Evidence map›Paper›PMID 42567946›Full record

ArticleEMBO reports2026

Mannose supports lung cancer metabolism during glycolytic limitation.

Theresa Haitzmann, Niklas B Thompson, Hardik Shah, Katharina Schindlmaier, Joseph Jelwan, Thomas O Eichmann, Nia G Hammond, Maia G Clare, Robert B Cameron, Brandon Faubert and 1 more

Abstract read
In one paragraph

Article in EMBO reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Theresa HaitzmannDivision of Pharmacology, Otto Loewi Research Center, Medical University of Graz, Graz, Austria.
Niklas B ThompsonMetabolomics Platform, Comprehensive Cancer Center, The University of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0003-2745-4945
Hardik ShahMetabolomics Platform, Comprehensive Cancer Center, The University of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0001-8408-5686
Katharina SchindlmaierDivision of Pharmacology, Otto Loewi Research Center, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0000-0002-6703-5123
Joseph JelwanDivision of Pharmacology, Otto Loewi Research Center, Medical University of Graz, Graz, Austria.
Thomas O EichmannCore Facility Mass Spectrometry, Medical University of Graz, Graz, Austria.
Nia G HammondDepartment of Medicine, Section of Hematology and Oncology, The University of Chicago, Chicago, IL, USA.
Maia G ClareDepartment of Medicine, Section of Hematology and Oncology, The University of Chicago, Chicago, IL, USA.
Robert B CameronDepartment of Medicine, Section of Hematology and Oncology, The University of Chicago, Chicago, IL, USA.
Brandon FaubertDepartment of Medicine, Section of Hematology and Oncology, The University of Chicago, Chicago, IL, USA. bfaubert@bsd.uchicago.edu.ORCID http://orcid.org/0000-0002-2886-886X
Katharina LeithnerDivision of Pharmacology, Otto Loewi Research Center, Medical University of Graz, Graz, Austria. katharina.leithner@medunigraz.at.ORCID http://orcid.org/0000-0002-8252-9279

Funding

CLINICAL THERAPEUTICST32GM007019 · NIGMS · UNIVERSITY OF CHICAGO · PI Peter Hugh O'Donnell, MARK J RATAIN · 1985 to 2026
$8.7M
Austrian Federal Ministry of Education, Science and Research Marietta Blau Stipend MMC-2023-07001Austrian Marshall Plan Foundation Marshall Plan ScholarshipAustrian Research Association Funding Programme International CommunicationAustrian Science Fund (FWF) DOC129Austrian Science Fund (FWF) P 33508European Molecular Biology Organization (EMBO) 10661Fondation L'Oréal (FondationLOreal) L'Oréal-UNESCO "For Women in Science" Award AustriaHHS | NIH | National Institute of General Medical Sciences (NIGMS) T32 GM007019Medical University of Graz Short Term Travel Fellowship for Young ResearchersNIGMS NIH HHS T32 GM007019Provincial Government of Styria Travel GrantV Foundation for Cancer Research (VFCR) V2024-036
6 · The paper itself

Abstract

Cancer cells frequently show elevated glucose consumption to support proliferation and survival. This led to the assumption that glycolytic inhibitors could be effective in cancer treatment. However, barriers to clinical implementation remain. Adaptive strategies, such as metabolizing alternative nutrients, may play a role. Here, we investigated the use of an understudied sugar, mannose, in lung cancer cells and xenografts. Stable isotope tracing reveals enhanced contribution of mannose to GDP-mannose and GDP-fucose, key glycosylation precursors, upon treatment with the glycolytic inhibitor 2-deoxyglucose (2-DG) or glucose starvation in vitro. Mannose restores the glucose-withdrawal-induced decrease of GDP-mannose and GDP-fucose pools, and partially rescues proliferation upon 2-DG treatment or glucose deprivation.

Indexed as

GlycolysisLung NeoplasmsMannoseAnimalsCell Line, TumorCell ProliferationDeoxyglucoseGlucoseGlycosylationGuanosine Diphosphate MannoseHumansMetabolic ReprogrammingMiceDeoxyglucoseGlucoseGuanosine Diphosphate MannoseMannose

Identifiers

PMID42567946
PMCPMC13601547

What OpenQuestion holds

Textmetadata
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.