Evidence map›Paper›PMID 33846235›Full record

ArticleMolecular cancer therapeutics2021

Dianhydrogalactitol Overcomes Multiple Temozolomide Resistance Mechanisms in Glioblastoma.

Miguel Jiménez-Alcázar, Álvaro Curiel-García, Paula Nogales, Javier Perales-Patón, Alberto J Schuhmacher, Marcos Galán-Ganga, Lucía Zhu, Scott W Lowe, Fátima Al-Shahrour, Massimo Squatrito

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Updates in IDH-Wildtype Glioblastoma.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  10. New Approaches to Glioblastoma.Annual review of medicine · 2022
    Review
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

10 authors at 2 institutions in 2 countries.

Miguel Jiménez-AlcázarSeve Ballesteros Foundation-Brain Tumors Group, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain.
Álvaro Curiel-GarcíaSeve Ballesteros Foundation-Brain Tumors Group, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain.ORCID 0000-0001-6249-3267
Paula NogalesSeve Ballesteros Foundation-Brain Tumors Group, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain.ORCID 0000-0002-6965-6724
Javier Perales-PatónBioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID 0000-0003-0780-6683
Alberto J SchuhmacherSeve Ballesteros Foundation-Brain Tumors Group, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain.ORCID 0000-0002-0136-1049
Marcos Galán-GangaSeve Ballesteros Foundation-Brain Tumors Group, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain.
Lucía ZhuBrain Metastasis Group, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain.
Scott W LoweCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-5284-9650
Fátima Al-ShahrourBioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID 0000-0003-2373-769X
Massimo SquatritoSeve Ballesteros Foundation-Brain Tumors Group, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain. msquatrito@cnio.es.
Spanish National Cancer Research Centre · ESMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most frequent and aggressive primary tumor type in the central nervous system in adults. Resistance to chemotherapy remains one of the major obstacles in GBM treatment. Identifying and overcoming the mechanisms of therapy resistance is instrumental to develop novel therapeutic approaches for patients with GBM. To determine the major drivers of temozolomide (TMZ) sensitivity, we performed shRNA screenings in GBM lines with different O6-methylguanine-DNA methyl-transferase (MGMT) status. We then evaluated dianhydrogalactitol (Val-083), a small alkylating molecule that induces interstrand DNA crosslinking, as a potential treatment to bypass TMZ-resistance mechanisms. We found that loss of mismatch repair (MMR) components and MGMT expression are mutually exclusive mechanisms driving TMZ resistance

Indexed as

AnimalsCell Line, TumorDianhydrogalactitolDrug Resistance, NeoplasmGlioblastomaHumansMiceTemozolomideTransfectionXenograft Model Antitumor AssaysDianhydrogalactitolTemozolomide

Identifiers

PMID33846235
PMCPMC9377222
OpenAlexW3154616075

What OpenQuestion holds

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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.