Evidence map›Paper›PMID 19767774›Full record

ArticleOncogene2009

'Loss of pigment epithelium-derived factor enables migration, invasion and metastatic spread of human melanoma'.

J L Orgaz, O Ladhani, K S Hoek, A Fernández-Barral, D Mihic, O Aguilera, E A Seftor, A Bernad, J L Rodríguez-Peralto, M J C Hendrix and 2 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

42 citing papers in PubMed, 73 citations in OpenAlex.

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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

12 authors at 5 institutions in 3 countries.

J L OrgazDepartment of Biochemistry, Universidad Autónoma de Madrid and Instituto de Investigaciones Biomédicas CSIC-UAM, Madrid, Spain.
O Ladhani
K S Hoek
A Fernández-Barral
D Mihic
O Aguilera
E A Seftor
A Bernad
J L Rodríguez-Peralto
M J C Hendrix
O V Volpert
B Jiménez
Northwestern University · USUniversidad Autónoma de Madrid · ESUniversity of Zurich · CHHospital Universitario 12 De Octubre · ESInstituto de Salud Carlos III · ES

Funding

CARCINOGENESIS TRAINING PROGRAMT32CA009560 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Kathleen Janee Green · 1986 to 2026
$8.4M
Endothelial Transdifferentiation of Invasive Tumor CellsR37CA059702 · NCI · UNIVERSITY OF IOWA · PI HENDRIX, MARY J.C. · 2002 to 2011
$3.9M
Regulation of angiogenic balance by thrombospondin-1.R01HL068033 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI VOLPERT, OLGA VALERY · 2001 to 2009
$2.6M
Maximization of anti-angiogenesis by thrombospondin-1R01HL077471 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI VOLPERT, OLGA VALERY · 2005 to 2008
$1.1M
CYTOKERATIN AND VIMENTIN EXPRESSION UNDERLIES METASTASISR01CA059702 · NCI · UNIVERSITY OF IOWA · PI HENDRIX, MARY J.C. · 1993 to 2000
$244k
NCI NIH HHS CA59702NCI NIH HHS R01 CA059702NCI NIH HHS R37 CA059702NCI NIH HHS T32 CA009560NCI NIH HHS T32CA009560NHLBI NIH HHS R01 HL068033NHLBI NIH HHS R01 HL077471NHLBI NIH HHS R01 HL68033
6 · The paper itself

Abstract

Pigment epithelium-derived factor (PEDF) is a multifunctional secreted glycoprotein that displays broad anti-tumor activity based on dual targeting of the tumor microenvironment (anti-angiogenic action) and the tumor cells (direct anti-tumor action). Here, we show that PEDF expression is high in melanocytes, but it is lost during malignant progression of human melanoma. Using a high-throughput analysis of the data from microarray studies of molecular profiling of human melanoma, we found that PEDF expression is lost in highly invasive melanomas. In paired cell lines established from the same lesion but representing the high and low extremes of malignant potential, abundant PEDF expression was restricted to the poorly aggressive counterparts. We used RNA interference to directly address the functional consequences of PEDF silencing. PEDF knockdown in poorly aggressive melanoma cell lines augmented migration, invasion and vasculogenic mimicry, which translated into an increased in vivo metastatic potential. PEDF interference also significantly enhanced the migratory and invasive capability of normal melanocytes and moderately increased their proliferative potential. Our results show that loss of PEDF enables melanoma cells to acquire an invasive phenotype and, therefore, modulation of this multifunctional factor could be critical for the malignant progression of human melanoma.

Indexed as

Cell MovementGene Expression Regulation, NeoplasticCell Line, TumorEye ProteinsGene Expression ProfilingHumansMelanomaNeoplasm InvasivenessNeoplasm MetastasisNeoplasm ProteinsNerve Growth FactorsOligonucleotide Array Sequence AnalysisPigment Epithelium-Derived FactorSerpinsEye ProteinsNeoplasm ProteinsNerve Growth FactorsPigment Epithelium-Derived FactorSerpins

Identifiers

PMID19767774
PMCPMC2873770
OpenAlexW2028994295

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.