| Literature DB >> 23988358 |
Anthony Maina1, Brittany A Blackman, Christopher J Parronchi, Eva Morozko, Maria E Bender, Allan D Blake, David Sabatino.
Abstract
Linear, branch and hyperbranch siRNAs were effectively prepared for down-regulating GRP78 expression and inducing cell death in HepG2 liver cancer cells. Branch and hyperbranch GRP78 siRNAs were synthesized by automated solid-phase synthesis in good yields (44-78%) and isolated in excellent purities (>99%) following HPLC purification. Moreover, siRNAs adopted stable intramolecular hybrids as discerned by native PAGE and thermal denaturation studies. These sequences also exhibited the pre-requisite A-type helical trajectory for triggering RNAi activity as determined by CD spectroscopy. Biological studies confirmed potent suppression of GRP78 expression (50-60%) while compromising cancer cell viability by ~20%. Thus, branch and hyperbranch siRNAs may serve as potent siRNA candidates in cancer gene therapy applications. Published by Elsevier Ltd.Entities:
Keywords: Branch siRNA; GRP78 silencing; Hyperbranch siRNA; Oncogene therapy; RNAi
Mesh:
Substances:
Year: 2013 PMID: 23988358 DOI: 10.1016/j.bmcl.2013.08.033
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823