Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. May 15, 2004; 10(10): 1462-1465
Published online May 15, 2004. doi: 10.3748/wjg.v10.i10.1462
Establishment and characterization of human hepatocellular carcinoma cell line FHCC-98
Chao-Yang Lou, Ying-Ming Feng, Ai-Rong Qian, Yu Li, Hao Tang, Peng Shang, Zhi-Nan Chen
Chao-Yang Lou, Ying-Ming Feng, Department of Oncology, Tangdu Hospital, Fourth Military Medical University, Xi’an 710038, Shaanxi Province, China
Peng Shang, Ai-Rong Qian, Yu Li, Hao Tang, Zhi-Nan Chen, Department of Cell Biology, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China
Author contributions: All authors contributed equally to the work.
Supported by the National High-Tech Research and Development Program of China, NO. 2001AA215061
Correspondence to: Dr. Peng Shang, Department of Cell Biology, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China. chcerc7@fmmu.edu.cn
Telephone: +86-29-83374547
Received: March 15, 2004
Revised: April 2, 2004
Accepted: April 10, 2004
Published online: May 15, 2004
Abstract

AIM: To establish a novel human hepatocellular carcinoma (HCC) cell line FHCC-98 from HCC tissue and to provide a suitable model for studying HCC occurrence, progress and metastasis.

METHODS: Serially passaged cells were cultured and their morphologies were observed under light and electron microscope. Cytogenetic study was conducted by using flow cytometry and chromosome analysis. Expressions of tumor markers such as α-fetoprotein (AFP), cytokeratin (CK) and hepatoma metastasis-associated factor HAb18G/CD147 on the FHCC-98 cells were detected by immunocytochemistry or Western blotting. Lactic dehydrogenase (LDH) isoenzymes were detected by polyacrylamide gel electrophoresis (PAGE). Xenograft was performed by inoculating FHCC-98 cells into the flanks of nude mice.

RESULTS: Morphology of FHCC-98 cells was the same as that of other malignant cells. The expressions of the cells were positive for HAb18G/CD147 and CK, and negative for AFP. Its population doubling time was 21.4 h. The cell DNA was tetraploid and the major chromosomes were triploid by cytogenetics analysis. The tumorigenicity in nude mice was 100%. PAGE showed four bands representing LDH2, LDH3, LDH4 and LDH5.

CONCLUSION: FHCC-98 is a novel HCC cell line and an ideal cell model for further exploring the mechanism of hepatocellular carcinoma invasion and metastasis.

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