» Articles » PMID: 28152020

Highly Tumorigenic Hepatocellular Carcinoma Cell Line with Cancer Stem Cell-like Properties

Overview
Journal PLoS One
Date 2017 Feb 3
PMID 28152020
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

There are limited numbers of models to study hepatocellular carcinoma (HCC) in vivo in immunocompetent hosts. In an effort to develop a cell line with improved tumorigenicity, we derived a new cell line from Hepa1-6 cells through an in vivo passage in C57BL/6 mice. The resulting Dt81Hepa1-6 cell line showed enhanced tumorigenicity compared to Hepa1-6 with more frequent (28±12 vs. 0±0 lesions at 21 days) and more rapid tumor development (21 (100%) vs. 70 days (10%)) in C57BL/6 mice. The minimal Dt81Hepa1-6 cell number required to obtain visible tumors was 100,000 cells. The Dt81Hepa1-6 cell line showed high hepatotropism with subcutaneous injection leading to liver tumors without development of tumors in lungs or spleen. In vitro, Dt81Hepa1-6 cells showed increased anchorage-independent growth (34.7±6.8 vs. 12.3±3.3 colonies; P<0.05) and increased EpCAM (8.7±1.1 folds; P<0.01) and β-catenin (5.4±1.0 folds; P<0.01) expression. A significant proportion of Dt81Hepa1-6 cells expressed EpCAM compared to Hepa1-6 (34.8±1.1% vs 0.9±0.13%; P<0.001). Enriched EpCAM+ Dt81Hepa1-6 cells led to higher tumor load than EpCAM- Dt81Hepa1-6 cells (1093±74 vs 473±100 tumors; P<0.01). The in vivo selected Dt81Hepa1-6 cell line shows high liver specificity and increased tumorigenicity compared to Hepa1-6 cells. These properties are associated with increased expression of EpCAM and β-catenin confirming that EpCAM+ HCC cells comprise a subset with characteristics of tumor-initiating cells with stem/progenitor cell features. The Dt81Hepa1-6 cell line with its cancer stem cell-like properties will be a useful tool for the study of hepatocellular carcinoma in vivo.

Citing Articles

Invariant NK T cells counteract HCC metastasis by mediating the migration of splenic CD4 T cells into the white pulp and infiltration of B cells.

Geng J, Xie M, Yan M, Xie X, Wang F, Zhu R Commun Biol. 2025; 8(1):351.

PMID: 40033139 PMC: 11876620. DOI: 10.1038/s42003-025-07798-2.


Reprogramming of Glutamine Amino Acid Transporters Expression and Prognostic Significance in Hepatocellular Carcinoma.

Tambay V, Raymond V, Voisin L, Meloche S, Bilodeau M Int J Mol Sci. 2024; 25(14).

PMID: 39062801 PMC: 11277143. DOI: 10.3390/ijms25147558.


Syngeneic mouse model of YES-driven metastatic and proliferative hepatocellular carcinoma.

Voisin L, Lapouge M, Saba-El-Leil M, Gombos M, Javary J, Trinh V Dis Model Mech. 2024; 17(7).

PMID: 39051113 PMC: 11552496. DOI: 10.1242/dmm.050553.


Effects of Dopamine on stem cells and its potential roles in the treatment of inflammatory disorders: a narrative review.

Liu G, Liu Z, Lin Z, Chen P, Yan Y, Lin Q Stem Cell Res Ther. 2023; 14(1):230.

PMID: 37649087 PMC: 10469852. DOI: 10.1186/s13287-023-03454-w.


ENO1 promotes liver carcinogenesis through YAP1-dependent arachidonic acid metabolism.

Sun L, Suo C, Zhang T, Shen S, Gu X, Qiu S Nat Chem Biol. 2023; 19(12):1492-1503.

PMID: 37500770 DOI: 10.1038/s41589-023-01391-6.


References
1.
Schmits R, Filmus J, Gerwin N, Senaldi G, Kiefer F, Kundig T . CD44 regulates hematopoietic progenitor distribution, granuloma formation, and tumorigenicity. Blood. 1997; 90(6):2217-33. View

2.
Chaves-Perez A, Mack B, Maetzel D, Kremling H, Eggert C, Harreus U . EpCAM regulates cell cycle progression via control of cyclin D1 expression. Oncogene. 2012; 32(5):641-50. DOI: 10.1038/onc.2012.75. View

3.
Mamo S, Gal A, Bodo S, Dinnyes A . Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro. BMC Dev Biol. 2007; 7:14. PMC: 1832186. DOI: 10.1186/1471-213X-7-14. View

4.
Munz M, Baeuerle P, Gires O . The emerging role of EpCAM in cancer and stem cell signaling. Cancer Res. 2009; 69(14):5627-9. DOI: 10.1158/0008-5472.CAN-09-0654. View

5.
Yamashita T, Forgues M, Wang W, Kim J, Ye Q, Jia H . EpCAM and alpha-fetoprotein expression defines novel prognostic subtypes of hepatocellular carcinoma. Cancer Res. 2008; 68(5):1451-61. DOI: 10.1158/0008-5472.CAN-07-6013. View