Evidence map›Paper›PMID 31431459›Full record

ArticleCancer research2019

Targeting Glycolysis through Inhibition of Lactate Dehydrogenase Impairs Tumor Growth in Preclinical Models of Ewing Sarcoma.

Choh Yeung, Anna E Gibson, Sameer H Issaq, Nobu Oshima, Joshua T Baumgart, Leah D Edessa, Ganesha Rai, Daniel J Urban, Michelle S Johnson, Gloria A Benavides and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
5.7field-weighted citation impact, top 2% 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

90 citing papers in PubMed, 128 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Targeted and molecular therapies in Ewing sarcoma: a comprehensive review of preclinical and clinical advances.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Glycolysis enzymes and cellular lactylation in tumour.Clinical and translational medicine · 2026
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

30 more citing papers are in PubMed but not listed here.

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

28 authors at 5 institutions in 1 country.

Choh YeungPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Anna E GibsonPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Sameer H IssaqPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Nobu OshimaUrologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Joshua T BaumgartPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Leah D EdessaPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Ganesha RaiChemical Genomics Center, National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland.
Daniel J UrbanChemical Genomics Center, National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland.
Michelle S JohnsonMitochondrial Medicine Laboratory, Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama.
Gloria A BenavidesMitochondrial Medicine Laboratory, Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama.
Giuseppe L SquadritoMitochondrial Medicine Laboratory, Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama.
Marielle E YohePediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Haiyan LeiPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Sandy EldridgeDivision of Cancer Treatment and Diagnosis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.ORCID 0000-0002-7055-2754
John HamreLaboratory of Investigative Toxicology, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Tyrone DowdyNeuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Victor Ruiz-RodadoNeuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Adrian LitaNeuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Arnulfo MendozaPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Jack F ShernPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.ORCID 0000-0001-5579-7625
Mioara LarionNeuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Lee J HelmanPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Gordon M StottLeidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Murali C KrishnaRadiation Biology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Matthew D HallChemical Genomics Center, National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland.ORCID 0000-0002-5073-442X
Victor Darley-UsmarMitochondrial Medicine Laboratory, Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama.
Leonard M NeckersUrologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Christine M HeskePediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland. Christine.heske@nih.gov.
National Institutes of Health · USUniversity of Alabama at Birmingham · USNational Center for Advancing Translational Sciences · USFrederick National Laboratory for Cancer Research · USLeidos (United States) · US

Funding

Development and translation of novel therapies for pediatric sarcomaZIABC011774 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HESKE, CHRISTINE · 2017 to 2025
$9.3M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS ZIA BC011774NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

Altered cellular metabolism, including an increased dependence on aerobic glycolysis, is a hallmark of cancer. Despite the fact that this observation was first made nearly a century ago, effective therapeutic targeting of glycolysis in cancer has remained elusive. One potentially promising approach involves targeting the glycolytic enzyme lactate dehydrogenase (LDH), which is overexpressed and plays a critical role in several cancers. Here, we used a novel class of LDH inhibitors to demonstrate, for the first time, that Ewing sarcoma cells are exquisitely sensitive to inhibition of LDH. EWS-FLI1, the oncogenic driver of Ewing sarcoma, regulated LDH A (LDHA) expression. Genetic depletion of LDHA inhibited proliferation of Ewing sarcoma cells and induced apoptosis, phenocopying pharmacologic inhibition of LDH. LDH inhibitors affected Ewing sarcoma cell viability both

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationEnzyme InhibitorsGlycolysisHumansL-Lactate DehydrogenaseMiceMice, SCIDSarcoma, EwingXenograft Model Antitumor AssaysAntineoplastic AgentsEnzyme InhibitorsL-Lactate Dehydrogenase

Identifiers

PMID31431459
PMCPMC6774872
OpenAlexW2969950932

What OpenQuestion holds

Textmetadata
LicenceTDM
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.