Evidence map›Paper›PMID 23590833›Full record

ReviewCurrent molecular medicine2013

iNOS: a potential therapeutic target for malignant glioma.

A Jahani-Asl, A Bonni

Open access · greenAbstract readReview
In one paragraph

Review in Current molecular medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

34 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. The Triple Crown: NO, CO, and HPharmacology & therapeutics · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Targeting Immunometabolism in Glioblastoma.Frontiers in oncology · 2021
    Review
  10. Review
  11. Article
  12. Sirt1-Overexpressing Mesenchymal Stem Cells Drive the Anti-tumor Effect through Their Pro-inflammatory Capacity.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. The dichotomous role of HBiochemical pharmacology · 2018
    Review
  20. NO and COX2: Dual targeting for aggressive cancers.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

2 authors at 1 institution in 1 country.

A Jahani-AslDepartment of Anatomy and Neurobiology, Washington University School of Medicine, Campus Box 8108, 660 South Euclid Ave, St Louis, MO 63110, USA.
A Bonni
Washington University in St. Louis · US

Funding

STAT3 REGULATION OF GLIOBLASTOMA PATHOGENESISR01NS064007 · NINDS · WASHINGTON UNIVERSITY · PI BONNI, AZAD · 2009 to 2013
$1.7M
NINDS NIH HHS NS064007NINDS NIH HHS R01 NS064007
6 · The paper itself

Abstract

Glioblastoma is the most aggressive adult primary brain tumor. Although progress has been made in understanding the molecular mechanisms underlying these tumors, current treatments are ineffective. Recent studies have identified iNOS as a critical regulator of glial transformation downstream of EGFRvIII/STAT3 signaling, a key oncogenic pathway in glioblastoma. STAT3 directly binds the promoter of the iNOS gene and thereby stimulates its expression. Importantly, inhibition of iNOS by genetic and pharmacological approaches impedes glial cell proliferation, invasiveness, and tumor growth in vivo. iNOS expression is also elevated in a population of human brain tumor stem cells (BTSCs), and iNOS is required for BTSC proliferation and tumorigenesis. Together, these findings suggest that development of iNOS-targeted therapies may prove valuable in the treatment of glioblastoma. Here, we review our current understanding of iNOS signaling in the regulation of glioblastoma pathogenesis and the potential mechanisms by which iNOS inhibition might suppress the malignant behavior of these devastating tumors.

Indexed as

AnimalsAntineoplastic AgentsBrain NeoplasmsErbB ReceptorsGliomaHumansMolecular Targeted TherapyNitric Oxide Synthase Type IISignal TransductionSTAT3 Transcription FactorAntineoplastic Agentsepidermal growth factor receptor VIIIErbB ReceptorsNitric Oxide Synthase Type IISTAT3 Transcription Factor

Identifiers

PMID23590833
PMCPMC4266467
OpenAlexW2067832229

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.