Evidence map›Paper›PMID 26035292›Full record

ReviewInternational journal of oncology2015

Regulation of expression of O6-methylguanine-DNA methyltransferase and the treatment of glioblastoma (Review).

Giulio Cabrini, Enrica Fabbri, Cristiana Lo Nigro, Maria Cristina Dechecchi, Roberto Gambari

Open access · hybridAbstract readReview
In one paragraph

Review in International journal of oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 3 pooled it
6.6field-weighted citation impact, top 3% 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

66 citing papers in PubMed, 3 syntheses or guidelines pooled it, 138 citations in OpenAlex.

  1. Pooled it
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  4. Trial
  5. Cancer genomics & proteomics
    Trial
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  7. Acquired resistance to molecularly targeted therapies for cancer.Cancer drug resistance (Alhambra, Calif.) · 2025
    Review
  8. Genetic and epigenetic landscape of OExploration of targeted anti-tumor therapy · 2025
    Review
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6 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

5 authors at 3 institutions in 1 country.

Giulio CabriniDepartment of Pathology and Diagnostics, University Hospital, Verona, Italy.
Enrica FabbriDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
Cristiana Lo NigroDepartment of Oncology, S. Croce and Carle Teaching Hospital, Cuneo, Italy.
Maria Cristina DechecchiDepartment of Pathology and Diagnostics, University Hospital, Verona, Italy.
Roberto GambariDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
University of Ferrara · ITUniversity of Verona · ITAzienda Sanitaria Ospedaliera S.Croce e Carle Cuneo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

O-6-methylguanine-DNA methyltransferase (MGMT) is an abundantly expressed nuclear protein dealkylating O6-methylguanine (O6-MG) DNA residue, thus correcting the mismatches of O6-MG with a thymine residue during DNA replication. The dealkylating effect of MGMT is relevant not only in repairing DNA mismatches produced by environmental alkylating agents promoting tumor pathogenesis, but also when alkylating molecules are applied in the chemotherapy of different cancers, including glioma, the most common primary tumor of the central nervous system. Elevated MGMT gene expression is known to confer resistance to the treatment with the alkylating drug temozolomide in patients affected by gliomas and, on the contrary, methylation of MGMT gene promoter, which causes reduction of MGMT protein expression, is known to predict a favourable response to temozolomide. Thus, detecting expression levels of MGMT gene is crucial to indicate the option of alkylating agents or to select patients directly for a second line targeted therapy. Further study is required to gain insights into MGMT expression regulation, that has attracted growing interest recently in MGMT promoter methylation, histone acetylation and microRNAs expression. The review will focus on the epigenetic regulation of MGMT gene, with translational applications to the identification of biomarkers predicting response to therapy and prognosis.

Indexed as

Drug Resistance, NeoplasmEpigenesis, GeneticBiomarkers, TumorDacarbazineDNA MethylationDNA Modification MethylasesDNA Repair EnzymesGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticGlioblastomaHumansPromoter Regions, GeneticTemozolomideTumor Suppressor ProteinsBiomarkers, TumorDacarbazineDNA Modification MethylasesDNA Repair EnzymesMGMT protein, humanTemozolomideTumor Suppressor Proteins

Identifiers

PMID26035292
PMCPMC4501657
OpenAlexW1573845599

What OpenQuestion holds

Textmetadata
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.