

Authors:  M Hoso; Y Nakanuma
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1989

3.  Keratin 8 phosphorylation regulates its transamidation and hepatocyte Mallory-Denk body formation.

Authors:  Raymond Kwan; Shinichiro Hanada; Masaru Harada; Pavel Strnad; Daniel H Li; M Bishr Omary
Journal:  FASEB J       Date:  2012-02-23       Impact factor: 5.191

4.  Alcoholic liver disease - Hepatocellular carcinoma transformation.

Authors:  Samuel W French; James Lee; Jim Zhong; Timothy R Morgan; Virgil Buslon; William Lungo; Barbara A French
Journal:  J Gastrointest Oncol       Date:  2012-09

5.  The Japanese Society of Gastroenterology. Proceedings of the 72nd general meeting. Niigata, Japan, March 27-29, 1986. Abstracts.

Authors: 
Journal:  Gastroenterol Jpn       Date:  1986-12

Review 6.  The role of innate immunity in the pathogenesis of preneoplasia in drug-induced chronic hepatitis based on a mouse model.

Authors:  S W French; F Bardag-Gorce; B A French; J Li; J Oliva
Journal:  Exp Mol Pathol       Date:  2011-07-28       Impact factor: 3.362

7.  Fat10 is an epigenetic marker for liver preneoplasia in a drug-primed mouse model of tumorigenesis.

Authors:  Joan Oliva; Fawzia Bardag-Gorce; Barbara A French; Jun Li; Laron McPhaul; Fataneh Amidi; Jeniffer Dedes; Amir Habibi; Sheila Nguyen; Samuel W French
Journal:  Exp Mol Pathol       Date:  2008-01-11       Impact factor: 3.362

8.  Balloon liver cells forming Mallory-Denk-bodies are progenitor cells.

Authors:  S W French; E Vitocruz; B A French
Journal:  Exp Mol Pathol       Date:  2013-06-14       Impact factor: 3.362

Review 9.  Molecular events in hepatic preneoplasia: a review.

Authors:  S W French
Journal:  Exp Mol Pathol       Date:  2010-01-22       Impact factor: 3.362

10.  S-adenosylmethionine prevents Mallory Denk body formation in drug-primed mice by inhibiting the epigenetic memory.

Authors:  Jun Li; Fawzia Bardag-Gorce; Jennifer Dedes; Barbara Alan French; Fataneh Amidi; Joan Oliva; Samuel William French
Journal:  Hepatology       Date:  2008-02       Impact factor: 17.425

  10 in total

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