Evidence map›Paper›PMID 28423563›Full record

ArticleOncotarget2017

Regulation of p53wt glioma cell proliferation by androgen receptor-mediated inhibition of small VCP/p97-interacting protein expression.

Dejun Bao, Chuandong Cheng, Xiaoqiang Lan, Rong Xing, Zhuo Chen, Hua Zhao, Junyan Sun, Yang Wang, Chaoshi Niu, Bo Zhang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.3field-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

41 citing papers in PubMed, 60 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

11 authors at 5 institutions in 2 countries.

Dejun BaoDepartment of Neurosurgery, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China.
Chuandong ChengDepartment of Neurosurgery, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China.
Xiaoqiang LanDepartment of Pathophysiology, School of Basic Medical Science, Dalian Medical University, Dalian, China.
Rong XingDepartment of Pathophysiology, School of Basic Medical Science, Dalian Medical University, Dalian, China.
Zhuo ChenAnhui Provincial Cancer Hospital (West Branch of Anhui Provincial Hospital), Hefei, China.
Hua ZhaoDepartment of Clinical Laboratory, Cancer Hospital, Chinese Academy of Science, Hefei, China.
Junyan SunDepartment of Pathophysiology, School of Basic Medical Science, Dalian Medical University, Dalian, China.
Yang WangDepartment of Pathophysiology, School of Basic Medical Science, Dalian Medical University, Dalian, China.
Chaoshi NiuDepartment of Neurosurgery, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China.
Bo ZhangDepartment of Neurosurgery, 2nd Hospital of Dalian Medical University, Dalian, China.
Shengyun FangCenter for Biomedical Engineering and Technology, Department of Physiology, Department of Biochemistry and Molecular Biology, University of Maryland, School of Medicine, Baltimore, Maryland, USA.
Dalian Medical University · CNAnhui Medical University · CNAnhui Provincial Hospital · CNCancer Hospital of Chinese Academy of Medical Sciences · CNUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of glioma in men is higher than that in women; however, little is known about the expression and basic function of the androgen receptor (AR) in gliomas. AR inhibited the small VCP/p97-interacting protein (SVIP) on the transcriptional level was previously reported. The present study shows that the protein level of AR is highly expressed in cell lines of the nervous system. Moreover, the AR expression is increased while SVIP expression is decreased in tumor tissue of glioma patients, which is in agreement with the progressing WHO grades. A statistically significant increase in serum testosterone level of glioma patients compared with that of non-cancer patients was also detected. Furthermore, it has been proved that SVIP is down-regulated as well as AR is up-regulated in glioma cell lines with R1881 treatment. Interestingly, the depletion of SVIP using siRNA facilitated cell proliferation and decreased p53 expression. In addition, overexpression of SVIP increased cell death only in p53wt cell lines. Moreover, U87MG cells, p53wt cell line was susceptible to AR antagonists in vitro and in vivo. The current study provides insight into the biological role of AR in suppressing SVIP and p53 and promoting the progression of glioma as well as the clinical treatment of glioma patients.

Indexed as

Adenosine TriphosphatasesAdultBrain NeoplasmsCell Cycle ProteinsCell Line, TumorCell ProliferationFemaleGene ExpressionGliomaHumansMaleMiddle AgedNeuroblastomaReceptors, AndrogenTestosteroneTumor Suppressor Protein p53Adenosine TriphosphatasesAR protein, humanCell Cycle ProteinsReceptors, AndrogenTestosteroneTP53 protein, humanTumor Suppressor Protein p53Valosin Containing ProteinVCP protein, humanAR signalingcell proliferationp53serum testosteroneSVIP

Identifiers

PMID28423563
PMCPMC5410292
OpenAlexW2588295682

What OpenQuestion holds

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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.