Evidence map›Paper›PMID 29263302›Full record

ArticleJCI insight2017

Addition of carbonic anhydrase 9 inhibitor SLC-0111 to temozolomide treatment delays glioblastoma growth in vivo.

Nathaniel H Boyd, Kiera Walker, Joshua Fried, James R Hackney, Paul C McDonald, Gloria A Benavides, Raffaella Spina, Alessandra Audia, Sarah E Scott, Catherine J Landis and 14 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

66 citing papers in PubMed, 118 citations in OpenAlex.

  1. Article
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  6. IL-22 regulates MASTL expression in intestinal epithelial cells.American journal of physiology. Gastrointestinal and liver physiology · 2024
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6 more citing papers are in PubMed but not listed here.

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

24 authors at 5 institutions in 1 country.

Nathaniel H BoydDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Kiera WalkerDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Joshua FriedDepartment of Oncology, Southern Research Institute, Birmingham, Alabama, USA.
James R HackneyDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Paul C McDonaldDepartment of Integrative Oncology, BC Cancer Research Centre, Vancouver, British Columbia, Canada.
Gloria A BenavidesDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Raffaella SpinaDepartment of Neurological Surgery, Case Western University, Cleveland, Ohio, USA.
Alessandra AudiaDepartment of Translational Molecular Pathology, MD Anderson Cancer Center, Houston, Texas, USA.
Sarah E ScottDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Catherine J LandisDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Anh Nhat TranDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Mark O BevenseeDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Corinne GriguerDepartment of Neurosurgery.
Susan NozellDepartment of Radiation Oncology, and.
G Yancey GillespieDepartment of Neurosurgery.
Burt NaborsDepartment of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Krishna P BhatDepartment of Translational Molecular Pathology, MD Anderson Cancer Center, Houston, Texas, USA.
Eli E BarDepartment of Neurological Surgery, Case Western University, Cleveland, Ohio, USA.
Victor Darley-UsmarDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Bo XuDepartment of Oncology, Southern Research Institute, Birmingham, Alabama, USA.
Emily GordonHudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
Sara J CooperHudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.
Shoukat DedharDepartment of Integrative Oncology, BC Cancer Research Centre, Vancouver, British Columbia, Canada.
Anita B HjelmelandDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
University of Alabama at Birmingham · USHudsonAlpha Institute for Biotechnology · USSouthern Research Institute · USThe Neurological Institute · USThe University of Texas MD Anderson Cancer Center · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OLAF KUTSCH · 1988 to 2026
$84.1M
UAB Neuroscience Core CenterP30NS047466 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI STANDAERT, DAVID G. · 2005 to 2019
$8.5M
CONTEMPORARY THERAPEUTICS FOR ANAPLASTIC GLIOMASP20CA151129 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GILLESPIE, G. YANCEY · 2011 to 2013
$2.3M
Training Program in Brain Tumor BiologyT32NS048039 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BENVENISTE, ETTY N · 2007 to 2017
$2.0M
Targeting Brain Tumor Stem Cells In The Hypoxic MicroenvironmentR01CA187780 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI BAR, ELI E · 2015 to 2019
$1.8M
Cytochrome C Oxidase in Malignant GliomasR01CA160821 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GRIGUER, CORINNE E. · 2012 to 2016
$1.5M
Characterizing the Role of NF-kB in Promoting Glioma TumorigenicityR01CA138517 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NOZELL, SUSAN E · 2010 to 2014
$1.3M
A20 Promotes Glioma Stem Cell Mediated TumorigenesisR01CA151522 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HJELMELAND, ANITA BORTON · 2010 to 2014
$1.2M
Identification of Glucose Transporter 3 Inhibitors for Glioblastoma TreatmentR21NS096531 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AUGELLI-SZAFRAN, CORINNE ELIZABETH, HJELMELAND, ANITA BORTON · 2016 to 2017
$537k
5500 Q-Trap Mass SpectrometerS10RR027822 · NCRR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARNES, STEPHEN · 2010 to 2010
$469k
Paracrine Signaling in Glioma: Bioenergetics Heterogeneity and ChemoresistanceR21NS100054 · NINDS · UNIVERSITY OF IOWA · PI GRIGUER, CORINNE E. · 2016 to 2017
$404k
NCI NIH HHS F31 CA200085NCI NIH HHS P20 CA151129NCI NIH HHS P30 CA013148NCI NIH HHS R01 CA138517NCI NIH HHS R01 CA151522NCI NIH HHS R01 CA160821NCI NIH HHS R01 CA187780NCRR NIH HHS S10 RR027822NIAID NIH HHS P30 AI027767NINDS NIH HHS P30 NS047466NINDS NIH HHS R21 NS096531NINDS NIH HHS R21 NS100054NINDS NIH HHS T32 NS048039
6 · The paper itself

Abstract

Tumor microenvironments can promote stem cell maintenance, tumor growth, and therapeutic resistance, findings linked by the tumor-initiating cell hypothesis. Standard of care for glioblastoma (GBM) includes temozolomide chemotherapy, which is not curative, due, in part, to residual therapy-resistant brain tumor-initiating cells (BTICs). Temozolomide efficacy may be increased by targeting carbonic anhydrase 9 (CA9), a hypoxia-responsive gene important for maintaining the altered pH gradient of tumor cells. Using patient-derived GBM xenograft cells, we explored whether CA9 and CA12 inhibitor SLC-0111 could decrease GBM growth in combination with temozolomide or influence percentages of BTICs after chemotherapy. In multiple GBMs, SLC-0111 used concurrently with temozolomide reduced cell growth and induced cell cycle arrest via DNA damage in vitro. In addition, this treatment shifted tumor metabolism to a suppressed bioenergetic state in vivo. SLC-0111 also inhibited the enrichment of BTICs after temozolomide treatment determined via CD133 expression and neurosphere formation capacity. GBM xenografts treated with SLC-0111 in combination with temozolomide regressed significantly, and this effect was greater than that of temozolomide or SLC-0111 alone. We determined that SLC-0111 improves the efficacy of temozolomide to extend survival of GBM-bearing mice and should be explored as a treatment strategy in combination with current standard of care.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsBrain NeoplasmsCell ProliferationDNA DamageDNA, NeoplasmGlioblastomaHumansHydrogen-Ion ConcentrationMice, NudeNeoplastic Stem CellsPhenylurea CompoundsSulfonamidesTemozolomideXenograft Model Antitumor AssaysDNA, NeoplasmPhenylurea CompoundsSLC-0111SulfonamidesTemozolomideBrain cancerDrug therapyhypoxiaNeuroscienceOncology

Identifiers

PMID29263302
PMCPMC5752277
OpenAlexW2781315337

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.