Evidence map›Paper›PMID 22033009›Full record

ReviewFree radical biology & medicine2012

Redox signaling at invasive microdomains in cancer cells.

Begoña Díaz, Sara A Courtneidge

Open access · greenAbstract readReview
In one paragraph

Review in Free radical biology & medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  7. Review
  8. Paradoxical roles of dual oxidases in cancer biology.Free radical biology & medicine · 2017
    Review
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  11. Article
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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.

Begoña DíazCancer Center, Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA.
Sara A Courtneidge
Sanford Burnham Prebys Medical Discovery Institute · US

Funding

Reactive Oxygen Species and Cancer Cell InvasionR01CA129686 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI COURTNEIDGE, SARA A · 2007 to 2011
$1.8M
Generation and utility of NADPH oxidase inhibitorsR01CA153065 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI COURTNEIDGE, SARA A · 2010 to 2012
$1.2M
NCI NIH HHS R01 CA129686NCI NIH HHS R01 CA153065
6 · The paper itself

Abstract

Redox signaling contributes to the regulation of cancer cell proliferation, survival, and invasion and participates in the adaptation of cancer cells to their microenvironment. NADPH oxidases are important mediators of redox signaling in normal and cancer cells. Redox signal specificity in normal cells is in part achieved by targeting enzymes that generate reactive oxygen species to specific subcellular microdomains such as focal adhesions, dorsal ruffles, lipid rafts, or caveolae. In a similar fashion, redox signal specificity during cancer cell invasion can be regulated by targeting reactive oxygen generation to invasive microdomains such as invadopodia. Here we summarize recent advances in the understanding of the redox signaling processes that control the cancer cell proinvasive program by modulating cell adhesion, migration, and proteolysis as well as the interaction of cancer cells with the tumor microenvironment. We focus on redox signaling events mediated by invadopodia NADPH oxidase complexes and their contribution to cancer cell invasion.

Indexed as

Signal TransductionAnimalsCell AdhesionCell MovementCell Surface ExtensionsHumansMembrane MicrodomainsNADPH OxidasesNeoplasm InvasivenessNeoplasmsOxidation-ReductionReactive Oxygen SpeciesTumor MicroenvironmentNADPH OxidasesReactive Oxygen Species

Identifiers

PMID22033009
PMCPMC3272498
OpenAlexW2057340727

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.