Evidence map›Paper›PMID 31167399›Full record

ReviewCancers2019

The Pleiotropic Effects of Glutamine Metabolism in Cancer.

Alex J Bott, Sara Maimouni, Wei-Xing Zong

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing 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

71 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Dichloroacetate for Cancer Treatment: Some Facts and Many Doubts.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

11 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

3 authors at 2 institutions in 1 country.

Alex J BottDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.ORCID 0000-0003-2273-8922
Sara MaimouniDepartment of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers Cancer Institute of New Jersey, Rutgers-The State University of New Jersey, 164 Frelinghuysen Rd, Piscataway, NJ 08854, USA.ORCID 0000-0002-6085-0766
Wei-Xing ZongDepartment of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers Cancer Institute of New Jersey, Rutgers-The State University of New Jersey, 164 Frelinghuysen Rd, Piscataway, NJ 08854, USA. zongwx@rutgers.edu.ORCID 0000-0002-3129-8220
Rutgers, The State University of New Jersey · USUniversity of Utah · US

Funding

Protein and redox homeostasis in cancer development and therapyR01CA129536 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI ZONG, WEI-XING · 2008 to 2022
$4.8M
Glutamine synthetase in cancer cell metabolism and oncogenesisR01CA224550 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI Wei-Xing Zong · 2018 to 2026
$4.7M
PI3 kinase PIK3CB (p110beta) in membrane trafficking and metabolismR01CA232246 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI ZONG, WEI-XING · 2018 to 2022
$1.8M
Identifying epigenetic targets of c-myc oncogeneR21CA205172 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI WU, SONG, ZONG, WEI-XING · 2016 to 2017
$382k
Myc-induced expression of glutamine synthetaseK00CA212445 · NCI · UNIVERSITY OF UTAH · PI BOTT, ALEX · 2018 to 2021
$367k
Myc-induced expression of glutamine synthetaseF99CA212445 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI BOTT, ALEX · 2016 to 2017
$77k
NCI NIH HHS F99 CA212445NCI NIH HHS K00 CA212445NCI NIH HHS R01 CA129536NCI NIH HHS R01 CA224550NCI NIH HHS R01CA224550, K00CA212445NCI NIH HHS R01 CA232246NCI NIH HHS R21 CA205172
6 · The paper itself

Abstract

Metabolic programs are known to be altered in cancers arising from various tissues. Malignant transformation can alter signaling pathways related to metabolism and increase the demand for both energy and biomass for the proliferating cancerous cells. This scenario is further complexed by the crosstalk between transformed cells and the microenvironment. One of the most common metabolic alterations, which occurs in many tissues and in the context of multiple oncogenic drivers, is the increased demand for the amino acid glutamine. Many studies have attributed this increased demand for glutamine to the carbon backbone and its role in the tricarboxylic acid (TCA) cycle anaplerosis. However, an increasing number of studies are now emphasizing the importance of glutamine functioning as a proteogenic building block, a nitrogen donor and carrier, an exchanger for import of other amino acids, and a signaling molecule. Herein, we highlight the recent literature on glutamine's versatile role in cancer, with a focus on nitrogen metabolism, and therapeutic implications of glutamine metabolism in cancer.

Indexed as

cancerglutamateglutamate ammonia ligase (GLUL)glutaminase (GLS)glutamineglutamine synthetase (GS)glutaminolysismetabolism

Identifiers

PMID31167399
PMCPMC6627534
OpenAlexW2948707395

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.