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Multifunctional Platinum@BSA–Rapamycin Nanocarriers for the Combinatorial Therapy of Cerebral Cavernous Malformation
[Image: see text] Platinum nanoparticles (PtNPs) are antioxidant enzyme-mimetic nanomaterials with significant potential for the treatment of complex diseases related to oxidative stress. Among such diseases, Cerebral Cavernous Malformation (CCM) is a major cerebrovascular disorder of genetic origin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288776/ https://www.ncbi.nlm.nih.gov/pubmed/30556006 http://dx.doi.org/10.1021/acsomega.8b01653 |
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author | De Luca, Elisa Pedone, Deborah Moglianetti, Mauro Pulcini, Daniele Perrelli, Andrea Retta, Saverio Francesco Pompa, Pier Paolo |
author_facet | De Luca, Elisa Pedone, Deborah Moglianetti, Mauro Pulcini, Daniele Perrelli, Andrea Retta, Saverio Francesco Pompa, Pier Paolo |
author_sort | De Luca, Elisa |
collection | PubMed |
description | [Image: see text] Platinum nanoparticles (PtNPs) are antioxidant enzyme-mimetic nanomaterials with significant potential for the treatment of complex diseases related to oxidative stress. Among such diseases, Cerebral Cavernous Malformation (CCM) is a major cerebrovascular disorder of genetic origin, which affects at least 0.5% of the general population. Accumulated evidence indicates that loss-of-function mutations of the three known CCM genes predispose endothelial cells to oxidative stress-mediated dysfunctions by affecting distinct redox-sensitive signaling pathways and mechanisms, including pro-oxidant and antioxidant pathways and autophagy. A multitargeted combinatorial therapy might thereby represent a promising strategy for the effective treatment of this disease. Herein, we developed a multifunctional nanocarrier by combining the radical scavenging activity of PtNPs with the autophagy-stimulating activity of rapamycin (Rapa). Our results show that the combinatorial targeting of redox signaling and autophagy dysfunctions is effective in rescuing major molecular and cellular hallmarks of CCM disease, suggesting its potential for the treatment of this and other oxidative stress-related diseases. |
format | Online Article Text |
id | pubmed-6288776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-62887762018-12-12 Multifunctional Platinum@BSA–Rapamycin Nanocarriers for the Combinatorial Therapy of Cerebral Cavernous Malformation De Luca, Elisa Pedone, Deborah Moglianetti, Mauro Pulcini, Daniele Perrelli, Andrea Retta, Saverio Francesco Pompa, Pier Paolo ACS Omega [Image: see text] Platinum nanoparticles (PtNPs) are antioxidant enzyme-mimetic nanomaterials with significant potential for the treatment of complex diseases related to oxidative stress. Among such diseases, Cerebral Cavernous Malformation (CCM) is a major cerebrovascular disorder of genetic origin, which affects at least 0.5% of the general population. Accumulated evidence indicates that loss-of-function mutations of the three known CCM genes predispose endothelial cells to oxidative stress-mediated dysfunctions by affecting distinct redox-sensitive signaling pathways and mechanisms, including pro-oxidant and antioxidant pathways and autophagy. A multitargeted combinatorial therapy might thereby represent a promising strategy for the effective treatment of this disease. Herein, we developed a multifunctional nanocarrier by combining the radical scavenging activity of PtNPs with the autophagy-stimulating activity of rapamycin (Rapa). Our results show that the combinatorial targeting of redox signaling and autophagy dysfunctions is effective in rescuing major molecular and cellular hallmarks of CCM disease, suggesting its potential for the treatment of this and other oxidative stress-related diseases. American Chemical Society 2018-11-13 /pmc/articles/PMC6288776/ /pubmed/30556006 http://dx.doi.org/10.1021/acsomega.8b01653 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | De Luca, Elisa Pedone, Deborah Moglianetti, Mauro Pulcini, Daniele Perrelli, Andrea Retta, Saverio Francesco Pompa, Pier Paolo Multifunctional Platinum@BSA–Rapamycin Nanocarriers for the Combinatorial Therapy of Cerebral Cavernous Malformation |
title | Multifunctional Platinum@BSA–Rapamycin Nanocarriers
for the Combinatorial Therapy of Cerebral Cavernous Malformation |
title_full | Multifunctional Platinum@BSA–Rapamycin Nanocarriers
for the Combinatorial Therapy of Cerebral Cavernous Malformation |
title_fullStr | Multifunctional Platinum@BSA–Rapamycin Nanocarriers
for the Combinatorial Therapy of Cerebral Cavernous Malformation |
title_full_unstemmed | Multifunctional Platinum@BSA–Rapamycin Nanocarriers
for the Combinatorial Therapy of Cerebral Cavernous Malformation |
title_short | Multifunctional Platinum@BSA–Rapamycin Nanocarriers
for the Combinatorial Therapy of Cerebral Cavernous Malformation |
title_sort | multifunctional platinum@bsa–rapamycin nanocarriers
for the combinatorial therapy of cerebral cavernous malformation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288776/ https://www.ncbi.nlm.nih.gov/pubmed/30556006 http://dx.doi.org/10.1021/acsomega.8b01653 |
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