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Aromatase in normal and diseased liver.

Authors :
Murakami, Keigo
Hata, Shuko
Miki, Yasuhiro
Sasano, Hironobu
Source :
Hormone Molecular Biology & Clinical Investigation. Mar2020, Vol. 41 Issue 1, p1-11. 11p. 2 Color Photographs, 1 Black and White Photograph, 1 Diagram, 3 Charts.
Publication Year :
2020

Abstract

Background: A potential correlation between sex hormones, such as androgens and estrogens, and the development and progression of hepatocellular carcinoma (HCC) has been proposed. However, its details, in particular, aromatase status in diseased human liver has remained largely unknown. Materials and methods: We immunolocalized aromatase, 17β-hydroxysteroid dehydrogenase (17β-HSD) type 1 and 17β-HSD type 2 in a total of 155 cases, consisting of normal liver (n = 10), nonalcoholic steatohepatitis (NASH) (n = 18), primary sclerosing cholangitis (PSC) (n = 6), primary biliary cholangitis (PBC) (n = 13), biliary atresia (n = 18), alcoholic hepatitis (n = 11), hepatitis C virus (HCV) (n = 31), HCV sustained virologic response (HCV-SVR) (n = 10), hepatitis B virus (HBV) (n = 20), HBV sustained virologic response (HBV-SVR) (n = 8) and infants (n = 10). Results: Immunoreactivity scores of aromatase in HBV (59.5 ± 30.9), HBV-SVR (68.1 ± 33.5) and infants (100.5 ± 36.6) were significantly higher than those in normal liver (26.0 ± 17.1). Scores of 17β-HSD type 1 in any etiology other than HBV (116.3 ± 23.7) and infants (120.0 ± 28.5) were significantly lower than those in normal liver (122.5 ± 8.6). Scores of 17β-HSD type 2 in NASH (74.4 ± 36.6) were significantly lower than those in normal liver (128.0 ± 29.7). Conclusion: High immunoreactivity scores of aromatase and 17β-HSD type 1 in the patients with HBV suggest a correlation between HBV infection and in situ estrogen synthesis in hepatocytes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18681883
Volume :
41
Issue :
1
Database :
Academic Search Index
Journal :
Hormone Molecular Biology & Clinical Investigation
Publication Type :
Academic Journal
Accession number :
143023405
Full Text :
https://doi.org/10.1515/hmbci-2017-0081