Evidence map›Paper›PMID 37267108›Full record

ArticleCell reports2023

Mutant IDH regulates glycogen metabolism from early cartilage development to malignant chondrosarcoma formation.

Sinthu Pathmanapan, Raymond Poon, Tomasa Barrientos De Renshaw, Puviindran Nadesan, Makoto Nakagawa, Gireesh A Seesankar, Adrian Kwan Ho Loe, Hongyuan H Zhang, Joan J Guinovart, Jordi Duran and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Skeletal stem cell lineages in osteosarcoma and bone metastasis.Journal of bone and mineral metabolism · 2026
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  11. Diagnostics ofDiagnostics (Basel, Switzerland) · 2024
    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

13 authors at 6 institutions in 3 countries.

Sinthu PathmanapanDevelopmental and Stem Cell Biology, Hospital for Sick Children, Toronto, ON, Canada; Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
Raymond PoonDevelopmental and Stem Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
Tomasa Barrientos De RenshawDepartment of Orthopaedic Surgery, Duke University, Durham, NC, USA.
Puviindran NadesanDepartment of Orthopaedic Surgery, Duke University, Durham, NC, USA.
Makoto NakagawaDepartment of Orthopaedic Surgery, Duke University, Durham, NC, USA.
Gireesh A SeesankarDevelopmental and Stem Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
Adrian Kwan Ho LoeDevelopmental and Stem Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
Hongyuan H ZhangDepartment of Orthopaedic Surgery, Duke University, Durham, NC, USA.
Joan J GuinovartInstitute for Research in Biomedicine (IRB Barcelona) Barcelona, Barcelona, Spain.
Jordi DuranInstitute for Research in Biomedicine (IRB Barcelona) Barcelona, Barcelona, Spain.
Christopher B NewgardDepartment of Pharmacology & Cancer Biology, Duke University, Durham, NC, USA; Sarah W. Stedman Nutrition and Metabolism Center and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC, USA.
Jay S WunderLunenfeld-Tanenbaum Research Institute and the University Musculoskeletal Oncology Unit, Mount Sinai Hospital, Toronto, ON, Canada.
Benjamin A AlmanDepartment of Orthopaedic Surgery, Duke University, Durham, NC, USA. Electronic address: ben.alman@duke.edu.
Duke University Hospital · USHospital for Sick Children · CADuke University · USInstitute for Research in Biomedicine · ESMount Sinai Hospital · CAUniversity of Toronto · CA

Funding

Molecular Etiology of Enchondromatosis: Hedgehog Regulation in ChondrocytesR01AR066765 · NIAMS · DUKE UNIVERSITY · PI ALMAN, BENJAMIN AARON · 2014 to 2025
$3.7M
NIAMS NIH HHS R01 AR066765
6 · The paper itself

Abstract

Chondrosarcomas are the most common malignancy of cartilage and are associated with somatic mutations in isocitrate dehydrogenase 1 (IDH1) and IDH2 genes. Somatic IDH mutations are also found in its benign precursor lesion, enchondromas, suggesting that IDH mutations are early events in malignant transformation. Human mutant IDH chondrosarcomas and mutant Idh mice that develop enchondromas investigated in our studies display glycogen deposition exclusively in mutant cells from IDH mutant chondrosarcomas and Idh1 mutant murine growth plates. Pharmacologic blockade of glycogen utilization induces changes in tumor cell behavior, downstream energetic pathways, and tumor burden in vitro and in vivo. Mutant IDH1 interacts with hypoxia-inducible factor 1α (HIF1α) to regulate expression of key enzymes in glycogen metabolism. Here, we show a critical role for glycogen in enchondromas and chondrosarcomas, which is likely mediated through an interaction with mutant IDH1 and HIF1α.

Indexed as

ChondromaChondrosarcomaIsocitrate DehydrogenaseAnimalsBone NeoplasmsCartilageHumansMiceMutationIsocitrate DehydrogenasecancerchondrosarcomaCP: CancerCP: Metabolismdevelopmentgenetic mutationglycogenmetabolismmutant IDH

Identifiers

PMID37267108
PMCPMC10592452
OpenAlexW4379053944

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.