Evidence map›Paper›PMID 27409829›Full record

ArticleOncotarget2016

Sex-specific clinicopathological significance of novel (Frizzled-7) and established (MGMT, IDH1) biomarkers in glioblastoma.

Salveena Schiffgens, Ludwig Wilkens, Alba A Brandes, Tatiana Meier, Enrico Franceschi, Mario Ermani, Christian Hartmann, Ibrahim Erol Sandalcioglu, Claudia A Dumitru

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
4.4field-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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 62 citations in OpenAlex.

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  20. Sex Disparities inJournal of clinical medicine · 2021
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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

9 authors at 5 institutions in 2 countries.

Salveena SchiffgensDepartment of Neurosurgery, Nordstadt Hospital Hannover, Hannover, Germany.
Ludwig WilkensDepartment of Pathology, Nordstadt Hospital Hannover, Hannover, Germany.
Alba A BrandesDepartment of Medical Oncology, Bellaria Hospital, AUSL-IRCCS Institute of Neurological Sciences, Bologna, Italy.
Tatiana MeierDepartment of Pathology, Nordstadt Hospital Hannover, Hannover, Germany.
Enrico FranceschiDepartment of Medical Oncology, Bellaria Hospital, AUSL-IRCCS Institute of Neurological Sciences, Bologna, Italy.
Mario ErmaniDepartment of Neurosciences, Statistics and Informatics Unit, University Hospital Padova, Padua, Italy.
Christian HartmannDepartment of Neuropathology, Institute of Pathology, Hannover Medical School, Hannover, Germany.
Ibrahim Erol SandalciogluDepartment of Neurosurgery, Nordstadt Hospital Hannover, Hannover, Germany.
Claudia A DumitruDepartment of Neurosurgery, Nordstadt Hospital Hannover, Hannover, Germany.
KRH Klinikum Nordstadt · DEInstitute of Neurological Sciences · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITMedizinische Hochschule Hannover · DEUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Wnt receptor Frizzled-7 (FZD7) promotes tumor progression and can be currently targeted by monoclonal antibody therapy. Here, we determined the prognostic value of FZD7 for the overall survival of glioblastoma (GBM) patients, both as individual marker and taken in combination with the previously-described markers MGMT and IDH1. Additionally, we tested whether these markers (alone or in combination) exhibited sex-specific differences.

resultsHigh levels of FZD7 (FZD7high) associated with shorter survival in GBM patients; however, FZD7high was a significant predictor of poor survival only in male patients. Mutation of IDH1 significantly associated with longer survival in male but not female patients. Methylated MGMT promoter significantly associated with longer survival only in female patients. Combination of FZD7 with MGMT enhanced the prognostic accuracy and abrogated the sex differences observed upon single marker analysis. Combination of FZD7 with IDH1 was a significant predictor of survival in male GBM patients only. MATERIALS AND

methodsThree independent cohorts of patients with primary GBM (n=120, n=108 and n=105, respectively) were included in this study. FZD7 and IDH1 were assessed by immunohistochemistry in tissue microarrays. MGMT promoter methylation was determined by methylation-specific polymerase chain reaction. Survival analysis was performed by Kaplan-Meier estimate, log-rank test and Cox proportional hazard regression.

conclusionsOur study identifies novel individual and combination markers with prognostic and, possibly, therapeutic relevance in GBM. Furthermore, our findings substantiate the importance of sexual dimorphism in this type of cancer.

Indexed as

AgedBiomarkers, TumorBrain NeoplasmsDNA Modification MethylasesDNA Repair EnzymesFemaleFrizzled ReceptorsGlioblastomaHumansIsocitrate DehydrogenaseMaleMiddle AgedPromoter Regions, GeneticProportional Hazards ModelsSex CharacteristicsTissue Array AnalysisBiomarkers, TumorDNA Modification MethylasesDNA Repair EnzymesFrizzled ReceptorsFZD7 protein, humanIDH1 protein, humanIsocitrate DehydrogenaseMGMT protein, humanTumor Suppressor ProteinsFrizzled-7glioblastomaIDH1MGMTsex-specific biomarkers

Identifiers

PMID27409829
PMCPMC5342409
OpenAlexW2470924809

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Registered trials

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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.