Nanomedicine for brain cancer

被引:96
作者
Quader, Sabina [1 ]
Kataoka, Kazunori [1 ]
Cabral, Horacio [2 ]
机构
[1] Kawasaki Inst Ind Promot, Innovat Ctr NanoMed, Kawasaki Ku, 3-25-14 Tonomachi, Kawasaki, Kanagawa 2120821, Japan
[2] Univ Tokyo, Grad Sch Engn, Dept Bioengn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
基金
日本科学技术振兴机构;
关键词
Blood-brain (tumor) barrier; Glioblastoma; Nanocarriers; Transcytosis; Chemotherapy; Immunotherapy; Clinical translation; BLOOD-TUMOR BARRIER; PEGYLATED LIPOSOMAL DOXORUBICIN; CONVECTION-ENHANCED DELIVERY; LOADED POLYMERIC MICELLES; GLIOBLASTOMA CELL-LINES; TARGET RESIDENCE TIME; IN-VIVO MODELS; DRUG-DELIVERY; MALIGNANT GLIOMA; GENE-EXPRESSION;
D O I
10.1016/j.addr.2022.114115
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CNS tumors remain among the deadliest forms of cancer, resisting conventional and new treatment approaches, with mortality rates staying practically unchanged over the past 30 years. One of the primary hurdles for treating these cancers is delivering drugs to the brain tumor site in therapeutic concentration, evading the blood-brain (tumor) barrier (BBB/BBTB). Supramolecular nanomedicines (NMs) are increasingly demonstrating noteworthy prospects for addressing these challenges utilizing their unique characteristics, such as improving the bioavailability of the payloads via controlled pharmacokinetics and pharmacodynamics, BBB/BBTB crossing functions, superior distribution in the brain tumor site, and tumor-specific drug activation profiles. Here, we review NM-based brain tumor targeting approaches to demonstrate their applicability and translation potential from different perspectives. To this end, we provide a general overview of brain tumor and their treatments, the incidence of the BBB and BBTB, and their role on NM targeting, as well as the potential of NMs for promoting superior therapeutic effects. Additionally, we discuss critical issues of NMs and their clinical trials, aiming to bolster the potential clinical applications of NMs in treating these life-threatening diseases. (c) 2022 Elsevier B.V. All rights reserved.
引用
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页数:31
相关论文
共 435 条
[1]   In Vitro and In Vivo Tumor Models for the Evaluation of Anticancer Nanoparticles [J].
Abreu, Teresa R. ;
Biscaia, Mariana ;
Goncalves, Nelio ;
Fonseca, Nuno A. ;
Moreira, Joao Nuno .
BIO-NANOMEDICINE FOR CANCER THERAPY, 2021, 1295 :271-299
[2]   Brain metastases [J].
Achrol, Achal Singh ;
Rennert, Robert C. ;
Anders, Carey ;
Soffietti, Riccardo ;
Ahluwalia, Manmeet S. ;
Nayak, Lakshmi ;
Peters, Solange ;
Arvold, Nils D. ;
Harsh, Griffith R. ;
Steeg, Patricia S. ;
Chang, Steven D. .
NATURE REVIEWS DISEASE PRIMERS, 2019, 5 (1)
[3]   Characterization of passive permeability at the blood-tumor barrier in five preclinical models of brain metastases of breast cancer [J].
Adkins, Chris E. ;
Mohammad, Afroz S. ;
Terrell-Hall, Tori B. ;
Dolan, Emma L. ;
Shah, Neal ;
Sechrest, Emily ;
Griffith, Jessica ;
Lockman, Paul R. .
CLINICAL & EXPERIMENTAL METASTASIS, 2016, 33 (04) :373-383
[4]   Active Efflux of Dasatinib from the Brain Limits Efficacy against Murine Glioblastoma: Broad Implications for the Clinical Use of Molecularly Targeted Agents [J].
Agarwal, Sagar ;
Mittapalli, Rajendar K. ;
Zellmer, David M. ;
Gallardo, Jose L. ;
Donelson, Randy ;
Seiler, Charlie ;
Decker, Stacy A. ;
SantaCruz, Karen S. ;
Pokorny, Jenny L. ;
Sarkaria, Jann N. ;
Elmquist, William F. ;
Ohlfest, John R. .
MOLECULAR CANCER THERAPEUTICS, 2012, 11 (10) :2183-2192
[5]   Nanoparticle-mediated tumor cell expression of mIL-12 via systemic gene delivery treats syngeneic models of murine lung cancers [J].
Ahn, Hye-Hyun ;
Carrington, Christine ;
Hu, Yizong ;
Liu, Heng-Wen ;
Ng, Christy ;
Nam, Hwanhee ;
Park, Andrew ;
Stace, Catherine ;
West, Will ;
Mao, Hai-Quan ;
Pomper, Martin G. ;
Ullman, Christopher G. ;
Minn, Il .
SCIENTIFIC REPORTS, 2021, 11 (01)
[6]   F-Actin Is an Evolutionarily Conserved Damage-Associated Molecular Pattern Recognized by DNGR-1, a Receptor for Dead Cells [J].
Ahrens, Susan ;
Zelenay, Santiago ;
Sancho, David ;
Hanc, Pavel ;
Kjaer, Svend ;
Feest, Christoph ;
Fletcher, Georgina ;
Durkin, Charlotte ;
Postigo, Antonio ;
Skehel, Mark ;
Batista, Facundo ;
Thompson, Barry ;
Way, Michael ;
Sousa, Caetano Reis e ;
Schulz, Oliver .
IMMUNITY, 2012, 36 (04) :635-645
[7]   Challenges to curing primary brain tumours [J].
Aldape, Kenneth ;
Brindle, Kevin M. ;
Chesler, Louis ;
Chopra, Rajesh ;
Gajjar, Amar ;
Gilbert, Mark R. ;
Gottardo, Nicholas ;
Gutmann, David H. ;
Hargrave, Darren ;
Holland, Eric C. ;
Jones, David T. W. ;
Joyce, Johanna A. ;
Kearns, Pamela ;
Kieran, Mark W. ;
Mellinghoff, Ingo K. ;
Merchant, Melinda ;
Pfister, Stefan M. ;
Pollard, Steven M. ;
Ramaswamy, Vijay ;
Rich, Jeremy N. ;
Robinson, Giles W. ;
Rowitch, David H. ;
Sampson, John H. ;
Taylor, Michael D. ;
Workman, Paul ;
Gilbertson, Richard J. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2019, 16 (08) :509-520
[8]   Metabolism of the EGFR tyrosin kinase inhibitor gefitinib by cytochrome P450 1A1 enzyme in EGFR-wild type non small cell lung cancer cell lines [J].
Alfieri, Roberta R. ;
Galetti, Maricla ;
Tramonti, Stefano ;
Andreoli, Roberta ;
Mozzoni, Paola ;
Cavazzoni, Andrea ;
Bonelli, Mara ;
Fumarola, Claudia ;
La Monica, Silvia ;
Galvani, Elena ;
De Palma, Giuseppe ;
Mutti, Antonio ;
Mor, Marco ;
Tiseo, Marcello ;
Mari, Ettore ;
Ardizzoni, Andrea ;
Petronini, Pier Giorgio .
MOLECULAR CANCER, 2011, 10
[9]   Phase 2 trial of temozolomide and pegylated liposomal doxorubicin in the treatment of patients with glioblastoma multiforme following concurrent radiotherapy and chemotherapy [J].
Ananda, Sumitra ;
Nowak, Anna K. ;
Cher, Lawrence ;
Dowling, Anthony ;
Brown, Chris ;
Simes, John ;
Rosenthal, Mark A. .
JOURNAL OF CLINICAL NEUROSCIENCE, 2011, 18 (11) :1444-1448
[10]   Imaging tumor acidosis: a survey of the available techniques for mapping in vivo tumor pH [J].
Anemone, Annasofia ;
Consolino, Lorena ;
Arena, Francesca ;
Capozza, Martina ;
Longo, Dario Livio .
CANCER AND METASTASIS REVIEWS, 2019, 38 (1-2) :25-49