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Survival advantages of multicellular spheroids vs. monolayers of HepG2 cells in vitro
Periodical: Oncology Reports ISBN: 1021-335X
Number: 6
Language: English
Pages: 1465-1471
Authors:Li, C. L., Tian, T., Nan, K. J., Zhao, N., Guo, Y. H., Cui, J., Wang, J., Zhang, W. G.
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Abstract
Mammalian cells grow in three-dimensions (3-D) in vivo. Commonly used two-dimensional (2-D) cell Cultures are inadequate to recreate the biological microenvironment of tumor cells. The potentially different outcomes from 2-D and 3-D culture systems may have a significant impact oil the relevance of experimental findings. The purpose of this study was to characterize the human hepatoma cell line HepG2 in 2-D and 3-D Cultures. HepG2 cells in 2-D and 3-D cultures were treated with cisplatin, 5-fluorouracil, and adriamycin and were analyzed by scanning electron microscopy and transmission electron microscopy. Cell cycle progression and apoptosis were detected by flow cytometry. Inhibition of cell proliferation was quantified by MTT assay. The expression of E-cadherin, CD44v6, VEGF, KDR, endostatin, Bax, and cytochrome-c were analyzed by immunohistochemical (IHC) staining. As compared to the 2-D monolayer culture, the 3-D multicellular spheroids (MCS) of HepG2 cells featured a greater fraction of cells in G I phase and were organized with more abundant cell-cell adhesion. In addition, cells in MCS were significantly less apoptotic in maintenance culture media and were more resistant to drug-induced apoptosis. E-cadherin, CD44v6, VEGF, KDR, endostatin, and cytochrome-c levels were increased in MCS as compared to 2-D cell cultures. In coclusion, MCS conferred differ-entiated phenotypes including increased cell-cell adhesion and G1 phase cell cycle arrest, enhanced cellular resistance to apoptosis, and upregulated angiogenic potential. Based on our data, a multicellular morphological hierarchy may sustain the growth/survival advantages of cancer cells in vivo. Therefore, a 3-D culture system should be the preferred technique for cancer biology investigation.
Mammalian cells grow in three-dimensions (3-D) in vivo. Commonly used two-dimensional (2-D) cell Cultures are inadequate to recreate the biological microenvironment of tumor cells. The potentially different outcomes from 2-D and 3-D culture systems may have a significant impact oil the relevance of experimental findings. The purpose of this study was to characterize the human hepatoma cell line HepG2 in 2-D and 3-D Cultures. HepG2 cells in 2-D and 3-D cultures were treated with cisplatin, 5-fluorouracil, and adriamycin and were analyzed by scanning electron microscopy and transmission electron microscopy. Cell cycle progression and apoptosis were detected by flow cytometry. Inhibition of cell proliferation was quantified by MTT assay. The expression of E-cadherin, CD44v6, VEGF, KDR, endostatin, Bax, and cytochrome-c were analyzed by immunohistochemical (IHC) staining. As compared to the 2-D monolayer culture, the 3-D multicellular spheroids (MCS) of HepG2 cells featured a greater fraction of cells in G I phase and were organized with more abundant cell-cell adhesion. In addition, cells in MCS were significantly less apoptotic in maintenance culture media and were more resistant to drug-induced apoptosis. E-cadherin, CD44v6, VEGF, KDR, endostatin, and cytochrome-c levels were increased in MCS as compared to 2-D cell cultures. In coclusion, MCS conferred differ-entiated phenotypes including increased cell-cell adhesion and G1 phase cell cycle arrest, enhanced cellular resistance to apoptosis, and upregulated angiogenic potential. Based on our data, a multicellular morphological hierarchy may sustain the growth/survival advantages of cancer cells in vivo. Therefore, a 3-D culture system should be the preferred technique for cancer biology investigation.
Keywords
Cell proliferation, COLLAGEN, Elastomer, Electrospun fibers, Fibroblast, LAYERED SILICATE NANOCOMPOSITES, MATRIX, Nanocomposite, ORIENTATION, Osteoblast, OSTEOCLAST, POLYMERIZATION, SCAFFOLDS, STATIC MAGNETIC-FIELD, TISSUE
Cell proliferation, COLLAGEN, Elastomer, Electrospun fibers, Fibroblast, LAYERED SILICATE NANOCOMPOSITES, MATRIX, Nanocomposite, ORIENTATION, Osteoblast, OSTEOCLAST, POLYMERIZATION, SCAFFOLDS, STATIC MAGNETIC-FIELD, TISSUE
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search attributes
CellLine: HEP-G2
Morphology: Cancerous-Hepatoma
Origin: Liver
Species: Human
Scaffold Form: induced aggregate / spheroid formationMorphology: Cancerous-Hepatoma
Origin: Liver
Species: Human

