| Literature DB >> 25652728 |
Ahad Mokhtarzadeh1,2, Hamideh Parhiz1,2, Maryam Hashemi3, Sara Ayatollahi1,2, Khalil Abnous4, Mohammad Ramezani5,6.
Abstract
Specific and effective delivery of drugs and genes to cancer cells are the major issues in successful cancer treatment. Recently, targeted cancer gene therapy has been emerged as a main technology for the treatment of different types of cancers. Among various synthetic carriers, polyethylenimine is one of the most well-known polymers for gene delivery. In this study, we conjugated phage-derived peptide (DMPGTVLP) to polyethylenimine (10 kDa) via disulfide bonds for targeted gene delivery into breast adenocarcinoma cells (MCF-7). As negative-control cells, we used non-related hepatocellular carcinoma cells (HepG2). Peptide-conjugated polyplex exhibited low cytotoxicity and significantly increased the transfection efficiency in comparison with unmodified polyethylenimine. Therefore, the peptide-modified vector can be used as a good targeting agent for gene or drug delivery into breast adenocarcinoma cells.Entities:
Keywords: breast cancer; gene therapy; phage-derived peptide; polyethylenimine
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Year: 2015 PMID: 25652728 PMCID: PMC4674642 DOI: 10.1208/s12249-014-0208-6
Source DB: PubMed Journal: AAPS PharmSciTech ISSN: 1530-9932 Impact factor: 3.246