| Literature DB >> 34160805 |
Elisa Taiana1,2, Vanessa Favasuli1,2, Domenica Ronchetti1,2, Eugenio Morelli3, Pierfrancesco Tassone4, Giuseppe Viglietto4, Nikhil C Munshi3, Antonino Neri5,6, Nicola Amodio4.
Abstract
Despite substantial advancements have been achieved in the identification of long noncoding RNA (lncRNA) molecules, many challenges still remain into their functional characterization. Loss-of-function approaches are needed to study oncogenic lncRNAs, which appear more difficult to knock down by RNA interference as compared to mRNAs. In this chapter, we present a protocol based on the use of a novel class of antisense oligonucleotides, named locked nucleic acid (LNA) GapmeRs, to inhibit the oncogenic lncRNA NEAT1 in multiple myeloma cells. Overall, this approach holds many advantages, including its possible independence from delivery reagents as well as the capability to knock down lncRNAs even in hard-to-transfect suspension cells, like hematopoietic cells.Entities:
Keywords: ASO; Electroporation; Gymnosis; LNA-GapmeR; Multiple myeloma cells; lncRNA; ncRNA
Year: 2021 PMID: 34160805 DOI: 10.1007/978-1-0716-1581-2_10
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745