Literature DB >> 10027411

Oval cell numbers in human chronic liver diseases are directly related to disease severity.

K N Lowes1, B A Brennan, G C Yeoh, J K Olynyk.   

Abstract

The risk of developing hepatocellular carcinoma is significantly increased in patients with genetic hemochromatosis, alcoholic liver disease, or chronic hepatitis C infection. The precise mechanisms underlying the development of hepatocellular carcinoma in these conditions are not well understood. Stem cells within the liver, termed oval cells, are involved in the pathogenesis of hepatocellular carcinoma in animal models and may be important in the development of hepatocellular carcinoma in human chronic liver diseases. The aims of this study were to determine whether oval cells could be detected in the liver of patients with genetic hemochromatosis, alcoholic liver disease, or chronic hepatitis C, and whether there is a relationship between the severity of the liver disease and the number of oval cells. Oval cells were detected using histology and immunohistochemistry in liver biopsies from patients with genetic hemochromatosis, alcoholic liver disease, or chronic hepatitis C. Oval cells were not observed in normal liver controls. Oval cell numbers increased significantly with the progression of disease severity from mild to severe in each of the diseases studied. We conclude that oval cells are frequently found in subjects with genetic hemochromatosis, alcoholic liver disease, or chronic hepatitis C. There is an association between severity of liver disease and increase in the number of oval cells consistent with the hypothesis that oval cell proliferation is associated with increased risk for development of hepatocellular carcinoma in chronic liver disease.

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Year:  1999        PMID: 10027411      PMCID: PMC1849988          DOI: 10.1016/S0002-9440(10)65299-6

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  18 in total

1.  Expression of alpha, mu and pi class glutathione S-transferases in oval and ductal cells in liver of rats placed on a choline-deficient, ethionine-supplemented diet.

Authors:  L B Tee; P G Smith; G C Yeoh
Journal:  Carcinogenesis       Date:  1992-10       Impact factor: 4.944

2.  Bile duct changes in alcoholic liver disease. The Veterans Administration Cooperative Study Group.

Authors:  M B Ray; C L Mendenhall; S W French; P S Gartside
Journal:  Liver       Date:  1993-02

3.  Gadolinium chloride suppresses hepatic oval cell proliferation in rats with biliary obstruction.

Authors:  J K Olynyk; G C Yeoh; G A Ramm; S L Clarke; P M Hall; R S Britton; B R Bacon; T F Tracy
Journal:  Am J Pathol       Date:  1998-02       Impact factor: 4.307

4.  Prevalence of antibodies to hepatitis C virus in Italian patients with hepatocellular carcinoma.

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Journal:  Lancet       Date:  1989-10-28       Impact factor: 79.321

Review 5.  Evidence for the stem cell origin of hepatocellular carcinoma and cholangiocarcinoma.

Authors:  S Sell; H A Dunsford
Journal:  Am J Pathol       Date:  1989-06       Impact factor: 4.307

6.  Oval cell proliferation and the origin of small hepatocytes in liver injury induced by D-galactosamine.

Authors:  J M Lemire; N Shiojiri; N Fausto
Journal:  Am J Pathol       Date:  1991-09       Impact factor: 4.307

7.  Hepatic cirrhosis: a clinico-pathological review of 520 cases.

Authors:  R N MacSween; A R Scott
Journal:  J Clin Pathol       Date:  1973-12       Impact factor: 3.411

8.  Risk factors for hepatocellular carcinoma among patients with chronic liver disease.

Authors:  H Tsukuma; T Hiyama; S Tanaka; M Nakao; T Yabuuchi; T Kitamura; K Nakanishi; I Fujimoto; A Inoue; H Yamazaki
Journal:  N Engl J Med       Date:  1993-06-24       Impact factor: 91.245

9.  A precursor-product relationship exists between oval cells and hepatocytes in rat liver.

Authors:  R P Evarts; P Nagy; E Marsden; S S Thorgeirsson
Journal:  Carcinogenesis       Date:  1987-11       Impact factor: 4.944

10.  Occurrence of oval-type cells in hepatitis B virus-associated human hepatocarcinogenesis.

Authors:  C C Hsia; R P Evarts; H Nakatsukasa; E R Marsden; S S Thorgeirsson
Journal:  Hepatology       Date:  1992-12       Impact factor: 17.425

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  147 in total

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4.  Centrilobular ductular reaction correlates with fibrosis stage and fibrosis progression in non-alcoholic steatohepatitis.

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5.  The vagal nerve stimulates activation of the hepatic progenitor cell compartment via muscarinic acetylcholine receptor type 3.

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Journal:  Am J Pathol       Date:  2002-08       Impact factor: 4.307

Review 6.  Viral hepatitis: new data on hepatitis C infection.

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Journal:  Pathol Oncol Res       Date:  2003-12-22       Impact factor: 3.201

7.  Possible stem cell origin of human cholangiocarcinoma.

Authors:  Chao Liu; Jie Wang; Qing-Jia Ou
Journal:  World J Gastroenterol       Date:  2004-11-15       Impact factor: 5.742

8.  FGF7 is a functional niche signal required for stimulation of adult liver progenitor cells that support liver regeneration.

Authors:  Hinako M Takase; Tohru Itoh; Seitaro Ino; Ting Wang; Takehiko Koji; Shizuo Akira; Yasuhiro Takikawa; Atsushi Miyajima
Journal:  Genes Dev       Date:  2013-01-15       Impact factor: 11.361

9.  Expression of stromal cell-derived factor-1 and of its receptor CXCR4 in liver regeneration from oval cells in rat.

Authors:  Philippe Mavier; Nadine Martin; Dominique Couchie; Anne-Marie Préaux; Yannick Laperche; Elie Serge Zafrani
Journal:  Am J Pathol       Date:  2004-12       Impact factor: 4.307

Review 10.  The origin, biology, and therapeutic potential of facultative adult hepatic progenitor cells.

Authors:  Soona Shin; Klaus H Kaestner
Journal:  Curr Top Dev Biol       Date:  2014       Impact factor: 4.897

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