Evidence map›Paper›PMID 20890299›Full record

ArticleOncogene2011

DUSP1/MKP1 promotes angiogenesis, invasion and metastasis in non-small-cell lung cancer.

V Moncho-Amor, I Ibañez de Cáceres, E Bandres, B Martínez-Poveda, J L Orgaz, I Sánchez-Pérez, S Zazo, A Rovira, J Albanell, B Jiménez and 4 more

Abstract read
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In one paragraph

Article in Oncogene, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

62 citing papers in PubMed, 120 citations in OpenAlex.

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2 more citing papers are in PubMed but not listed here.

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

14 authors at 8 institutions in 1 country.

V Moncho-AmorInstituto de Investigaciones Biomedicas CSIC/UAM, CIBER de Enfermedades Raras (CIBERER), IdiPAZ, Madrid, Spain.
I Ibañez de Cáceres
E Bandres
B Martínez-Poveda
J L Orgaz
I Sánchez-Pérez
S Zazo
A Rovira
J Albanell
B Jiménez
F Rojo
C Belda-Iniesta
J García-Foncillas
R Perona
Instituto de Investigaciones Biomédicas Sols-Morreale · ESCentre for Biomedical Network Research on Rare Diseases · ESUniversidad de Navarra · ESUniversitat Autònoma de Barcelona · ESHospital Del Mar · ESHospital Universitario Fundación Jiménez Díaz · ESHospital Universitario La Paz · ESInstituto de Investigación de Enfermedades Raras · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DUSP1/MKP1 is a dual-specific phosphatase that regulates MAPKs activity, with an increasingly recognized role in tumor biology. To understand more about the involvement of DUSP1 in lung cancer, we performed gene expression analyses of parental and DUSP1-interfered H460 non-small-cell lung cancer (NSCLC) cells. Downregulation of DUSP1 induced changes in the expression levels of genes involved in specific biological pathways, including angiogenesis, MAP kinase phosphatase activity, cell-cell signaling, growth factor and tyrosine-kinase receptor activity. Changes in the expression of some of these genes were due to modulation of c-Jun-N-terminal kinase and/or p38 activity by DUSP1. Complementary functional assays were performed to focus on the implication of DUSP1 in angiogenesis and metastasis. In H460 cells, interference of DUSP1 resulted in a diminished capacity to invade through Matrigel, to grow tumors in nude mice and also to induce metastasis through tail-vein injection. Furthermore, the angiogenic potential of H460 cells was also impaired, correlating with a decrease in VEGFC production and indicating that DUSP1 could be required to induce angiogenesis. Finally, we studied whether a similar relationship occurred in patients. In human NSCLC specimens, DUSP1 was mainly expressed in those tumor cells close to CD31 vascular structures and a statistically significant correlation was found between VEGFC and DUSP1 expression. Overall, these results provide evidence for a role of DUSP1 in angiogenesis, invasion and metastasis in NSCLC.

Indexed as

AnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorDown-RegulationDual Specificity Phosphatase 1Gene Expression ProfilingHumansLung NeoplasmsMiceMice, NudeNeoplasm InvasivenessNeoplasm MetastasisNeovascularization, PathologicPlatelet Endothelial Cell Adhesion Molecule-1RNA, Small InterferingSignal TransductionDual Specificity Phosphatase 1DUSP1 protein, humanPlatelet Endothelial Cell Adhesion Molecule-1RNA, Small InterferingVascular Endothelial Growth Factor CVEGFC protein, human

Identifiers

PMID20890299
OpenAlexW2075995473

What OpenQuestion holds

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Registered trials

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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.