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The microRNA expression associated with morphogenesis of breast cancer cells in three-dimensional organotypic culture.

Authors :
Nguyen HT
Li C
Lin Z
Zhuang Y
Flemington EK
Burow ME
Lin YI
Shan B
Source :
Oncology reports [Oncol Rep] 2012 Jul; Vol. 28 (1), pp. 117-126. Date of Electronic Publication: 2012 Apr 19.
Publication Year :
2012

Abstract

Three-dimensional organotypic culture using reconstituted basement membrane matrix Matrigel (rBM 3-D) is an indispensable tool to characterize morphogenesis of mammary epithelial cells and to elucidate the tumor-modulating actions of extracellular matrix (ECM). microRNAs (miRNAs) are a novel class of oncogenes and tumor suppressors. The majority of our current knowledge of miRNA expression and function in cancer cells is derived from monolayer 2-D culture on plastic substratum, which lacks consideration of the influence of ECM-mediated morphogenesis on miRNAs. In the present study, we compared the expression of miRNAs in rBM 3-D and 2-D cultures of the non-invasive MCF-7 and the invasive MDA-MB231 cells. Our findings revealed a profound difference in miRNA profiles between 2-D and rBM 3-D cultures within each cell type. Moreover, rBM 3-D culture exhibited greater discrimination in miRNA profiles between MCF-7 and MDA-MB231 cells than 2-D culture. The disparate miRNA profiles correlated with distinct mass morphogenesis of MCF-7 and invasive stellate morphogenesis of MDA-MB231 cells in rBM 3-D culture. Supplementation of the tumor promoting type I collagen in rBM 3-D culture substantially altered the miRNA signature of mass morphologenesis of MCF-7 cells in rBM 3-D culture. Overexpression of the differentially expressed miR-200 family member miR429 in MDA-MB231 cells attenuated their invasive stellate morphogenesis in rBM 3-D culture. In summary, we provide the first miRNA signatures of morphogenesis of human breast cancer cells in rBM 3-D culture and warrant further utilization of rBM 3-D culture in investigation of miRNAs in breast cancer.

Details

Language :
English
ISSN :
1791-2431
Volume :
28
Issue :
1
Database :
MEDLINE
Journal :
Oncology reports
Publication Type :
Academic Journal
Accession number :
22576799
Full Text :
https://doi.org/10.3892/or.2012.1764