Alginate-embedded HuH-7 cells increase - and reduce expression in vitro.

Cancer Cell Int

Gene Therapy Center, Hospital de Clínicas de Porto Alegre, Rua Ramiro Barcelos 2350, Porto Alegre, RS 90035-903 Brazil ; Post-Graduation Program in Child and Adolescent Health, Federal University of Rio Grande do Sul, Porto Alegre, Brazil ; Post-Graduation Program in Genetics and Molecular Biology, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Published: January 2017

Background: Hepatocellular carcinoma is a common cancer, ranking third in cancer-associated deaths. An important cause of cancer patients' mortality is metastasis. At the start of metastasis progression, there is an epithelial-mesenchymal transition, characterized by matrix degradation, junction reductions and vessels formation. HuH-7 is a cell line used in research as an in vitro model for hepatocellular carcinoma. It is known that two-dimensional growth reflects tumor characteristics poorly. In contrast, three-dimensional cultures provide a better approach to the study of tumorigenic potential. The purpose of this work was to mimic a three-dimensional environment in order to assess gene expression of some epithelial-mesenchymal transition and metastasis progression markers in HuH-7 cells and compare them with traditional two-dimensional culture model.

Methods: HuH-7 cells were encapsulated in sodium alginate (three-dimensional model) to be compared with cells grown in two-dimensional flasks. After 4 days in culture, gene expression of , , and was analyzed by PCR and cytoskeleton assessment was performed by rhodamine-phalloidin staining.

Results: Differences were found in gene expression, with a high increment of and reduction. The cytoskeleton morphology also showed differences, with a cytoplasm restricted only near the nuclei in the three-dimensional model.

Conclusions: This work shows the effects of using sodium alginate capsules as a three-dimensional model to the study of HuH-7. Cells in this 3D system show key markers of epithelial-mesenchymal transition, such as overexpression and down-regulation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5209839PMC
http://dx.doi.org/10.1186/s12935-016-0370-xDOI Listing

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