» Articles » PMID: 19034673

Epidermal Growth Factor Receptor-targeted Gelatin-based Engineered Nanocarriers for DNA Delivery and Transfection in Human Pancreatic Cancer Cells

Overview
Journal AAPS J
Specialty Pharmacology
Date 2008 Nov 27
PMID 19034673
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Type B gelatin-based engineered nanocarrier systems (GENS) have been used over the last several years as a non-condensing systemic and oral DNA delivery system. In this study, we have modified the surface of GENS with epidermal growth factor receptor (EGFR)-targeting peptide for gene delivery and transfection in pancreatic cancer cell lines. GENS were prepared by the solvent displacement method and the EGFR-targeting peptide was grafted on the surface using a hetero-bifunctional poly(ethylene glycol) (PEG) spacer. Plasmid DNA, encoding for enhanced green fluorescent protein (GFP), was efficiently encapsulated and protected from degrading enzymes in the control and surface-modified GENS. Upon incubation with EGFR over-expressing Panc-1 human pancreatic adenocarcinoma cells, the peptide-modified nanoparticles were found to be internalized efficiently by receptor-mediated endocytosis. Both quantitative and qualitative transgene expression efficiencies were significantly enhanced when plasmid DNA was administered with EGFR-targeted GENS relative to the control-unmodified gelatin or PEG-modified gelatin nanoparticle systems. Based on these preliminary results, EGFR-targeted GENS show tremendous promise as a safe and effective gene delivery vector with the potential to treat pancreatic cancer.

Citing Articles

Gelatin as It Is: History and Modernity.

Mikhailov O Int J Mol Sci. 2023; 24(4).

PMID: 36834993 PMC: 9963746. DOI: 10.3390/ijms24043583.


Nature-Based Biomaterials and Their Application in Biomedicine.

Troy E, Tilbury M, Power A, Wall J Polymers (Basel). 2021; 13(19).

PMID: 34641137 PMC: 8513057. DOI: 10.3390/polym13193321.


Biodegradable Polymeric Nanoparticles for Drug Delivery to Solid Tumors.

Gagliardi A, Giuliano E, Venkateswararao E, Fresta M, Bulotta S, Awasthi V Front Pharmacol. 2021; 12:601626.

PMID: 33613290 PMC: 7887387. DOI: 10.3389/fphar.2021.601626.


GE11 Peptide as an Active Targeting Agent in Antitumor Therapy: A Minireview.

Genta I, Chiesa E, Colzani B, Modena T, Conti B, Dorati R Pharmaceutics. 2017; 10(1).

PMID: 29271876 PMC: 5874815. DOI: 10.3390/pharmaceutics10010002.


Resveratrol-Loaded Albumin Nanoparticles with Prolonged Blood Circulation and Improved Biocompatibility for Highly Effective Targeted Pancreatic Tumor Therapy.

Geng T, Zhao X, Ma M, Zhu G, Yin L Nanoscale Res Lett. 2017; 12(1):437.

PMID: 28673056 PMC: 5493600. DOI: 10.1186/s11671-017-2206-6.


References
1.
Panyam J, Labhasetwar V . Biodegradable nanoparticles for drug and gene delivery to cells and tissue. Adv Drug Deliv Rev. 2003; 55(3):329-47. DOI: 10.1016/s0169-409x(02)00228-4. View

2.
Neves C, Escriou V, Byk G, Scherman D, Wils P . Intracellular fate and nuclear targeting of plasmid DNA. Cell Biol Toxicol. 1999; 15(3):193-202. DOI: 10.1023/a:1007693805849. View

3.
Yamanaka Y, Friess H, Kobrin M, Buchler M, Beger H, Korc M . Coexpression of epidermal growth factor receptor and ligands in human pancreatic cancer is associated with enhanced tumor aggressiveness. Anticancer Res. 1993; 13(3):565-9. View

4.
Roth J . Gene replacement strategies for lung cancer. Curr Opin Oncol. 1998; 10(2):127-32. DOI: 10.1097/00001622-199803000-00008. View

5.
Guillemard V, Nedev H, Berezov A, Murali R, Saragovi H . HER2-mediated internalization of a targeted prodrug cytotoxic conjugate is dependent on the valency of the targeting ligand. DNA Cell Biol. 2005; 24(6):350-8. DOI: 10.1089/dna.2005.24.351. View