Evidence map›Paper›PMID 25083989›Full record

ArticleThe Journal of clinical investigation2014

Sexually dimorphic RB inactivation underlies mesenchymal glioblastoma prevalence in males.

Tao Sun, Nicole M Warrington, Jingqin Luo, Michael D Brooks, Sonika Dahiya, Steven C Snyder, Rajarshi Sengupta, Joshua B Rubin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed, 3 pooled it
4.5field-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

104 citing papers in PubMed, 3 syntheses or guidelines pooled it, 168 citations in OpenAlex.

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44 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

8 authors.

Tao Sun
Nicole M Warrington
Jingqin Luo
Michael D Brooks
Sonika Dahiya
Steven C Snyder
Rajarshi Sengupta
Joshua B Rubin

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University Center for Translational NeuroscienceP30NS057105 · NINDS · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M. · 2006 to 2011
$8.7M
MOLECULAR BASIS FOR THE IMPACT OF SEX ON BRAIN TUMORIGENESISR01CA174737 · NCI · WASHINGTON UNIVERSITY · PI RUBIN, JOSHUA B · 2014 to 2024
$3.5M
STROMAL CONTRIBUTIONS TO NF1 GLIOMA FORMATION AND GROWTHR01CA136573 · NCI · WASHINGTON UNIVERSITY · PI GUTMANN, DAVID H, RUBIN, JOSHUA B · 2009 to 2013
$1.5M
NCI NIH HHS P30 CA091842NCI NIH HHS P30 CA91842NCI NIH HHS R01 CA136573NCI NIH HHS R01 CA174737NINDS NIH HHS P30 NS057105
6 · The paper itself

Abstract

The prevalence of brain tumors in males is common but unexplained. While sex differences in disease are typically mediated through acute sex hormone actions, sex-specific differences in brain tumor rates are comparable at all ages, suggesting that factors other than sex hormones underlie this discrepancy. We found that mesenchymal glioblastoma (Mes-GBM) affects more males as the result of cell-intrinsic sexual dimorphism in astrocyte transformation. We used astrocytes from neurofibromin-deficient (Nf1(-/-)) mice expressing a dominant-negative form of the tumor suppressor p53 (DNp53) and treated them with EGF as a Mes-GBM model. Male Mes-GBM astrocytes exhibited greater growth and colony formation compared with female Mes-GBM astrocytes. Moreover, male Mes-GBM astrocytes underwent greater tumorigenesis in vivo, regardless of recipient mouse sex. Male Mes-GBM astrocytes exhibited greater inactivation of the tumor suppressor RB, higher proliferation rates, and greater induction of a clonogenic, stem-like cell population compared with female Mes-GBM astrocytes. Furthermore, complete inactivation of RB and p53 in Mes-GBM astrocytes resulted in equivalent male and female tumorigenic transformation, indicating that intrinsic differences in RB activation are responsible for the predominance of tumorigenic transformation in male astrocytes. Together, these results indicate that cell-intrinsic sex differences in RB regulation and stem-like cell function may underlie the predominance of GBM in males.

Indexed as

AnimalsAstrocytesBrain NeoplasmsCell Transformation, NeoplasticErbB ReceptorsExtracellular Signal-Regulated MAP KinasesGenes, Neurofibromatosis 1Genes, p53GlioblastomaHumansMaleMicePhosphorylationPrevalenceRetinoblastoma ProteinSex CharacteristicsErbB ReceptorsExtracellular Signal-Regulated MAP KinasesRetinoblastoma Protein

Identifiers

PMID25083989
PMCPMC4151215
OpenAlexW2158249814

What OpenQuestion holds

Textmetadata
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.