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Recent Advances in Nanotherapeutics for Multiple Myeloma

SIMPLE SUMMARY: Nanotherapeutics are useful tools to improve the deliverability of drugs, especially anti-cancer drugs that need to target specific cells. Several approaches have been studied for multiple myeloma, considering that immune cells are not easy to target with the available drugs. These p...

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Autores principales: Iannazzo, Daniela, Ettari, Roberta, Giofrè, Salvatore, Eid, Ali H., Bitto, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693822/
https://www.ncbi.nlm.nih.gov/pubmed/33120945
http://dx.doi.org/10.3390/cancers12113144
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author Iannazzo, Daniela
Ettari, Roberta
Giofrè, Salvatore
Eid, Ali H.
Bitto, Alessandra
author_facet Iannazzo, Daniela
Ettari, Roberta
Giofrè, Salvatore
Eid, Ali H.
Bitto, Alessandra
author_sort Iannazzo, Daniela
collection PubMed
description SIMPLE SUMMARY: Nanotherapeutics are useful tools to improve the deliverability of drugs, especially anti-cancer drugs that need to target specific cells. Several approaches have been studied for multiple myeloma, considering that immune cells are not easy to target with the available drugs. These pharmacological agents are administered in various combinations using Thalidomide (or Lenalidomide, Pomalidomide), corticosteroids (Dexamethasone), proteasome inhibitors (Bortezomib, Carfilzomib, Ixazomib), deacetylase inhibitors (Panobinostat), and monoclonal antibodies (Elotuzumab, Daratumumab). As all drugs these agents might have serious side effects and in addition, the reliance on stochastic events to deliver drugs to tumors reduces their effectiveness either through rapid clearance from blood or inadequate concentration in cancer cells. To address these issues liposomes, micelles, polymeric nanoparticles, inorganic nanoparticles, and carbon-based nanomaterials have been successfully tested in vivo and can be considered as useful tools to improve delivery of active pharmaceuticals that show poor bioavailability or poor internalization into myeloma cells. ABSTRACT: Anticancer therapies cannot be included in a one-size-fits-all scenario; it is imperative to adapt therapies to the tumor molecular profile and most importantly to develop target-specific therapeutics. Nanotherapeutics can combine molecular imaging with molecular therapy in order to provide the maximum benefit to patients in terms of disease prevention, identification, and treatment. Nanotechnology applied to therapy provides numerous advantages in diagnostics and in drug delivery, especially for those malignant cells that are difficult to target or for drugs with poor bioavailability, such as those used for multiple myeloma (MM). This review summarizes the recent advances in the development of nanoparticle-based systems for the treatment of MM, taking into account the methods used for their functionalization, biocompatibility, and anticancer activity.
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spelling pubmed-76938222020-11-28 Recent Advances in Nanotherapeutics for Multiple Myeloma Iannazzo, Daniela Ettari, Roberta Giofrè, Salvatore Eid, Ali H. Bitto, Alessandra Cancers (Basel) Review SIMPLE SUMMARY: Nanotherapeutics are useful tools to improve the deliverability of drugs, especially anti-cancer drugs that need to target specific cells. Several approaches have been studied for multiple myeloma, considering that immune cells are not easy to target with the available drugs. These pharmacological agents are administered in various combinations using Thalidomide (or Lenalidomide, Pomalidomide), corticosteroids (Dexamethasone), proteasome inhibitors (Bortezomib, Carfilzomib, Ixazomib), deacetylase inhibitors (Panobinostat), and monoclonal antibodies (Elotuzumab, Daratumumab). As all drugs these agents might have serious side effects and in addition, the reliance on stochastic events to deliver drugs to tumors reduces their effectiveness either through rapid clearance from blood or inadequate concentration in cancer cells. To address these issues liposomes, micelles, polymeric nanoparticles, inorganic nanoparticles, and carbon-based nanomaterials have been successfully tested in vivo and can be considered as useful tools to improve delivery of active pharmaceuticals that show poor bioavailability or poor internalization into myeloma cells. ABSTRACT: Anticancer therapies cannot be included in a one-size-fits-all scenario; it is imperative to adapt therapies to the tumor molecular profile and most importantly to develop target-specific therapeutics. Nanotherapeutics can combine molecular imaging with molecular therapy in order to provide the maximum benefit to patients in terms of disease prevention, identification, and treatment. Nanotechnology applied to therapy provides numerous advantages in diagnostics and in drug delivery, especially for those malignant cells that are difficult to target or for drugs with poor bioavailability, such as those used for multiple myeloma (MM). This review summarizes the recent advances in the development of nanoparticle-based systems for the treatment of MM, taking into account the methods used for their functionalization, biocompatibility, and anticancer activity. MDPI 2020-10-27 /pmc/articles/PMC7693822/ /pubmed/33120945 http://dx.doi.org/10.3390/cancers12113144 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Iannazzo, Daniela
Ettari, Roberta
Giofrè, Salvatore
Eid, Ali H.
Bitto, Alessandra
Recent Advances in Nanotherapeutics for Multiple Myeloma
title Recent Advances in Nanotherapeutics for Multiple Myeloma
title_full Recent Advances in Nanotherapeutics for Multiple Myeloma
title_fullStr Recent Advances in Nanotherapeutics for Multiple Myeloma
title_full_unstemmed Recent Advances in Nanotherapeutics for Multiple Myeloma
title_short Recent Advances in Nanotherapeutics for Multiple Myeloma
title_sort recent advances in nanotherapeutics for multiple myeloma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693822/
https://www.ncbi.nlm.nih.gov/pubmed/33120945
http://dx.doi.org/10.3390/cancers12113144
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