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Cell Spheroids with Enhanced Aggressiveness to Mimic Human Liver Cancer In Vitro and In Vivo.
- Source :
-
Scientific reports [Sci Rep] 2017 Sep 05; Vol. 7 (1), pp. 10499. Date of Electronic Publication: 2017 Sep 05. - Publication Year :
- 2017
-
Abstract
- We fabricated a spheroid-forming unit (SFU) for efficient and economic production of cell spheroids. We optimized the protocol for generating large and homogenous liver cancer cell spheroids using Huh7 hepatocellular carcinoma (HCC) cells. The large Huh7 spheroids showed apoptotic and proliferative signals in the centre and at the surface, respectively. In particular, hypoxia-induced factor-1 alpha (HIF-1α) and ERK signal activation were detected in the cell spheroids. To diminish core necrosis and increase the oncogenic character, we co-cultured spheroids with 2% human umbilical vein endothelial cells (HUVECs). HUVECs promoted proliferation and gene expression of HCC-related genes and cancer stem cell markers in the Huh7 spheroidsby activating cytokine signalling, mimicking gene expression in liver cancer. HUVECs induced angiogenesis and vessel maturation in Huh7 spheroids in vivo by activating epithelial-mesenchymal transition and angiogenic pathways. The large Huh7 cell spheroids containing HUVECs survived at higher concentrations of anti-cancer drugs (doxorubicin and sorafenib) than did monolayer cells. Our large cell spheroid provides a useful in vitro HCC model to enable intuitive observation for anti-cancer drug testing.
- Subjects :
- Animals
Carcinoma, Hepatocellular genetics
Carcinoma, Hepatocellular metabolism
Cell Culture Techniques
Cell Line, Tumor
Coculture Techniques
Disease Models, Animal
Gene Expression Profiling
Human Umbilical Vein Endothelial Cells
Humans
Liver Neoplasms genetics
Liver Neoplasms metabolism
Mice
Transcriptome
Tumor Cells, Cultured
Tumor Microenvironment
Xenograft Model Antitumor Assays
Carcinoma, Hepatocellular pathology
Liver Neoplasms pathology
Spheroids, Cellular
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 28874716
- Full Text :
- https://doi.org/10.1038/s41598-017-10828-7