Targeting the undruggable in glioblastoma using nano-based intracellular drug delivery.


Journal

Medical oncology (Northwood, London, England)
ISSN: 1559-131X
Titre abrégé: Med Oncol
Pays: United States
ID NLM: 9435512

Informations de publication

Date de publication:
29 Oct 2024
Historique:
received: 31 07 2024
accepted: 17 10 2024
medline: 29 10 2024
pubmed: 29 10 2024
entrez: 29 10 2024
Statut: epublish

Résumé

Glioblastoma (GBM) is a highly prevalent and aggressive brain tumor in adults with limited treatment response, leading to a 5-year survival rate of less than 5%. Standard therapies, including surgery, radiation, and chemotherapy, often fall short due to the tumor's location, hypoxic conditions, and the challenge of complete removal. Moreover, brain metastases from cancers such as breast and melanoma carry similarly poor prognoses. Recent advancements in nanomedicine offer promising solutions for targeted GBM therapies, with nanoparticles (NPs) capable of delivering chemotherapy drugs or radiation sensitizers across the blood-brain barrier (BBB) to specific tumor sites. Leveraging the enhanced permeability and retention effect, NPs can preferentially accumulate in tumor tissues, where compromised BBB regions enhance delivery efficiency. By modifying NP characteristics such as size, shape, and surface charge, researchers have improved circulation times and cellular uptake, enhancing therapeutic efficacy. Recent studies show that combining photothermal therapy with magnetic hyperthermia using AuNPs and magnetic NPs induces ROS-dependent apoptosis and immunogenic cell death providing dual-targeted, immune-activating approaches. This review discusses the latest NP-based drug delivery strategies, including gene therapy, receptor-mediated transport, and multi-modal approaches like photothermal-magnetic hyperthermia combinations, all aimed at optimizing therapeutic outcomes for GBM.

Identifiants

pubmed: 39470962
doi: 10.1007/s12032-024-02546-8
pii: 10.1007/s12032-024-02546-8
doi:

Substances chimiques

Antineoplastic Agents 0
Nanoparticle Drug Delivery System 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

303

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Sakine Shirvalilou (S)

Finetech in Medicine Research Center, Department of Medical Physics, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Department of Medical Physics, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Samideh Khoei (S)

Finetech in Medicine Research Center, Department of Medical Physics, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Department of Medical Physics, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Reza Afzalipour (R)

Molecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran. reza.afzalipour@hums.ac.ir.
Department of Radiology, Faculty of Para-Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran. reza.afzalipour@hums.ac.ir.

Habib Ghaznavi (H)

Pharmacology Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.

Milad Shirvaliloo (M)

Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Future Science Group, Unitec House, 2 Albert Place, London, N3 1QB, UK.

Zahra Derakhti (Z)

Department of Medical Physics, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Roghayeh Sheervalilou (R)

Pharmacology Research Center, Zahedan University of Medical Sciences, Zahedan, Iran. sheervalilour@tbzmed.ac.ir.

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