Evidence map›Paper›PMID 32605912›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Radiation with STAT3 Blockade Triggers Dendritic Cell-T cell Interactions in the Glioma Microenvironment and Therapeutic Efficacy.

Martina Ott, Cynthia Kassab, Anantha Marisetty, Yuuri Hashimoto, Jun Wei, Daniel Zamler, Jia-Shiun Leu, Karl-Heinz Tomaszowski, Aria Sabbagh, Dexing Fang and 10 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 51 citations in OpenAlex.

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  14. Multimodal neuro-nanotechnology: Challenging the existing paradigm in glioblastoma therapy.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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  19. Roles of STAT3 in the pathogenesis and treatment of glioblastoma.Frontiers in cell and developmental biology · 2023
    Review
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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

20 authors at 2 institutions in 1 country.

Martina Ott *Department of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cynthia Kassab *Department of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Anantha Marisetty *Department of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Yuuri HashimotoDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-5934-6060
Jun WeiDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Daniel ZamlerDepartment of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0003-0375-8119
Jia-Shiun LeuDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Karl-Heinz TomaszowskiDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Aria SabbaghDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Dexing FangDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pravesh GuptaDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Waldemar PriebeDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Rafal J ZielinskiDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jared K BurksDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
James P LongDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-5853-5938
Ling-Yuan KongDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Gregory N FullerDepartment of Neuropathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-9447-2647
John DeGrootDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Erik P SulmanDepartment of Radiation Oncology, NYU Langone Health Perlmutter Cancer Center, New York, New York.ORCID 0000-0003-4933-9120
Amy B HeimbergerDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas. aheimber@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USNYU Langone Health · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Tropism Enhanced Oncolytic Adenovirus for the Treatment of Brain TumorsP50CA127001 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Juan Fueyo · 2008 to 2026
$41.2M
UT M.D. Anderson Cancer Center SPORE in MelanomaP50CA093459 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GRIMM, ELIZABETH A · 2004 to 2014
$23.7M
Modulation of Microglia and T Cell Interactions in Malignant GliomaR01CA120813 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HEIMBERGER, AMY BETH, RAO, GANESH · 2007 to 2025
$4.7M
MODELING MALIGNANT PROGRESSION IN GLIOMAR01NS094615 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RAO, GANESH · 2016 to 2020
$1.8M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA093459NCI NIH HHS P50 CA127001NCI NIH HHS R01 CA120813NINDS NIH HHS R01 NS094615
6 · The paper itself

Abstract

purposePatients with central nervous system (CNS) tumors are typically treated with radiotherapy, but this is not curative and results in the upregulation of phosphorylated STAT3 (p-STAT3), which drives invasion, angiogenesis, and immune suppression. Therefore, we investigated the combined effect of an inhibitor of STAT3 and whole-brain radiotherapy (WBRT) in a murine model of glioma. EXPERIMENTAL

designC57BL/6 mice underwent intracerebral implantation of GL261 glioma cells, WBRT, and treatment with WP1066, a blood-brain barrier-penetrant inhibitor of the STAT3 pathway, or the two in combination. The role of the immune system was evaluated using tumor rechallenge strategies, immune-incompetent backgrounds, immunofluorescence, immune phenotyping of tumor-infiltrating immune cells (via flow cytometry), and NanoString gene expression analysis of 770 immune-related genes from immune cells, including those directly isolated from the tumor microenvironment.

resultsThe combination of WP1066 and WBRT resulted in long-term survivors and enhanced median survival time relative to monotherapy in the GL261 glioma model (combination vs. control

conclusionsThis study indicates that the combination of STAT3 inhibition and WBRT enhances the therapeutic effect against gliomas in the CNS by inducing dendritic cell and T-cell interactions in the CNS tumor.

Indexed as

AnimalsAntigen PresentationBrain NeoplasmsCell CommunicationCell Line, TumorChemoradiotherapyDendritic CellsDisease Models, AnimalGliomaHumansImmunologic MemoryMicePyridinesSTAT3 Transcription FactorT-LymphocytesTumor MicroenvironmentPyridinesStat3 protein, mouseSTAT3 Transcription FactorTyrphostinsWP1066

Identifiers

PMID32605912
PMCPMC9341321
OpenAlexW3040064610

What OpenQuestion holds

Textmetadata
LicenceTDM
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.