Evidence map›Paper›PMID 21735116›Full record

ArticleJournal of neuro-oncology2012

Prognostic value of novel biomarkers in astrocytic brain tumors: nuclear receptor co-regulators AIB1, TIF2, and PELP1 are associated with high tumor grade and worse patient prognosis.

Zinovia Kefalopoulou, Vassiliki Tzelepi, Vassiliki Zolota, Petros D Grivas, Christos Christopoulos, Haralabos Kalofonos, Theodoros Maraziotis, Georgia Sotiropoulou-Bonikou

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Article in Journal of neuro-oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 43 citations in OpenAlex.

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  18. Journal of Cancer · 2016
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  19. Evidence for involvement of steroid receptors and coactivators in neuroepithelial and meningothelial tumors.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
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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

8 authors at 2 institutions in 2 countries.

Zinovia KefalopoulouDepartment of Pathology, Medical School, University of Patras, 26500 Patras, Greece.
Vassiliki Tzelepi
Vassiliki Zolota
Petros D Grivas
Christos Christopoulos
Haralabos Kalofonos
Theodoros Maraziotis
Georgia Sotiropoulou-Bonikou
University of Patras · GRUniversity of Michigan–Ann Arbor · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen receptors alpha (ERα) and beta (ERβ) and their co-regulatory proteins are key components of complex signaling networks that specifically regulate the growth and development of various tissues and tumors. Still, their protein expression profiles and possible role in the pathogenesis of astrocytic tumors remain largely unknown. The purpose of the present study is to evaluate the differential protein expression of ΕRα, ERβ, and their co-activators, AIB1, TIF2, and PELP1 in astrocytic tumors of World Health Organization (WHO) grade II-IV, using immunohistochemistry. Potential correlations with clinicopathological parameters and patient prognosis were also explored. ERα protein expression was undetectable while ERβ levels were significantly decreased with progression of tumor grade (P < 0.001). High expression of ERβ was an independent favorable prognostic factor on multivariate analysis (P = 0.003). Expression of AIB1, TIF2, and PELP1 was not correlated with ERβ expression and followed an opposite trend, with increasing levels in high-grade relative to low-grade tumors (P < 0.001). Univariate survival analysis revealed that high AIB1, TIF2, and PELP1 expression was associated with worse prognosis (P = 0.049, P = 0.033, and P = 0.020, respectively). ERβ and ER co-activators AIB1, TIF2, and PELP1 appear to play an important role in the pathogenesis and progression of astrocytic tumors and might have prognostic significance. The mechanisms underlying their involvement in astrocytic tumorigenesis, as well as their utility for prognostic and therapeutic purposes merit further investigation.

Indexed as

AdultAnalysis of VarianceAstrocytomaBiomarkers, TumorBrain NeoplasmsCo-Repressor ProteinsEstrogen Receptor betaFemaleHumansImmunohistochemistryKaplan-Meier EstimateMaleMiddle AgedNeoplasm ProteinsNuclear Receptor Coactivator 2Nuclear Receptor Coactivator 3Biomarkers, TumorCo-Repressor ProteinsEstrogen Receptor betaNCOA2 protein, humanNCOA3 protein, humanNeoplasm ProteinsNuclear Receptor Coactivator 2Nuclear Receptor Coactivator 3PELP1 protein, humanTranscription Factors

Identifiers

PMID21735116
OpenAlexW2111476356

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.