Drug delivery to brain tumours: challenges and progress
- PMID: 16822225
- DOI: 10.1517/17425247.3.4.499
Drug delivery to brain tumours: challenges and progress
Abstract
Nearly 12.5 million new cancer cases are diagnosed worldwide each year. Although new treatments have been developed, most new anticancer drugs that are effective outside the brain have failed in clinical trials against brain tumours, in part due to poor penetration across the blood-brain barrier and the blood-brain tumour barrier. This review will discuss the challenges of drug delivery across the blood-brain barrier/blood-brain tumour barrier to cancer cells, as well as progress made so far. This will include a biochemical modulation strategy that transiently opens the barrier to increase anticancer drug delivery selectively to brain tumours. It will also briefly discuss a quantitative non-invasive method to measure permeability changes and tumour response to treatment in the human brain.
Similar articles
-
The targeted delivery of cancer drugs across the blood-brain barrier: chemical modifications of drugs or drug-nanoparticles?Drug Discov Today. 2008 Dec;13(23-24):1099-106. doi: 10.1016/j.drudis.2008.09.005. Epub 2008 Oct 22. Drug Discov Today. 2008. PMID: 18848640 Review.
-
Modulation of the blood-brain barrier in oncology: therapeutic opportunities for the treatment of brain tumours?Cancer Treat Rev. 2004 Aug;30(5):415-23. doi: 10.1016/j.ctrv.2004.04.001. Cancer Treat Rev. 2004. PMID: 15245774 Review.
-
Developing new methods for the treatment of malignant brain tumours: local delivery of anti-neoplastic agents using biodegradable polymers.Forum (Genova). 2000 Apr-Jun;10(2):152-65. Forum (Genova). 2000. PMID: 10875976 Review.
-
Targeted delivery in primary and metastatic brain tumors: summary report of the seventh annual meeting of the Blood-Brain Barrier Disruption Consortium.Clin Cancer Res. 2002 Jun;8(6):1702-9. Clin Cancer Res. 2002. PMID: 12060607
-
Blood-brain barrier disruption in the treatment of brain tumors.Methods Mol Biol. 2011;686:447-63. doi: 10.1007/978-1-60761-938-3_23. Methods Mol Biol. 2011. PMID: 21082387
Cited by
-
Efficient delivery of oncolytic enterovirus by carrier cell line NK-92.Mol Ther Oncolytics. 2021 Apr 1;21:110-118. doi: 10.1016/j.omto.2021.03.013. eCollection 2021 Jun 25. Mol Ther Oncolytics. 2021. PMID: 33981827 Free PMC article.
-
Distinct gene expression profiles between primary breast cancers and brain metastases from pair-matched samples.Sci Rep. 2019 Sep 16;9(1):13343. doi: 10.1038/s41598-019-50099-y. Sci Rep. 2019. PMID: 31527824 Free PMC article.
-
Targeting potassium channels for increasing delivery of imaging agents and therapeutics to brain tumors.Front Pharmacol. 2013 May 29;4:62. doi: 10.3389/fphar.2013.00062. eCollection 2013. Front Pharmacol. 2013. PMID: 23755013 Free PMC article.
-
Targeted delivery of antibody-based therapeutic and imaging agents to CNS tumors: crossing the blood-brain barrier divide.Expert Opin Drug Deliv. 2013 Jul;10(7):907-26. doi: 10.1517/17425247.2013.808184. Epub 2013 Jun 11. Expert Opin Drug Deliv. 2013. PMID: 23751126 Free PMC article. Review.
-
Quantifying Glioblastoma Drug Response Dynamics Incorporating Treatment Sensitivity and Blood Brain Barrier Penetrance From Experimental Data.Front Physiol. 2020 Aug 21;11:830. doi: 10.3389/fphys.2020.00830. eCollection 2020. Front Physiol. 2020. PMID: 32973540 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical