Evidence map›Paper›PMID 29533842›Full record

ArticleColloids and surfaces. B, Biointerfaces2018

pH driven precipitation of quisinostat onto PLA-PEG nanoparticles enables treatment of intracranial glioblastoma.

Kyle T Householder, Danielle M DiPerna, Eugene P Chung, Anne Rosa Luning, Duong T Nguyen, Sarah E Stabenfeldt, Shwetal Mehta, Rachael W Sirianni

Open access · hybridAbstract read
In one paragraph

Article in Colloids and surfaces. B, Biointerfaces, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Kyle T HouseholderBarrow Brain Tumor Research Center, Barrow Neurological Institute, 350 W. Thomas Rd, Phoenix, AZ, 85013, USA; School of Biological and Health Systems Engineering, Ira A. Fulton Schools of Engineering, Arizona State University, P.O. Box 879709, Tempe, AZ, 85287, USA.
Danielle M DiPernaBarrow Brain Tumor Research Center, Barrow Neurological Institute, 350 W. Thomas Rd, Phoenix, AZ, 85013, USA.
Eugene P ChungBarrow Brain Tumor Research Center, Barrow Neurological Institute, 350 W. Thomas Rd, Phoenix, AZ, 85013, USA.
Anne Rosa LuningBarrow Brain Tumor Research Center, Barrow Neurological Institute, 350 W. Thomas Rd, Phoenix, AZ, 85013, USA.
Duong T NguyenSchool of Biological and Health Systems Engineering, Ira A. Fulton Schools of Engineering, Arizona State University, P.O. Box 879709, Tempe, AZ, 85287, USA.
Sarah E StabenfeldtSchool of Biological and Health Systems Engineering, Ira A. Fulton Schools of Engineering, Arizona State University, P.O. Box 879709, Tempe, AZ, 85287, USA.
Shwetal MehtaBarrow Brain Tumor Research Center, Barrow Neurological Institute, 350 W. Thomas Rd, Phoenix, AZ, 85013, USA.
Rachael W SirianniBarrow Brain Tumor Research Center, Barrow Neurological Institute, 350 W. Thomas Rd, Phoenix, AZ, 85013, USA; School of Biological and Health Systems Engineering, Ira A. Fulton Schools of Engineering, Arizona State University, P.O. Box 879709, Tempe, AZ, 85287, USA. Electronic address: rachael.sirianni@dignityhealth.org.
Barrow Neurological Institute · USArizona State University · US

Funding

UCLA SPORE in Brain CancerP50CA211015 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Yvonne Yu-Hsuan Chen · 2017 to 2026
$25.2M
Function of TMEM106B in NeurodegenerationR01NS088448 · NINDS · CORNELL UNIVERSITY · PI HU, FENGHUA · 2014 to 2025
$4.2M
Detecting and Treating Traumatic Brain Injury Pathology Progression from the Inside-OutDP2HD084067 · NICHD · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI STABENFELDT, SARAH E · 2014 to 2018
$2.8M
Targeting Olig2 Co-regulators for Malignant Glioma TherapyR01NS088648 · NINDS · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI MEHTA, SHWETAL · 2015 to 2019
$1.7M
NCI NIH HHS P50 CA211015NICHD NIH HHS DP2 HD084067NINDS NIH HHS R01 NS088448NINDS NIH HHS R01 NS088648
6 · The paper itself

Abstract

Histone deacetylases (HDACs) are known to be key enzymes in cancer development and progression through their modulation of chromatin structure and the expression and post-translational modification of numerous proteins. Aggressive dedifferentiated tumors, like glioblastoma, frequently overexpress HDACs, while HDAC inhibition can lead to cell cycle arrest, promote cellular differentiation and induce apoptosis. Although multiple HDAC inhibitors, such as quisinostat, are of interest in oncology due to their potent in vitro efficacy, their failure in the clinic as monotherapies against solid tumors has been attributed to poor delivery. Thus, we were motivated to develop quisinostat loaded poly(D,L-lactide)-b-methoxy poly(ethylene glycol) nanoparticles (NPs) to test their ability to treat orthotopic glioblastoma. In developing our NP formulation, we identified a novel, pH-driven approach for achieving over 9% (w/w) quisinostat loading. We show quisinostat-loaded NPs maintain drug potency in vitro and effectively slow tumor growth in vivo, leading to a prolonged survival compared to control mice.

Indexed as

AnimalsDrug Delivery SystemsGlioblastomaHumansHydrogen-Ion ConcentrationHydroxamic AcidsMicePolyethylene GlycolsHydroxamic AcidsPolyethylene GlycolsquisinostatGlioblastomaHDACNanoparticlepHPLA-PEGQuisinostat (JNJ-26481585)

Identifiers

PMID29533842
PMCPMC6581030
OpenAlexW2791108347

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.