Evidence map›Paper›PMID 31113844›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Arginine Starvation and Docetaxel Induce c-Myc-Driven hENT1 Surface Expression to Overcome Gemcitabine Resistance in ASS1-Negative Tumors.

Bethany C Prudner, Richa Rathore, Anthony M Robinson, Abigail Godec, Samuel F Chang, William G Hawkins, Angela C Hirbe, Brian A Van Tine

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Leiomyosarcoma Therapeutic Approaches and Future Directions.Hematology/oncology clinics of North America · 2025
    Review
  9. Article
  10. BCL-XL Protects ASS1-Deficient Cancers from Arginine Starvation-Induced Apoptosis.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Discovery and Targeting of a Noncanonical Mechanism of Sarcoma Resistance to ADI-PEG20 Mediated by the Microenvironment.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  16. Review
  17. Article
  18. Review
  19. Therapeutic advances in leiomyosarcoma.Frontiers in oncology · 2023
    Review
  20. 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

8 authors at 1 institution in 1 country.

Bethany C PrudnerDivision of Medical Oncology, Washington University in St. Louis, St. Louis, Missouri.ORCID 0000-0002-3522-9820
Richa RathoreDivision of Medical Oncology, Washington University in St. Louis, St. Louis, Missouri.ORCID 0000-0003-3708-8758
Anthony M RobinsonDivision of Medical Oncology, Washington University in St. Louis, St. Louis, Missouri.
Abigail GodecDivision of Medical Oncology, Washington University in St. Louis, St. Louis, Missouri.
Samuel F ChangDivision of Medical Oncology, Washington University in St. Louis, St. Louis, Missouri.ORCID 0000-0001-5083-3957
William G HawkinsDepartment of Surgery, Washington University School of Medicine, St. Louis, Missouri.
Angela C HirbeDivision of Medical Oncology, Washington University in St. Louis, St. Louis, Missouri.
Brian A Van TineDivision of Medical Oncology, Washington University in St. Louis, St. Louis, Missouri. bvantine@wustl.edu.ORCID 0000-0003-4572-6668
Washington University in St. Louis · US

Funding

USING ARGININE METABOLIC THERAPIES FOR SARCOMAR01CA227115 · NCI · WASHINGTON UNIVERSITY · PI VAN TINE, BRIAN ANDREW · 2019 to 2023
$1.8M
NCI NIH HHS R01 CA227115
6 · The paper itself

Abstract

purposeThe response to acute and long-term arginine starvation results in a conditional adaptive metabolic reprogramming that can be harnessed for therapeutic opportunities in ASS1-negative tumors. Here, we investigate the underlying biology of priming ASS1 EXPERIMENTAL

designASS1

resultsIn examining modulations within the pyrimidine pathway, we identified that the addition of DTX to cells treated with ADI-PEG20 resulted in translocation of stabilized c-Myc to the nucleus. This resulted in an increase of hENT1 cell-surface expression and rendered the cells susceptible to GEM.

conclusionsThe priming of tumors with ADI-PEG20 and DTX results in the stabilization of c-MYC potentiating the effect of GEM treatment via an increase in hENT1 expression. This finding is applicable to ASS1-deficient cancers that are currently treated with GEM.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsArginineArgininosuccinate SynthaseCell Line, TumorCell MembraneDeoxycytidineDisease Models, AnimalDocetaxelEquilibrative Nucleoside Transporter 1GemcitabineHumansMiceModels, BiologicalNeoplasmsProtein BindingArginineArgininosuccinate SynthaseDeoxycytidineDocetaxelEquilibrative Nucleoside Transporter 1GemcitabineProto-Oncogene Proteins c-mycSLC29A1 protein, human

Identifiers

PMID31113844
PMCPMC7357353
OpenAlexW2946452125

What OpenQuestion holds

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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.