Evidence map›Paper›PMID 25821789›Full record

ArticleBioMed research international2015

Combined epidermal growth factor receptor and Beclin1 autophagic protein expression analysis identifies different clinical presentations, responses to chemo- and radiotherapy, and prognosis in glioblastoma.

Paolo Tini, Giuseppe Belmonte, Marzia Toscano, Clelia Miracco, Silvia Palumbo, Pierpaolo Pastina, Giuseppe Battaglia, Valerio Nardone, Marie Aimée Gloria Munezero Butorano, Armando Masucci and 2 more

Open access · hybridAbstract readClinical Study
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. The STAT3-Regulated Autophagy Pathway in Glioblastoma.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  6. Repurposing autophagy regulators in brain tumors.International journal of cancer · 2022
    Review
  7. Review
  8. Review
  9. A Novel Risk Model Based on Autophagy Pathway Related Genes for Survival Prediction in Lung Adenocarcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  10. Autophagy as a Potential Therapy for Malignant Glioma.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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

12 authors at 3 institutions in 1 country.

Paolo TiniTuscan Tumor Institute (ITT), 50139 Florence, Italy ; Unit of Radiation Oncology, University Hospital of Siena, 53100 Siena, Italy ; Department of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy.
Giuseppe BelmonteTuscan Tumor Institute (ITT), 50139 Florence, Italy ; Department of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy ; Unit of Pathological Anatomy, Department of Medicine, Surgery and Neurological Sciences, University of Siena, 53100 Siena, Italy.
Marzia ToscanoTuscan Tumor Institute (ITT), 50139 Florence, Italy ; Department of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy.
Clelia MiraccoTuscan Tumor Institute (ITT), 50139 Florence, Italy ; Department of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy ; Unit of Pathological Anatomy, Department of Medicine, Surgery and Neurological Sciences, University of Siena, 53100 Siena, Italy.
Silvia PalumboDepartment of Biology and Biotechnology, University of Pavia, 27100 Pavia, Italy.
Pierpaolo PastinaTuscan Tumor Institute (ITT), 50139 Florence, Italy ; Department of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy.
Giuseppe BattagliaTuscan Tumor Institute (ITT), 50139 Florence, Italy ; Department of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy.ORCID 0000-0003-3941-5302
Valerio NardoneTuscan Tumor Institute (ITT), 50139 Florence, Italy ; Department of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy.ORCID 0000-0002-7347-0965
Marie Aimée Gloria Munezero ButoranoDepartment of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy ; Unit of Pathological Anatomy, Department of Medicine, Surgery and Neurological Sciences, University of Siena, 53100 Siena, Italy.
Armando MasucciUnit of Preventive Medicine, Moscati Hospital, 83100 Avellino, Italy.
Alfonso CeraseUnit of Neuroradiology, University Hospital of Siena, 53100 Siena, Italy.
Luigi PirtoliTuscan Tumor Institute (ITT), 50139 Florence, Italy ; Unit of Radiation Oncology, University Hospital of Siena, 53100 Siena, Italy ; Department of Medicine, Surgery and Neurological Sciences, Research Center for Molecular Radiobiology, University of Siena, 53100 Siena, Italy.
University of Siena · ITAzienda Ospedaliera S.Giuseppe Moscati · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulated EGFR in glioblastoma may inactivate the key autophagy protein Beclin1. Each of high EGFR and low Beclin1 protein expression, independently, has been associated with tumor progression and poor prognosis. High (H) compared to low (L) expression of EGFR and Beclin1 is here correlated with main clinical data in 117 patients after chemo- and radiotherapy. H-EGFR correlated with low Karnofsky performance and worse neurological performance status, higher incidence of synchronous multifocality, poor radiological evidence of response, shorter progression disease-free (PDFS), and overall survival (OS). H-Beclin1 cases showed better Karnofsky performance status, higher incidence of objective response, longer PDFS, and OS. A mutual strengthening effect emerges in correlative power of stratified L-EGFR and H-Beclin1 expression with incidence of radiological response after treatment, unifocal disease, and better prognosis, thus identifying an even longer OS group (30 months median OS compared to 18 months in L-EGFR, 15 months in H-Beclin1, and 11 months in all GBs) (P = 0.0001). Combined L-EGFR + H-Beclin1 expression may represent a biomarker in identifying relatively favorable clinical presentations and prognosis, thus envisaging possible EGFR/Beclin1-targeted therapies.

Indexed as

AdultAgedAged, 80 and overApoptosis Regulatory ProteinsAutophagyBeclin-1Biomarkers, TumorBrain NeoplasmsChemoradiotherapyErbB ReceptorsGene Expression Regulation, NeoplasticGlioblastomaHumansMembrane ProteinsMiddle AgedPrognosisApoptosis Regulatory ProteinsBeclin-1BECN1 protein, humanBiomarkers, TumorEGFR protein, humanErbB ReceptorsMembrane Proteins

Identifiers

PMID25821789
PMCPMC4363549
OpenAlexW2086476802

What OpenQuestion holds

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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.