Evidence map›Paper›PMID 33335215›Full record

ArticleScientific reports2020

Involvement of N-methylpurine DNA glycosylase in resistance to temozolomide in patient-derived glioma cells.

Gemma Serrano-Heras, Beatriz Castro-Robles, Carlos M Romero-Sánchez, Blanca Carrión, Rosa Barbella-Aponte, Hernán Sandoval, Tomás Segura

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. The Link Between Human Alkyladenine DNA Glycosylase and Cancer Development.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

7 authors at 1 institution in 1 country.

Gemma Serrano-HerasResearch Unit, Complejo Hospitalario Universitario de Albacete, Laurel, s/n, 02008, Albacete, Spain. gemmas@sescam.jccm.es.
Beatriz Castro-RoblesResearch Unit, Complejo Hospitalario Universitario de Albacete, Laurel, s/n, 02008, Albacete, Spain.
Carlos M Romero-SánchezDepartment of Neurology, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
Blanca CarriónResearch Unit, Complejo Hospitalario Universitario de Albacete, Laurel, s/n, 02008, Albacete, Spain.
Rosa Barbella-AponteDepartment of Anatomical Pathology, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
Hernán SandovalDepartment of Neurosurgery, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
Tomás SeguraDepartment of Neurology, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
Complejo Hospitalario Universitario de Albacete · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy for high-grade astrocytic tumors is mainly based on the use of temozolomide (TMZ), whose efficacy is limited by resistance mechanisms. Despite many investigations pointing to O6-methylguanine-DNA-methyltransferase (MGMT) as being responsible for tumor chemo-resistance, its expression does not predict an accurate response in most gliomas, suggesting that MGMT is not the only determinant of response to treatment. In this sense, several reports indicate that N-methylpurine-DNA-glycosylase (MPG) may be involved in that resistance. With that in mind, we evaluated for the first time the degree of resistance to TMZ treatment in 18 patient-derived glioma cells and its association with MGMT and MPG mRNA levels. Viability cell assays showed that TMZ treatment hardly caused growth inhibition in the patient-derived cells, even in high concentrations, indicating that all primary cultures were chemo-resistant. mRNA expression analyses showed that the TMZ-resistant phenotype displayed by cells is associated with an elevated expression of MPG to a greater extent than it is with transcript levels of MGMT. Our findings suggest that not only is MGMT implicated in resistance to TMZ but MPG, the first enzyme in base excision repair processing, is also involved, supporting its potential role as a target in anti-resistance chemotherapy for astrocytoma and glioblastoma.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Agents, AlkylatingBiomarkers, TumorCell Line, TumorDrug Resistance, NeoplasmFemaleGliomaHumansMaleMiddle AgedNeoplasm GradingNeoplasm StagingO(6)-Methylguanine-DNA MethyltransferaseTemozolomideAntineoplastic Agents, AlkylatingBiomarkers, TumorO(6)-Methylguanine-DNA MethyltransferaseTemozolomide

Identifiers

PMID33335215
PMCPMC7747563
OpenAlexW3110794847

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.