Targeting VEGF with LNA-stabilized G-rich oligonucleotide for efficient breast cancer inhibition


Autoria(s): Edwards, Stacey L.; Poongavanam, Vasanthanathan; Kanwar, Jagat R.; Roy, Kislay; Hillman, Kristine M.; Prasad, Neerati; Leth-Larsen, Rikke; Petersen, Michael; Marušič, Maja; Plavec, Janez; Wengel, Jesper; Veedu, Rakesh N.
Data(s)

01/01/2015

Resumo

In this study, we investigated the efficacy of an LNA (locked nucleic acid)-modified DNA aptamer named RNV66 targeting VEGF against various breast cancer cell lines. Our results demonstrate that RNV66 efficiently inhibits breast cancer cell proliferation both in vitro and in vivo. Introduction of LNA nucleotides were crucial for higher efficacy. Furthermore, the binding interaction of RNV66 with VEGF was investigated using molecular dynamic simulations leading to the first computational model of the LNA aptamer-VEGF complex blocking its interaction with VEGF-receptor.

Identificador

http://hdl.handle.net/10536/DRO/DU:30077106

Idioma(s)

eng

Publicador

Royal Society of Chemistry

Relação

http://dro.deakin.edu.au/eserv/DU:30077106/kanwar-targetingVEGF-2015.pdf

http://www.dx.doi.org/10.1039/c5cc02756j

http://www.ncbi.nlm.nih.gov/pubmed/25968110

Direitos

2015, Royal Society of Chemistry

Palavras-Chave #Science & Technology #Physical Sciences #Chemistry, Multidisciplinary #Chemistry #LOCKED NUCLEIC-ACID #CYTO-TOXICITY #GROWTH-FACTOR #THERAPEUTICS #APTAMERS #BEVACIZUMAB #ANALOGS
Tipo

Journal Article