Evidence map›Paper›PMID 28762556›Full record

ArticleMolecular carcinogenesis2017

NADPH oxidase 5 (NOX5)-induced reactive oxygen signaling modulates normoxic HIF-1α and p27

Smitha Antony, Guojian Jiang, Yongzhong Wu, Jennifer L Meitzler, Hala R Makhlouf, Diana C Haines, Donna Butcher, Dave S Hoon, Jiuping Ji, Yiping Zhang and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular carcinogenesis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Selective lysosomal HRSC advances · 2026
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  3. Redox processes in the treatment of advanced skin cancers.Clinical & experimental metastasis · 2026
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  4. Review
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  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Functional interactions between NADPH oxidase 5 and actin.Frontiers in cell and developmental biology · 2023
    Article
  14. Review
  15. AhR promotes phosphorylation of ARNT isoform 1 in human T cell malignancies as a switch for optimal AhR activity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Redox-Related Proteins in Melanoma Progression.Antioxidants (Basel, Switzerland) · 2022
    Article
  17. Article
  18. Overexpression ofGland surgery · 2022
    Article
  19. Review
  20. NOX Inhibitors: From Bench to Naxibs to Bedside.Handbook of experimental pharmacology · 2021
    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

17 authors at 3 institutions in 1 country.

Smitha AntonyDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.ORCID http://orcid.org/0000-0003-0718-1126
Guojian JiangDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
Yongzhong WuDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
Jennifer L MeitzlerDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
Hala R MakhloufDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
Diana C HainesPathology/Histotechnology Laboratory, Leidos Inc./Frederick National Laboratory for Cancer Research, National Cancer Institute, Frederick, Maryland.
Donna ButcherPathology/Histotechnology Laboratory, Leidos Inc./Frederick National Laboratory for Cancer Research, National Cancer Institute, Frederick, Maryland.
Dave S HoonDepartment of Molecular Oncology, John Wayne Cancer Institute, Santa Monica, California.
Jiuping JiDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
Yiping ZhangDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
Agnes JuhaszDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
Jiamo LuDevelopmental Therapeutics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
Han LiuDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
Iris DahanDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
Mariam KonateDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
Krishnendu K RoyDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
James H DoroshowDivision of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, Maryland.
National Cancer Institute · USLeidos (United States) · USSaint John's Health Center · US

Funding

NADPH Oxidase 1: A Novel Target for Colon Cancer TherapyZ01BC010677 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DOROSHOW, JAMES HALPERN · 2005 to 2008
$1.1M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z01 BC010677NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

NADPH oxidase 5 (NOX5) generated reactive oxygen species (ROS) have been implicated in signaling cascades that regulate cancer cell proliferation. To evaluate and validate NOX5 expression in human tumors, we screened a broad range of tissue microarrays (TMAs), and report substantial overexpression of NOX5 in malignant melanoma and cancers of the prostate, breast, and ovary. In human UACC-257 melanoma cells that possesses high levels of functional endogenous NOX5, overexpression of NOX5 resulted in enhanced cell growth, increased numbers of BrdU positive cells, and increased γ-H2AX levels. Additionally, NOX5-overexpressing (stable and inducible) UACC-257 cells demonstrated increased normoxic HIF-1α expression and decreased p27

Indexed as

Signal TransductionBlotting, WesternBreast NeoplasmsCell Line, TumorCell ProliferationCyclin-Dependent Kinase Inhibitor p27FemaleGlycogen Synthase Kinase 3 betaHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMelanomaNADPH Oxidase 5Ovarian NeoplasmsPhosphorylationProstatic NeoplasmsCDKN1B protein, humanCyclin-Dependent Kinase Inhibitor p27Glycogen Synthase Kinase 3 betaHypoxia-Inducible Factor 1, alpha SubunitNADPH Oxidase 5Proto-Oncogene Proteins c-aktReactive Oxygen SpeciesAkt/GSK3 signalingcell growthDNA damageNADPH oxidasereactive oxygen species (ROS)tumor microarray (TMA)

Identifiers

PMID28762556
PMCPMC5675809
OpenAlexW2741669988

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.