Evidence map›Paper›PMID 32796101›Full record

ArticleMolecular cancer therapeutics2020

Expression of the Androgen Receptor Governs Radiation Resistance in a Subset of Glioblastomas Vulnerable to Antiandrogen Therapy.

Christian K Werner, Uchechi J Nna, Hanshi Sun, Kari Wilder-Romans, Joseph Dresser, Ayesha U Kothari, Weihua Zhou, Yangyang Yao, Arvind Rao, Stefanie Stallard and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 30 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

26 authors at 6 institutions in 2 countries.

Christian K WernerDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-7496-3617
Uchechi J NnaDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Hanshi SunDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Kari Wilder-RomansDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Joseph DresserDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Ayesha U KothariDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0003-1996-1891
Weihua ZhouDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0003-0259-0828
Yangyang YaoDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Arvind RaoDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Stefanie StallardDepartment of Pediatrics, Michigan Medicine, University of Michigan Medical School, Ann Arbor, Michigan.
Carl KoschmannDepartment of Pediatrics, Michigan Medicine, University of Michigan Medical School, Ann Arbor, Michigan.
Tarik BorDepartment of Cancer Biology, Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, North Carolina.ORCID 0000-0003-0945-4386
Waldemar DebinskiDepartment of Cancer Biology, Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, North Carolina.
Alexander M HegedusDepartment of Climate and Space Sciences and Engineering, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-6247-6934
Meredith A MorganDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Sriram VennetiDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Edwina Baskin-BeyInnocrin Pharmaceuticals, Inc., Durham, North Carolina.
Daniel E SprattDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Howard ColmanDepartment of Neurosurgery, University of Utah, Salt Lake City, Utah.ORCID 0000-0002-4027-7317
Jann N SarkariaDepartment of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
Arul M ChinnaiyanDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Joel R EisnerInnocrin Pharmaceuticals, Inc., Durham, North Carolina.
Corey SpeersDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0002-2362-2860
Theodore S LawrenceDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0002-4186-8821
Roy E StrowdDepartment of Neurology and Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Daniel R WahlDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michigan. dwahl@med.umich.edu.
University of Michigan · USAtrium Health Wake Forest Baptist · USInnocrin Pharmaceuticals (United States) · USMayo Clinic · USUniversity of Utah · USWake Forest University · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
De Novo Nucleotide Synthesis as a Mediator of Radiation Resistance and a Therapeutic Target in GlioblastomaK08CA234416 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WAHL, DANIEL R · 2019 to 2023
$1.1M
Elucidating The Role Of Androgen Receptor (AR) In Mediating Radioresistance In AR-Positive Breast CancerR21CA267147 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SPEERS, COREY W. · 2022 to 2022
$404k
NCATS NIH HHS UL1 TR002240NCI NIH HHS K08 CA234416NCI NIH HHS L30 CA209251NCI NIH HHS P30 CA046592NCI NIH HHS R21 CA267147
6 · The paper itself

Abstract

New approaches are needed to overcome intrinsic therapy resistance in glioblastoma (GBM). Because GBMs exhibit sexual dimorphism and are reported to express steroid hormone receptors, we reasoned that signaling through the androgen receptor (AR) could mediate therapy resistance in GBM, much as it does in AR-positive prostate and breast cancers. We found that nearly half of GBM cell lines, patient-derived xenografts (PDX), and human tumors expressed AR at the transcript and protein level-with expression levels overlapping those of primary prostate cancer. Analysis of gene expression datasets also revealed that AR expression is higher in GBM patient samples than normal brain tissue. Multiple clinical-grade antiandrogens slowed the growth of and radiosensitized AR-positive GBM cell lines and PDXs

Indexed as

Androgen AntagonistsAnimalsFemaleGlioblastomaHumansMiceMice, SCIDReceptors, AndrogenAndrogen AntagonistsReceptors, Androgen

Identifiers

PMID32796101
PMCPMC7842184
OpenAlexW3048664651

What OpenQuestion holds

Textmetadata
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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.