Cargando…
Rationally engineered nanoparticles target multiple myeloma cells, overcome cell-adhesion-mediated drug resistance, and show enhanced efficacy in vivo
In the continuing search for effective cancer treatments, we report the rational engineering of a multifunctional nanoparticle that combines traditional chemotherapy with cell targeting and anti-adhesion functionalities. Very late antigen-4 (VLA-4) mediated adhesion of multiple myeloma (MM) cells to...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3346680/ https://www.ncbi.nlm.nih.gov/pubmed/22829966 http://dx.doi.org/10.1038/bcj.2012.10 |
_version_ | 1782232206944501760 |
---|---|
author | Kiziltepe, T Ashley, J D Stefanick, J F Qi, Y M Alves, N J Handlogten, M W Suckow, M A Navari, R M Bilgicer, B |
author_facet | Kiziltepe, T Ashley, J D Stefanick, J F Qi, Y M Alves, N J Handlogten, M W Suckow, M A Navari, R M Bilgicer, B |
author_sort | Kiziltepe, T |
collection | PubMed |
description | In the continuing search for effective cancer treatments, we report the rational engineering of a multifunctional nanoparticle that combines traditional chemotherapy with cell targeting and anti-adhesion functionalities. Very late antigen-4 (VLA-4) mediated adhesion of multiple myeloma (MM) cells to bone marrow stroma confers MM cells with cell-adhesion-mediated drug resistance (CAM-DR). In our design, we used micellar nanoparticles as dynamic self-assembling scaffolds to present VLA-4-antagonist peptides and doxorubicin (Dox) conjugates, simultaneously, to selectively target MM cells and to overcome CAM-DR. Dox was conjugated to the nanoparticles through an acid-sensitive hydrazone bond. VLA-4-antagonist peptides were conjugated via a multifaceted synthetic procedure for generating precisely controlled number of targeting functionalities. The nanoparticles were efficiently internalized by MM cells and induced cytotoxicity. Mechanistic studies revealed that nanoparticles induced DNA double-strand breaks and apoptosis in MM cells. Importantly, multifunctional nanoparticles overcame CAM-DR, and were more efficacious than Dox when MM cells were cultured on fibronectin-coated plates. Finally, in a MM xenograft model, nanoparticles preferentially homed to MM tumors with ∼10 fold more drug accumulation and demonstrated dramatic tumor growth inhibition with a reduced overall systemic toxicity. Altogether, we demonstrate the disease driven engineering of a nanoparticle-based drug delivery system, enabling the model of an integrative approach in the treatment of MM. |
format | Online Article Text |
id | pubmed-3346680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33466802012-05-08 Rationally engineered nanoparticles target multiple myeloma cells, overcome cell-adhesion-mediated drug resistance, and show enhanced efficacy in vivo Kiziltepe, T Ashley, J D Stefanick, J F Qi, Y M Alves, N J Handlogten, M W Suckow, M A Navari, R M Bilgicer, B Blood Cancer J Original Article In the continuing search for effective cancer treatments, we report the rational engineering of a multifunctional nanoparticle that combines traditional chemotherapy with cell targeting and anti-adhesion functionalities. Very late antigen-4 (VLA-4) mediated adhesion of multiple myeloma (MM) cells to bone marrow stroma confers MM cells with cell-adhesion-mediated drug resistance (CAM-DR). In our design, we used micellar nanoparticles as dynamic self-assembling scaffolds to present VLA-4-antagonist peptides and doxorubicin (Dox) conjugates, simultaneously, to selectively target MM cells and to overcome CAM-DR. Dox was conjugated to the nanoparticles through an acid-sensitive hydrazone bond. VLA-4-antagonist peptides were conjugated via a multifaceted synthetic procedure for generating precisely controlled number of targeting functionalities. The nanoparticles were efficiently internalized by MM cells and induced cytotoxicity. Mechanistic studies revealed that nanoparticles induced DNA double-strand breaks and apoptosis in MM cells. Importantly, multifunctional nanoparticles overcame CAM-DR, and were more efficacious than Dox when MM cells were cultured on fibronectin-coated plates. Finally, in a MM xenograft model, nanoparticles preferentially homed to MM tumors with ∼10 fold more drug accumulation and demonstrated dramatic tumor growth inhibition with a reduced overall systemic toxicity. Altogether, we demonstrate the disease driven engineering of a nanoparticle-based drug delivery system, enabling the model of an integrative approach in the treatment of MM. Nature Publishing Group 2012-04 2012-04-20 /pmc/articles/PMC3346680/ /pubmed/22829966 http://dx.doi.org/10.1038/bcj.2012.10 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Kiziltepe, T Ashley, J D Stefanick, J F Qi, Y M Alves, N J Handlogten, M W Suckow, M A Navari, R M Bilgicer, B Rationally engineered nanoparticles target multiple myeloma cells, overcome cell-adhesion-mediated drug resistance, and show enhanced efficacy in vivo |
title | Rationally engineered nanoparticles target multiple myeloma cells, overcome
cell-adhesion-mediated drug resistance, and show enhanced efficacy in
vivo |
title_full | Rationally engineered nanoparticles target multiple myeloma cells, overcome
cell-adhesion-mediated drug resistance, and show enhanced efficacy in
vivo |
title_fullStr | Rationally engineered nanoparticles target multiple myeloma cells, overcome
cell-adhesion-mediated drug resistance, and show enhanced efficacy in
vivo |
title_full_unstemmed | Rationally engineered nanoparticles target multiple myeloma cells, overcome
cell-adhesion-mediated drug resistance, and show enhanced efficacy in
vivo |
title_short | Rationally engineered nanoparticles target multiple myeloma cells, overcome
cell-adhesion-mediated drug resistance, and show enhanced efficacy in
vivo |
title_sort | rationally engineered nanoparticles target multiple myeloma cells, overcome
cell-adhesion-mediated drug resistance, and show enhanced efficacy in
vivo |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3346680/ https://www.ncbi.nlm.nih.gov/pubmed/22829966 http://dx.doi.org/10.1038/bcj.2012.10 |
work_keys_str_mv | AT kiziltepet rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo AT ashleyjd rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo AT stefanickjf rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo AT qiym rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo AT alvesnj rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo AT handlogtenmw rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo AT suckowma rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo AT navarirm rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo AT bilgicerb rationallyengineerednanoparticlestargetmultiplemyelomacellsovercomecelladhesionmediateddrugresistanceandshowenhancedefficacyinvivo |