Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

SHR Neuro Cancer Cardio Lipid Metab Microb

Su, Y; Hu, Y; Wang, Y; Xu, X; Yuan, Y; Li, Y; Wang, Z; Chen, K; Zhang, F; Ding, X; Li, M; Zhou, J; Liu, Y; Wang, W.
A precision-guided MWNT mediated reawakening the sunk synergy in RAS for anti-angiogenesis lung cancer therapy.
Biomaterials. 2017; 139(28):75-90 Doi: 10.1016/j.biomaterials.2017.05.046
Web of Science PubMed FullText FullText_MUG

 

Co-authors Med Uni Graz
Zhang Fangrong
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Multi-walled carbon nanotube (MWNT) with its versatility has exhibited tremendous superiority in drug delivery. Despite plenty of researches on MWNT based delivery systems, precision-guided assistances to maximize their profitable properties are still lacking in substantive progress. We developed here a dual-targeting and co-delivery system based on MWNT for antiangiogenesis therapy in lung cancer which aimed at renin-angiotensin system (RAS) dysregulation by synergistically conducting angiotensin II type 1 receptor (AT1R) and type 2 receptor (AT2R) pathway. In this work, iRGD peptide connected to polyethyleneimine (PEI) was linked to MWNT skeleton, accompanying with candesartan (CD) conjugated to MWNT mediated by cystamine (SS). The functionalized MWNT is assembled with plasmid AT2 (pAT2) to form iRGD-PEI-MWNT-SS-CD/pAT2 complexes. iRGD and CD act as pilots for complexes to dually target symbolic ανβ3-integrin and AT1R both overexpressed on tumor angiogenic endothelium and lung cancer cell. CD as chemotherapy showed synergistic downregulation of VEGF when combining of pAT2 and efficiently inhibited angiogenesis. iRGD-PEI-MWNT-SS-CD/pAT2 complexes greatly appreciated drug activities by changing drug distribution and exhibited remarkable tumor growth suppression in A549 xenograft nude mice. Our work presents that such dual-targeting strategy highly improves the delivery performance of MWNT and open a new avenue for RAS related lung cancer therapy. Copyright © 2017 Elsevier Ltd. All rights reserved.
Find related publications in this database (using NLM MeSH Indexing)
A549 Cells -
Angiogenesis Inhibitors - administration & dosage
Angiogenesis Inhibitors - chemical synthesis
Angiotensin II Type 1 Receptor Blockers - therapeutic use
Animals -
Antineoplastic Agents - administration & dosage
Antineoplastic Agents - chemical synthesis
Benzimidazoles - chemistry
Cystamine - chemistry
Drug Delivery Systems -
Drug Synergism -
Female -
Human Umbilical Vein Endothelial Cells -
Humans -
Lung Neoplasms - blood supply
Lung Neoplasms - drug therapy
Mice -
Mice, Nude -
Nanotubes, Carbon - chemistry
Neovascularization, Pathologic - drug therapy
Oligopeptides - chemistry
Plasmids - chemistry
Polyethyleneimine - chemistry
Receptor, Angiotensin, Type 1 - genetics
Receptor, Angiotensin, Type 1 - metabolism
Receptor, Angiotensin, Type 2 - genetics
Receptor, Angiotensin, Type 2 - metabolism
Renin-Angiotensin System - drug effects
Tetrazoles - chemistry
Vascular Endothelial Growth Factor A - genetics
Vascular Endothelial Growth Factor A - metabolism
Xenograft Model Antitumor Assays -

Find related publications in this database (Keywords)
Multi-walled carbon nanotube
Dual-targeting to lung cancer
RAS related synergistic therapy
Candesartan
Plasmid AT(2)
Anti-angiogenesis therapy
© Med Uni GrazImprint