| Literature DB >> 32394388 |
Lorenzo F Sempere1, Erin Zaluzec2, Elizabeth Kenyon2, Matti Kiupel3, Anna Moore2.
Abstract
microRNAs are an important class of noncoding regulatory RNAs with functional roles in development, physiology, and disease. Visualization of microRNA expression at a single-cell level has contributed to a better understanding of their biological function in animal models and their etiological contribution to human diseases. In addition, several microRNAs have been highlighted as potential biomarkers carrying diagnostic and prognostic information. Co-detection of microRNA expression with that of cell-type-specific proteins can enhance the interpretative power of expression changes during development or altered expression in pathological conditions. Here, we describe an automated fluorescence-based five-color multiplex assay for co-detection of microRNA (e.g., miR-10b, miR-21, miR-205), noncoding RNA (e.g., snRNA U6, 18S rRNA), and protein expression (e.g., cytokeratin 19, vimentin, collagen I) in paraffin-embedded formalin-fixed tissue slides on a Leica Bond Rx staining station. While this protocol uses mainly mouse tissues to demonstrate multiplex detection, it can be generally applied to single-cell expression analysis of other animal models and clinical specimens.Entities:
Keywords: Animal models; Automated staining; Breast cancer; In situ hybridization; Locked nucleic acid (LNA); Molecular pathology; Multiplex detection; Pancreatic cancer; microRNA (miR, miRNA)
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Year: 2020 PMID: 32394388 DOI: 10.1007/978-1-0716-0623-0_17
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745