Evidence map›Paper›PMID 41881949›Full record

ArticleCell death & disease2026

Glioblastoma cells that evade chemoradiotherapy-induced cell death exhibit a bifurcated glycolytic program.

Emma Martell, Helgi Kuzmychova, Ujala Chawla, Akaljot Grewal, Charul Jain, Chitra Venugopal, Christopher M Anderson, Sheila K Singh, Tanveer Sharif

Abstract read
In one paragraph

Article in Cell death & disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Emma Martell *Department of Pathology, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.ORCID http://orcid.org/0009-0008-3985-0703
Helgi Kuzmychova *Department of Pathology, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.ORCID http://orcid.org/0009-0005-5260-349X
Ujala ChawlaDepartment of Pathology, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Akaljot GrewalDepartment of Pathology, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Charul JainDepartment of Pathology, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Chitra VenugopalDepartment of Surgery, McMaster University, Hamilton, ON, Canada.
Christopher M AndersonDepartment of Pharmacology and Therapeutics, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Sheila K SinghDepartment of Surgery, McMaster University, Hamilton, ON, Canada.ORCID http://orcid.org/0000-0003-1272-5300
Tanveer SharifDepartment of Pathology, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada. Tanveer.Sharif@umanitoba.ca.ORCID http://orcid.org/0000-0003-3269-8100

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM), the most common malignant brain tumor in adults, remains a highly lethal and incurable cancer, with a 5-year survival rate below 10%. Standard-of-care involves surgical resection followed by concurrent temozolomide chemotherapy and radiation treatment. While these interventions can effectively shrink tumors, they fail to eradicate all malignant cells. Small populations of GBM cells invariably survive and seed recurrent disease, leading to near-universal relapse and the formation of fatal recurrent tumors, typically within 1-2 years of treatment. Here, we investigated the metabolic features that define these surviving cell populations using ten patient-derived GBM models and matched orthotopic xenograft models exposed to a clinically relevant chemoradiotherapy regimen. By sampling living cells at defined treatment intervals and integrating

Indexed as

Brain NeoplasmsChemoradiotherapyGlioblastomaGlycolysisAnimalsCell DeathCell Line, TumorGlucoseHumansMetabolic ReprogrammingMiceXenograft Model Antitumor AssaysGlucose

Identifiers

PMID41881949
PMCPMC13039382

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.