Evidence map›Paper›PMID 20018867›Full record

ArticleThe Journal of biological chemistry2010

Reactive oxygen generated by NADPH oxidase 1 (Nox1) contributes to cell invasion by regulating matrix metalloprotease-9 production and cell migration.

Masahiro Shinohara, Yoshifumi Adachi, Junji Mitsushita, Mitsuhiro Kuwabara, Atsushi Nagasawa, Saori Harada, Shuichi Furuta, Yugen Zhang, Kajla Seheli, Hitoshi Miyazaki and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

57 citing papers in PubMed, 104 citations in OpenAlex.

  1. The Pro-Metastatic Roles of ROS.Antioxidants (Basel, Switzerland) · 2026
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  19. Senescence in Vascular Smooth Muscle Cells and Atherosclerosis.Frontiers in cardiovascular medicine · 2022
    Review
  20. 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

11 authors at 2 institutions in 1 country.

Masahiro ShinoharaDepartment of Molecular Biology and Biochemistry, Shinshu University Graduate School of Medicine, Matsumoto, Nagano 390-8621, Japan.
Yoshifumi Adachi
Junji Mitsushita
Mitsuhiro Kuwabara
Atsushi Nagasawa
Saori Harada
Shuichi Furuta
Yugen Zhang
Kajla Seheli
Hitoshi Miyazaki
Tohru Kamata
Shinshu University · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A mediating role of the reactive oxygen species-generating enzyme Nox1 has been suggested for Ras oncogene transformation phenotypes including anchorage-independent cell growth, augmented angiogenesis, and tumorigenesis. However, little is known about whether Nox1 signaling regulates cell invasiveness. Here, we report that the cell invasion activity was augmented in K-Ras-transformed normal rat kidney cells and attenuated by transfection of Nox1 small interference RNAs (siRNAs) into the cells. Diphenyleneiodonium (DPI) or Nox1 siRNAs blocked up-regulation of matrix metalloprotease-9 at both protein and mRNA levels in K-Ras-transformed normal rat kidney cells. Furthermore, DPI and Nox1 siRNAs inhibited the activation of IKKalpha kinase and the degradation of IkappaB alpha, suppressing the NFkappaB-dependent matrix metalloprotease-9 promoter activity. Additionally, epidermal growth factor-stimulated migration of CaCO-2 cells was abolished by DPI and Nox1 siRNAs, indicating the requirement of Nox1 activity for the motogenic effect of epidermal growth factor. This Nox1 action was mediated by down-regulation of the Rho activity through the low molecular weight protein-tyrosine phosphatase-p190RhoGAP-dependent mechanism. Taken together, our findings define a mediating role of Nox1-generated reactive oxygen species in cell invasion processes, most notably metalloprotease production and cell motile activity.

Indexed as

AnimalsAntioxidantsCaco-2 CellsCell LineCell MovementEpidermal Growth FactorHumansI-kappa B KinaseImmunoblottingImmunoprecipitationMatrix Metalloproteinase 2Matrix Metalloproteinase 9NADH, NADPH OxidoreductasesNADPH Oxidase 1Onium CompoundsPromoter Regions, GeneticAntioxidantsdiphenyleneiodoniumEpidermal Growth FactorI-kappa B KinaseMatrix Metalloproteinase 2Matrix Metalloproteinase 9NADH, NADPH OxidoreductasesNADPH Oxidase 1NOX1 protein, ratOnium CompoundsProto-Oncogene ProteinsReactive Oxygen Speciesrho GTP-Binding ProteinsVitamin E

Identifiers

PMID20018867
PMCPMC2836054
OpenAlexW2057893902

What OpenQuestion holds

Textmetadata
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.