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Citations to this article

Bile acid synthesis by long-term cultured cell line established from human hepatoblastoma.
Y Amuro, … , H Nakabayashi, J Sato
Y Amuro, … , H Nakabayashi, J Sato
Published November 1, 1982
Citation Information: J Clin Invest. 1982;70(5):1128-1130. https://doi.org/10.1172/JCI110701.
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Research Article

Bile acid synthesis by long-term cultured cell line established from human hepatoblastoma.

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Abstract

Bile acids in the spent medium for the cell culture were analyzed by gas-liquid chromatography and gas-liquid chromatography-mass spectrometry to determine whether human hepatoblastoma cell line could synthesize bile acids. Cholic, chenodeoxycholic, and lithocolic acids were found in the culture medium, and a portion of chenodeoxycholic acid and all of lithocholic acid were sulfated. Since the cells had been cultured in serum-free medium, it is clear that the bile acids were newly synthesized and sulfated by the cultured cells. Chenodeoxycholic acid was the main bile acid in the medium, suggesting that the cell line might predominantly synthesize chenodeoxycholic acid. On the other hand, the cells had fetal or hepatoma characters such as marked alpha-fetoprotein production. These results suggest that fetal or hepatoma type bile acid metabolism might occur in the cell line, and that the established cell line could be an useful in vitro model for the study of bile acid metabolism in hepatoma.

Authors

Y Amuro, M Tanaka, K Higashino, E Hayashi, T Endo, S Kishimoto, H Nakabayashi, J Sato

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Total citations by year

Year: 2001 1994 1993 1987 1986 1985 1983 Total
Citations: 1 1 1 3 3 1 2 12
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article (12)

Title and authors Publication Year
Predominance of human versus rat phenotype in the metabolic pathways for bile acid synthesis by hybrid WIF-B9 cells
MJ Monte, MD Badia, MA Serrano, MP Sacristan, D Cassio, JJ Marin
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 2001
Atlas of Human Tumor Cell Lines
YC Hung, PG Satyaswaroop, S Tabibzadeh
Atlas of Human Tumor Cell Lines 1994
Human hepatoblastoma cells (HepG2) and rat hepatoma cells are defective in important enzyme activities in the oxidation of the C27 steroid side chain in bile acid formation
AK Farrants, A Nilsson, JI Pedersen
Journal of lipid research 1993
Bile acid composition in primary hepatocellular carcinoma
F Nakayama, J Yanagisawa, H Miyazaki, M Itoh
Journal of Gastroenterology and Hepatology 1987
Cholesterol metabolism and sterol carrier protein-2 (non-specific lipid transfer protein)
MJ Geelen, AC Beynen, KW Wirtz
International Journal of Biochemistry 1987
Neoplasms of the Liver
K Okuda, KG Ishak
1987
Fecal bile acids and neutral sterols in rats with spontaneous colon cancer
E Hayashi, Y Amuro, T Endo, H Yamamoto, M Miyamoto, S Kishimoto
International Journal of Cancer 1986
HepG2. A human hepatoblastoma cell line exhibiting defects in bile acid synthesis and conjugation
GT Everson, MA Polokoff
The Journal of biological chemistry 1986
Hepatocyte-hepatoma cell hybrids. Characterization and demonstration of bile acid synthesis
MA Polokoff, GT Everson
The Journal of biological chemistry 1986
Reduction of 3-keto-5β-cholanoic acid to lithocholic and isolithocholic acids by human liver cytosol in vitro
A Yoshiki, Y Wataru, M Akio, H Toshikazu, H Kazuya
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism 1985
Stimulation of bile acid synthesis by dibutyryl cyclic AMP in isolated rat hepatocytes
GS Sundaram, V Rothman, S Margolis
Lipids 1983
Production of fibronectin by HUH6 Cl5 cell line established from a human hepatoblastoma
M Tanaka, K Kawamura, M Fang, K Higashino, S Kishimoto, H Nakabayashi, J Sato
Biochemical and Biophysical Research Communications 1983

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