Evidence map›Paper›PMID 39023794›Full record

ReviewMolecular neurobiology2025

Role of Non-coding RNAs in the Response of Glioblastoma to Temozolomide.

Pouya Goleij, Ghazaleh Pourali, Arash Raisi, Fatemeh Ravaei, Shahin Golestan, Atena Abed, Zahra Sadat Razavi, Fatemeh Zarepour, Seyed Pouya Taghavi, Sahar Ahmadi Asouri and 6 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

16 authors.

Pouya GoleijDepartment of Genetics, Faculty of Biology, Sana Institute of Higher Education, Sari, Iran.
Ghazaleh PouraliMetabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Arash RaisiSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Fatemeh RavaeiSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Shahin GolestanDepartment of Ophthalmology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Atena AbedDepartment of Medical Biotechnology, School of Advanced Technologies, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Zahra Sadat RazaviSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Fatemeh ZarepourSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Seyed Pouya TaghaviSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Sahar Ahmadi AsouriResearch Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran.
Moein RafieiSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Seyed Mojtaba MousaviDepartment of Neuroscience and Addiction Studies, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Michael R HamblinResearch Centre, Faculty of Health Science, University of Johannesburg, Doornfontein, 2028, South Africa.
Sahand TaleiSchool of Medicine, Tehran University of Medical Sciences, Tehran, Iran. sahandtalei2@gmail.com.
Amirhossein SheidaSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran. sheidaamirhossein@gmail.com.
Hamed MirzaeiSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran. mirzaei-h@kaums.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy and radiotherapy are widely used in clinical practice across the globe as cancer treatments. Intrinsic or acquired chemoresistance poses a significant problem for medical practitioners and researchers, causing tumor recurrence and metastasis. The most dangerous kind of malignant brain tumor is called glioblastoma multiforme (GBM) that often recurs following surgery. The most often used medication for treating GBM is temozolomide chemotherapy; however, most patients eventually become resistant. Researchers are studying preclinical models that accurately reflect human disease and can be used to speed up drug development to overcome chemoresistance in GBM. Non-coding RNAs (ncRNAs) have been shown to be substantial in regulating tumor development and facilitating treatment resistance in several cancers, such as GBM. In this work, we mentioned the mechanisms of how different ncRNAs (microRNAs, long non-coding RNAs, circular RNAs) can regulate temozolomide chemosensitivity in GBM. We also address the role of these ncRNAs encapsulated inside secreted exosomes.

Indexed as

Antineoplastic Agents, AlkylatingBrain NeoplasmsGlioblastomaRNA, UntranslatedTemozolomideAnimalsDrug Resistance, NeoplasmHumansRNA, Long NoncodingAntineoplastic Agents, AlkylatingRNA, Long NoncodingRNA, UntranslatedTemozolomideChemosensitivityCircular RNAsExosomal Non-coding RNAsGlioblastoma MultiformeLong Non-coding RNAsMicroRNAsTemozolomide

Identifiers

PMID39023794

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.