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Aurora kinase inhibitor nanoparticles target tumors with favorable therapeutic index in vivo

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aad2355_ArticleContent_toSPI 15Jan16_MLF.DOCAccepted version1 MBMicrosoft WordView/Open
aad2355_SupplementalMaterial_toSPI 13Jan16_MLF.DOCXSupporting information1.69 MBMicrosoft WordView/Open
Title: Aurora kinase inhibitor nanoparticles target tumors with favorable therapeutic index in vivo
Authors: Ashton, S
Song, YH
Nolan, J
Cadogan, E
Murray, J
Odedra, R
Foster, J
Hall, PA
Low, S
Taylor, P
Ellston, R
Polanska, UM
Wilson, J
Howes, C
Smith, A
Goodwin, RJA
Swales, JG
Strittmatter, N
Takats, Z
Nilsson, A
Andren, P
Trueman, D
Walker, M
Reimer, CL
Troiano, G
Parsons, D
De Witt, D
Ashford, M
Hrkach, J
Zale, S
Jewsbury, PJ
Barry, ST
Item Type: Journal Article
Abstract: A class of drugs, called kinase inhibitors, could stop cancer in its tracks…if only these drugs could reach the tumors, stay for a while, and not be toxic. Hypothesizing that a nanoparticle formulation would solve the inhibitors’ woes, Ashton and colleagues investigated several different compositions of so-called Accurins—polymeric particles that encapsulate charged drugs through ion pairing. An Aurora B kinase, once formulated in Accurins, demonstrated a much-improved therapeutic index and preclinical efficacy compared with its parent molecule, when administered to rats and mice bearing human tumors. The Accurins allowed for sustained release of the drug over days, and did not have the same blood toxicity seen with the parent drug. A phase 1 trial is the next step for this nanomedicine, and additional preclinical studies will reveal whether such nanoformulations can improve the tolerability and efficacy of the broader class of molecularly targeted cancer therapeutics, including cell cycle inhibitors.
Issue Date: 10-Feb-2016
Date of Acceptance: 8-Jan-2016
URI: http://hdl.handle.net/10044/1/37595
DOI: 10.1126/scitranslmed.aad2355
ISSN: 1946-6242
Publisher: American Association for the Advancement of Science
Journal / Book Title: Science Translational Medicine
Volume: 8
Issue: 325
Copyright Statement: Copyright © 2016, Copyright © 2016, American Association for the Advancement of Science. This is the author’s version of the work. It is posted here by permission of the AAAS for personal use, not for redistribution. The definitive version was published in Science Translational Medicine in Volume 8 number 325 10 Feb 2016, DOI: 10.1126/scitranslmed.aad2355
Keywords: Science & Technology
Life Sciences & Biomedicine
Cell Biology
Medicine, Research & Experimental
Research & Experimental Medicine
DOSE CYTOSINE-ARABINOSIDE
B KINASE
BARASERTIB AZD1152
ELDERLY-PATIENTS
SAFETY
TOLERABILITY
FORMULATION
PRODRUG
DRUGS
Science & Technology
Life Sciences & Biomedicine
Cell Biology
Medicine, Research & Experimental
Research & Experimental Medicine
DOSE CYTOSINE-ARABINOSIDE
BARASERTIB AZD1152
ELDERLY-PATIENTS
B KINASE
SAFETY
TOLERABILITY
PRODRUG
Animals
Aurora Kinases
Bone Marrow
Cell Line, Tumor
Drug Liberation
Female
Humans
Male
Mass Spectrometry
Mice
Mice, SCID
Nanoparticles
Organophosphates
Protein Kinase Inhibitors
Quinazolines
Rats, Nude
Treatment Outcome
Xenograft Model Antitumor Assays
Cell Line, Tumor
Bone Marrow
Animals
Humans
Mice
Mice, SCID
Rats, Nude
Quinazolines
Protein Kinase Inhibitors
Treatment Outcome
Xenograft Model Antitumor Assays
Female
Male
Mass Spectrometry
Nanoparticles
Organophosphates
Aurora Kinases
Drug Liberation
06 Biological Sciences
11 Medical and Health Sciences
Publication Status: Published
Article Number: ARTN 325ra17
Appears in Collections:Department of Metabolism, Digestion and Reproduction
Faculty of Medicine