Evidence map›Paper›PMID 34094902›Full record

ArticleFrontiers in oncology2021

Androgen Receptor, Although Not a Specific Marker For, Is a Novel Target to Suppress Glioma Stem Cells as a Therapeutic Strategy for Glioblastoma.

Nan Zhao, Fei Wang, Shaheen Ahmed, Kan Liu, Chi Zhang, Sahara J Cathcart, Dominick J DiMaio, Michael Punsoni, Bingjie Guan, Ping Zhou and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 74 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

16 authors at 3 institutions in 2 countries.

Nan ZhaoDepartment of Radiation Oncology, Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, United States.
Fei WangDepartment of Radiation Oncology, Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, United States.
Shaheen AhmedDepartment of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE, United States.
Kan LiuSchool of Biological Sciences, University of Nebraska-Lincoln, Lincoln, NE, United States.
Chi ZhangSchool of Biological Sciences, University of Nebraska-Lincoln, Lincoln, NE, United States.
Sahara J CathcartDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, United States.
Dominick J DiMaioDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, United States.
Michael PunsoniDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, United States.
Bingjie GuanDepartment of Radiation Oncology, Union Hospital of Fujian Medical University, Fuzhou, China.
Ping ZhouDepartment of Radiation Oncology, The First Affiliated Hospital of Hainan Medical University, Haikou, China.
Shuo WangDepartment of Radiation Oncology, Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, United States.
Surinder K BatraDepartment of Biochemistry and Molecular Biology, College of Medicine, Eppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha, NE, United States.
Tatiana BronichDepartment of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE, United States.
Tom K HeiCenter for Radiological Research, College of Physicians and Surgeons, Columbia University, New York, NY, United States.
Chi LinDepartment of Radiation Oncology, Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, United States.
Chi ZhangDepartment of Radiation Oncology, Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, United States.
University of Nebraska Medical Center · USUniversity of Nebraska–Lincoln · USFujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting androgen receptor (AR) has been shown to be promising in treating glioblastoma (GBM) in cell culture and flank implant models but the mechanisms remain unclear. AR antagonists including enzalutamide are available for treating prostate cancer patients in clinic and can pass the blood-brain barrier, thus are potentially good candidates for GBM treatment but have not been tested in GBM orthotopically. Our current studies confirmed that in patients, a majority of GBM tumors overexpress AR in both genders. Enzalutamide inhibited the proliferation of GBM cells both

Indexed as

androgen receptorAR antagonistcancer stem cellsenzalutamideglioblastoma

Identifiers

PMID34094902
PMCPMC8175980
OpenAlexW3163079392

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.