Evidence map›Paper›PMID 36520504›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2023

Targeting Nitric Oxide: Say NO to Metastasis.

Tejaswini P Reddy, Sharon A Glynn, Timothy R Billiar, David A Wink, Jenny C Chang

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.7field-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

38 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. NO-PDT and chemotherapy: spatiotemporal control to achieve therapeutic synergy.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. NO/iNOS axis impact on glioma stem cells and temozolomide resistance.Journal of molecular medicine (Berlin, Germany) · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review
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

5 authors at 4 institutions in 2 countries.

Tejaswini P ReddyTexas A&M University Health Science Center, Bryan, Texas.ORCID 0000-0003-1806-1701
Sharon A GlynnProstate Cancer Institute, National University of Ireland Galway, Galway, Ireland.ORCID 0000-0003-1459-2580
Timothy R BilliarDepartment of Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.ORCID 0000-0002-2949-0811
David A WinkCancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute, National Institute of Health, Frederick, Maryland.ORCID 0000-0002-5652-7480
Jenny C ChangHouston Methodist Research Institute, Houston, Texas.ORCID 0000-0002-0890-9302
Houston Methodist · USFrederick National Laboratory for Cancer Research · USOllscoil na Gaillimhe – University of Galway · IEUniversity of Pittsburgh Medical Center · US

Funding

Nitric Oxide as a Modifier of Oxidative StressZIASC007281 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WINK, DAVID · 2009 to 2025
$8.1M
Dual targeting of PI3K and NOS pathways in Metaplastic BreastCancer (MBC)R01CA284315 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI JENNY C-N CHANG · 2023 to 2026
$2.6M
A phase II multi-center trial evaluating dual targeting of the PI3K/AKT and NOS pathways for treating metaplastic breast cancer (MpBC)U01CA268813 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI JENNY C-N CHANG, FUNDA MERIC-BERNSTAM · 2022 to 2026
$2.0M
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENCI NIH HHS R01 CA284315NCI NIH HHS U01 CA268813
6 · The paper itself

Abstract

Utilizing targeted therapies capable of reducing cancer metastasis, targeting chemoresistant and self-renewing cancer stem cells, and augmenting the efficacy of systemic chemo/radiotherapies is vital to minimize cancer-associated mortality. Targeting nitric oxide synthase (NOS), a protein within the tumor microenvironment, has gained interest as a promising therapeutic strategy to reduce metastatic capacity and augment the efficacy of chemo/radiotherapies in various solid malignancies. Our review highlights the influence of nitric oxide (NO) in tumor progression and cancer metastasis, as well as promising preclinical studies that evaluated NOS inhibitors as anticancer therapies. Lastly, we highlight the prospects and outstanding challenges of using NOS inhibitors in the clinical setting.

Indexed as

NeoplasmsNitric OxideHumansNitric Oxide SynthaseNitric Oxide Synthase Type IITumor MicroenvironmentNitric OxideNitric Oxide SynthaseNitric Oxide Synthase Type II

Identifiers

PMID36520504
PMCPMC10183809
OpenAlexW4311575467

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.