| Literature DB >> 35470702 |
Jia-Yan Li1, Li-Li Wang1, Jing Fan1, Du-Xian Liu2, Jian-Bo Han3, Yu-Feng Zhang3, Dan-Dan Yin1, Yong-Xiang Yi1,3.
Abstract
Liver cancer (LC) is one of the most common malignant tumors worldwide. Since the mechanism of LC pathogenesis and metastasis cannot be carried out directly on the human body, it is particularly important to establish human liver cancer cell lines for research in vitro. In this study, tissue block adherence method combined with cell clumps digestion method was used to establish primary human hepatocytes (PHHs) with a successful rate of 60% (45/75). Short tandem repeat (STR) analysis proved the cells were derived from its paired tissues. These cells from hepatocellular carcinoma (HCC) expressed NTCP and secreted ALB and AAT as detected by western blot, and expressed hepatocyte-specific membrane protein ASGR1 as detected by flow cytometry. Liver cancer biomarkers like CK7 in ICC (intrahepatic cholangiocarcinoma), AFP, and GPC3 in HCC expressed of different degree as detected by immunohistochemical analysis. These cells displayed typical liver cancer cell morphological characteristics and can passage stably. In conclusion, we developed an effective method to establish PHHs. Further studies are necessary to study if these cells maintaining other liver function and reproduce the physiology of the tumors and how these cells behavior in the drug development.Entities:
Keywords: 2D culture technologies; Liver cell culture; primary human hepatocytes
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Year: 2022 PMID: 35470702 PMCID: PMC9189565 DOI: 10.1177/15353702221085534
Source DB: PubMed Journal: Exp Biol Med (Maywood) ISSN: 1535-3699