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Authenticated Liver Cancer Cell Lines for Cancer Research

Amongst liver cancers, the incidence of hepatocellular carcinoma (HCC) is increasing and has a high mortality rate. Chronic hepatitis B- or hepatitis C-induced cirrhosis is the leading risk factor for HCC. For reasons that are not entirely known, males may be three to five times more likely than females to develop HCC, the most common type of liver cancer. 83% of cases are diagnosed in less-developed countries, with the highest rates found in east and southeast Asia and in middle and western Africa; rates are lower in south-central and western Asia. The five-year survival rate is 31% for patients who are diagnosed at an early stage, but drops to 3% if cancer has metastasized to other tissues of the body.1

Types of Liver Cancer

Hepatocellular carcinoma accounts for 80% of all adult liver cancers. Cholangiocarcinoma (bile duct cancer) and angiosarcoma comprise 10-20% and 1% of liver cancer diagnoses, respectively.

Type of cancerHepatocellular carcinomaCholangiocarcinomaAngiosarcoma
Tissue of originLiverBile duct tissueHepatic blood
vessels

Risk Factors

The major risk factor for liver cancer is exposure to hepatitis viruses and environmental pathogens. Hepatitis B virus (HBV) infection accounts for 60% of total liver cancer, and hepatitis C virus (HCV) is responsible for 33%. Other risk factors include alcohol-related cirrhosis, nonalcoholic fatty liver disease, and obesity.

Mutations

The most commonly mutated genes in liver cancer are TP53CTNNB1TERTHNF1ALRP1BARID1AAXIN1ARID2KMT2C, and IL6ST.

Click on the genes (above) to find relevant products (antibodies, shRNA, siRNA, primers, CRISPR plasmids) for your research study.

Small Molecules/Monoclonal Antibodies

Small molecule compounds and antibodies can be used to target cancer cells and block tumor growth and progression.  The most common strategy for hepatocellular carcinoma is inhibition of angiogenesis signals.  Drugs used to target liver cancer include:

  • Sorafenib Tosylate (Nexavar)
  • Regorafenib (Stivarga)

Applications

Cancer cell lines are essential for cancer research, and provide an accessible, cost-effective model for cellular behavior and response. Based on cell phenotype and experimental need, cell lines have the potential for utility in multiple applications. Some examples of application-specific cell line use are included below.

ApplicationCell line used
In vitro screeningHepatic cancer cell lines like Huh-7D12  were used to test the cytotoxic effects of plant extracts3 and chemical compounds4
Target identification/validationHepatocellular carcinoma cell lines, including HepG2Hep3B, Huh7, C3A, PLC, LO2, and SUN387 were used to validate the role of p53-miR-1246-NFIB pathway in disease pathogenesis5  
Toxicology studiesSpheroids derived from HepG2 were used for repeated dose high-throughput toxicity studies6
Metastasis studiesSK-HEP-1 cells were used to screen drugs that inhibit metastasis7
Xenograft modelsHepG2 cell lines were used to develop xenograft models of hepatocellular carcinoma8
In-vitro modelsHepG2 cells were modeled to study the life cycle of hepatitis B virus9
Rat hepatocytes (McA RH-7777) and human hepatocytes (HepG2) were used as in vitro models for ischemia/reperfusion diseases10
miRNA regulation studiesNCTC 1469 cell lines were used to study the role of MiR-19a in glycogen synthesis of hepatocytes11

ECACC Liver Cancer Cell Lines

Product No.Cell NameCell Line Origin
87050701ARL-6Rat Wistar liver hepatoma
94101906C2Rat hepatoma [HGPRT-]
94101907C2-Rev 7Rat hepatoma [HGPRT-]
89042701FaoRat hepatoma
87031301H-4-II-ERat hepatoma Reuber H35
85061112H4-II-E-C3Rat liver hepatoma
89102001H4SRat liver hepatoma
94101905H5Rat hepatoma
86062703Hep 3BHuman hepatocyte carcinoma
85011430Hep G2Human Caucasian hepatocyte carcinoma
92110305Hepa 1-6Mouse hepatoma
95090613Hepa-1c1c7Mouse hepatoma
94101908HF1Rat hepatoma Hybrid [H5xFao]
94101909HF1-5Rat hepatoma Hybrid [H5xFao]
93120108HTCRat hepatoma
85061110HTC (BUdR)Rat liver hepatoma
1042712Huh-7D12Human hepatocellular carcinoma
90021504MCA-RH 7777Rat Buffalo hepatoma
96121721MH-22AMouse C3HA hepatocarcinoma
90011902N1-S1Rat hepatoma
91091816SK-HEP-1Human liver adenocarcinoma

References

2.
Liu C, Chen K, Chen P. 2015. Treatment of Liver Cancer. Cold Spring Harb Perspect Med. 5(9):a021535. https://doi.org/10.1101/cshperspect.a021535
3.
Tundis R, Loizzo MR, Menichini F, Bonesi M, Colica C, Menichini F. 2011. In vitro Cytotoxic Activity of Extracts and Isolated Constituents of Salvia leriifoliaBenth. against a Panel of Human Cancer Cell Lines. Chemistry & Biodiversity. 8(6):1152-1162. https://doi.org/10.1002/cbdv.201000311
4.
Bonesi M, Tundis R, Deguin B, Loizzo MR, Menichini F, Tillequin F, Menichini F. 2008. In vitro biological evaluation of novel 7-O-dialkylaminoalkyl cytotoxic pectolinarigenin derivatives against a panel of human cancer cell lines. Bioorganic & Medicinal Chemistry Letters. 18(20):5431-5434. https://doi.org/10.1016/j.bmcl.2008.09.037
5.
ZHANG Q, CAO L, CHENG S, ZHANG A, JIN X, LI Y. 2015. p53-induced microRNA-1246 inhibits the cell growth of human hepatocellular carcinoma cells by targeting NFIB. 33(3):1335-1341. https://doi.org/10.3892/or.2015.3715
6.
Ramaiahgari SC, den Braver MW, Herpers B, Terpstra V, Commandeur JNM, van de Water B, Price LS. A 3D in vitro model of differentiated HepG2 cell spheroids with improved liver-like properties for repeated dose high-throughput toxicity studies. Arch Toxicol. https://doi.org/10.1007/s00204-014-1215-9
7.
Chen H, Yang C, Chen J, Yueh T, Hu M. 2015. Multicarotenoids at Physiological Levels Inhibit Metastasis in Human Hepatocarcinoma SK-Hep-1 Cells. Nutrition and Cancer. 67(4):676-686. https://doi.org/10.1080/01635581.2015.1019633
8.
Liu YM, Xia Y, Dai W, Han HY, Dong YX, Cai J, Zeng X, Luo FY, Yang T, Li YZ, et al. 2014. Cholesterol-conjugated let-7amimics: antitumor efficacy on hepatocellular carcinoma in vitro and in a preclinical orthotopic xenograft model of systemic therapy. BMC Cancer. 14(1): https://doi.org/10.1186/1471-2407-14-889
9.
Sells MA, Chen ML, Acs G. 1987. Production of hepatitis B virus particles in Hep G2 cells transfected with cloned hepatitis B virus DNA.. Proceedings of the National Academy of Sciences. 84(4):1005-1009. https://doi.org/10.1073/pnas.84.4.1005
10.
Hu Q, Wood CR, Cimen S, Venkatachalam AB, Alwayn IPJ. Mitochondrial Damage-Associated Molecular Patterns (MTDs) Are Released during Hepatic Ischemia Reperfusion and Induce Inflammatory Responses. PLoS ONE. 10(10):e0140105. https://doi.org/10.1371/journal.pone.0140105
11.
Dou L, Meng X, Sui X, Wang S, Shen T, Huang X, Guo J, Fang W, Man Y, Xi J, et al. 2015. MiR-19a regulates PTEN expression to mediate glycogen synthesis in hepatocytes. Sci Rep. 5(1): https://doi.org/10.1038/srep11602
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