Matrigel Basement Membrane Matrix influences expression of microRNAs in cancer cell lines

• Published in: Biochemical and biophysical research communications Vol. 427; no. 2; pp. 343 - 348
• Main Authors: Price, Karina J., Tsykin, Anna, Giles, Keith M., Sladic, Rosemary T., Epis, Michael R., Ganss, Ruth, Goodall, Gregory J., Leedman, Peter J.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 19.10.2012
• Subjects: 60 APPLIED LIFE SCIENCES; Cancer; Cell Adhesion - genetics; Cell culture; Cell Culture Techniques; CELL CULTURES; Cell Line, Tumor; CELL PROLIFERATION; Cell Transformation, Neoplastic - genetics; Cell Transformation, Neoplastic - metabolism; Collagen - metabolism; Drug Combinations; Extracellular Matrix - metabolism; Gene Expression Regulation, Neoplastic; Humans; IN VITRO; Laminin - metabolism; LARGE INTESTINE; Matrigel; MESSENGER-RNA; MicroRNA; MicroRNAs - biosynthesis; Neoplasm Invasiveness; NEOPLASMS; Oligonucleotide Array Sequence Analysis; PHENOTYPE; PLASTICS; Proteoglycans - metabolism; Cell culture; MicroRNA; Matrigel; Cancer
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2012.09.059

► Matrigel alters cancer cell line miRNA expression relative to culture on plastic. ► Many identified Matrigel-regulated miRNAs are implicated in cancer. ► miR-1290, -210, -32 and -29b represent a Matrigel-induced miRNA signature. ► miR-32 down-regulates Integrin alpha 5 (ITGA5) mRNA. Matrigel is a medium rich in extracellular matrix (ECM) components used for three-dimensional cell culture and is known to alter cellular phenotypes and gene expression. microRNAs (miRNAs) are small, non-coding RNAs that regulate gene expression and have roles in cancer. While miRNA profiles of numerous cell lines cultured on plastic have been reported, the influence of Matrigel-based culture on cancer cell miRNA expression is largely unknown. This study investigated the influence of Matrigel on the expression of miRNAs that might facilitate ECM-associated cancer cell growth. We performed miRNA profiling by microarray using two colon cancer cell lines (SW480 and SW620), identifying significant differential expression of miRNAs between cells cultured in Matrigel and on plastic. Many of these miRNAs have previously been implicated in cancer-related processes. A common Matrigel-induced miRNA signature comprised of up-regulated miR-1290 and miR-210 and down-regulated miR-29b and miR-32 was identified using RT-qPCR across five epithelial cancer cell lines (SW480, SW620, HT-29, A549 and MDA-MB-231). Experimental modulation of these miRNAs altered expression of their known target mRNAs involved in cell adhesion, proliferation and invasion, in colon cancer cell lines. Furthermore, ITGA5 was identified as a novel putative target of miR-32 that may facilitate cancer cell interactions with the ECM. We propose that culture of cancer cell lines in Matrigel more accurately recapitulates miRNA expression and function in cancer than culture on plastic and thus is a valuable approach to the in vitro study of miRNAs.