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Innovative Therapeutic Strategies for Effective Treatment of Brain Metastases
Brain metastases are the most prevalent of intracranial malignancies. They are associated with a very poor prognosis and near 100% mortality. This has been the case for decades, largely because we lack effective therapeutics to augment surgery and radiotherapy. Notwithstanding improvements in the pr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471202/ https://www.ncbi.nlm.nih.gov/pubmed/30875730 http://dx.doi.org/10.3390/ijms20061280 |
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author | Lim, Malcolm Puttick, Simon Houston, Zachary H. Thurecht, Kristofer J. Kalita-de Croft, Priyakshi Mahler, Stephen Rose, Stephen E. Jeffree, Rosalind L. Mazzieri, Roberta Dolcetti, Riccardo Lakhani, Sunil R. Saunus, Jodi M. |
author_facet | Lim, Malcolm Puttick, Simon Houston, Zachary H. Thurecht, Kristofer J. Kalita-de Croft, Priyakshi Mahler, Stephen Rose, Stephen E. Jeffree, Rosalind L. Mazzieri, Roberta Dolcetti, Riccardo Lakhani, Sunil R. Saunus, Jodi M. |
author_sort | Lim, Malcolm |
collection | PubMed |
description | Brain metastases are the most prevalent of intracranial malignancies. They are associated with a very poor prognosis and near 100% mortality. This has been the case for decades, largely because we lack effective therapeutics to augment surgery and radiotherapy. Notwithstanding improvements in the precision and efficacy of these life-prolonging treatments, with no reliable options for adjunct systemic therapy, brain recurrences are virtually inevitable. The factors limiting intracranial efficacy of existing agents are both physiological and molecular in nature. For example, heterogeneous permeability, abnormal perfusion and high interstitial pressure oppose the conventional convective delivery of circulating drugs, thus new delivery strategies are needed to achieve uniform drug uptake at therapeutic concentrations. Brain metastases are also highly adapted to their microenvironment, with complex cross-talk between the tumor, the stroma and the neural compartments driving speciation and drug resistance. New strategies must account for resistance mechanisms that are frequently engaged in this milieu, such as HER3 and other receptor tyrosine kinases that become induced and activated in the brain microenvironment. Here, we discuss molecular and physiological factors that contribute to the recalcitrance of these tumors, and review emerging therapeutic strategies, including agents targeting the PI3K axis, immunotherapies, nanomedicines and MRI-guided focused ultrasound for externally controlling drug delivery. |
format | Online Article Text |
id | pubmed-6471202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64712022019-04-26 Innovative Therapeutic Strategies for Effective Treatment of Brain Metastases Lim, Malcolm Puttick, Simon Houston, Zachary H. Thurecht, Kristofer J. Kalita-de Croft, Priyakshi Mahler, Stephen Rose, Stephen E. Jeffree, Rosalind L. Mazzieri, Roberta Dolcetti, Riccardo Lakhani, Sunil R. Saunus, Jodi M. Int J Mol Sci Review Brain metastases are the most prevalent of intracranial malignancies. They are associated with a very poor prognosis and near 100% mortality. This has been the case for decades, largely because we lack effective therapeutics to augment surgery and radiotherapy. Notwithstanding improvements in the precision and efficacy of these life-prolonging treatments, with no reliable options for adjunct systemic therapy, brain recurrences are virtually inevitable. The factors limiting intracranial efficacy of existing agents are both physiological and molecular in nature. For example, heterogeneous permeability, abnormal perfusion and high interstitial pressure oppose the conventional convective delivery of circulating drugs, thus new delivery strategies are needed to achieve uniform drug uptake at therapeutic concentrations. Brain metastases are also highly adapted to their microenvironment, with complex cross-talk between the tumor, the stroma and the neural compartments driving speciation and drug resistance. New strategies must account for resistance mechanisms that are frequently engaged in this milieu, such as HER3 and other receptor tyrosine kinases that become induced and activated in the brain microenvironment. Here, we discuss molecular and physiological factors that contribute to the recalcitrance of these tumors, and review emerging therapeutic strategies, including agents targeting the PI3K axis, immunotherapies, nanomedicines and MRI-guided focused ultrasound for externally controlling drug delivery. MDPI 2019-03-14 /pmc/articles/PMC6471202/ /pubmed/30875730 http://dx.doi.org/10.3390/ijms20061280 Text en © 2019 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 Lim, Malcolm Puttick, Simon Houston, Zachary H. Thurecht, Kristofer J. Kalita-de Croft, Priyakshi Mahler, Stephen Rose, Stephen E. Jeffree, Rosalind L. Mazzieri, Roberta Dolcetti, Riccardo Lakhani, Sunil R. Saunus, Jodi M. Innovative Therapeutic Strategies for Effective Treatment of Brain Metastases |
title | Innovative Therapeutic Strategies for Effective Treatment of Brain Metastases |
title_full | Innovative Therapeutic Strategies for Effective Treatment of Brain Metastases |
title_fullStr | Innovative Therapeutic Strategies for Effective Treatment of Brain Metastases |
title_full_unstemmed | Innovative Therapeutic Strategies for Effective Treatment of Brain Metastases |
title_short | Innovative Therapeutic Strategies for Effective Treatment of Brain Metastases |
title_sort | innovative therapeutic strategies for effective treatment of brain metastases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471202/ https://www.ncbi.nlm.nih.gov/pubmed/30875730 http://dx.doi.org/10.3390/ijms20061280 |
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