Evidence map›Paper›PMID 19659570›Full record

ArticlePigment cell & melanoma research2009

NRG1 / ERBB3 signaling in melanocyte development and melanoma: inhibition of differentiation and promotion of proliferation.

Kristina Buac, Mai Xu, Julie Cronin, Ashani T Weeraratna, Stephen M Hewitt, William J Pavan

Open access · hybridAbstract read
In one paragraph

Article in Pigment cell & melanoma research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

47 citing papers in PubMed, 82 citations in OpenAlex.

  1. An Itch Receptor Drives Melanoma.bioRxiv : the preprint server for biology · 2026
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  5. Pannexin 1 crosstalk with the Hippo pathway in malignant melanoma.bioRxiv : the preprint server for biology · 2024
    Article
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  7. Genome-Wide Association Analysis Identifies theAnimals : an open access journal from MDPI · 2023
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  14. Review
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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

6 authors at 4 institutions in 1 country.

Kristina BuacGenetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Mai Xu
Julie Cronin
Ashani T Weeraratna
Stephen M Hewitt
William J Pavan
National Institute on Aging · USNational Institutes of Health · USGeorge Washington University · USNational Cancer Institute · US

Funding

Function genomic analysis of neural crest developmentZIAHG000136 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI PAVAN, WILLIAM J · 2009 to 2023
$13.6M
ANALYSIS OF DOMINANT MEGACOLON--ANOTHER MODEL FORHIRSCHSPRUNG DISEASEZIAHG000070 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI PAVAN, WILLIAM J · 2009 to 2023
$13.4M
Tissue Array Research ProgramZICBC010923 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HEWITT, STEPHEN · 2009 to 2014
$4.7M
Function genomic analysis of neural crest developmentZ01HG000136 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI PAVAN, WILLIAM J · 1999 to 2008
$2.3M
Role of Wnt Signaling in melanoma metastasis and melanocyte differentiationZIAAG000450 · NIA · NATIONAL INSTITUTE ON AGING · PI WEERARATNA, ASHANI · 2009 to 2010
$462k
Using gene expression profiles to elucidate mechanisms of melanoma progressionZIAAG000442 · NIA · NATIONAL INSTITUTE ON AGING · PI WEERARATNA, ASHANI · 2009 to 2010
$443k
Intramural NIH HHS Z01 HG000136
6 · The paper itself

Abstract

Neuregulin (NRG) signaling through the receptor tyrosine kinase, ERBB3, is required for embryonic development, and dysregulated signaling has been associated with cancer progression. Here, we show that NRG1/ERBB3 signaling inhibits melanocyte (MC) maturation and promotes undifferentiated, migratory and proliferative cellular characteristics. Embryonic analyses demonstrated that initial MC specification and distribution were not dependent on ERBB3 signaling. However NRG1/ERBB3 signaling was both necessary and sufficient to inhibit differentiation of later stages of MC development in culture. Analysis of tissue arrays of human melanoma samples suggests that ERBB3 signaling may also contribute to metastatic progression of melanoma as ERBB3 was phosphorylated in primary tumors compared with nevi or metastatic lesions. Neuregulin 1-treated MCs demonstrated increased proliferation and invasion and altered morphology concomitant with decreased levels of differentiation genes, increased levels of proliferation genes and altered levels of melanoma progression and metastases genes. ERBB3 activation in primary melanomas suggests that NRG1/ERBB3 signaling may contribute to the progression of melanoma from benign nevi to malignancies. We propose that targeting ERBB3 activation and downstream genes identified in this study may provide novel therapeutic interventions for malignant melanoma.

Indexed as

Cell ProliferationMelanomaAnimalsCell DifferentiationCell LineEmbryo, MammalianHumansMelaninsMelanocytesMembrane GlycoproteinsMiceMice, Inbred BALB CMice, Inbred C57BLMicrophthalmia-Associated Transcription FactorMonophenol MonooxygenaseNeoplasm InvasivenessMelaninsMembrane GlycoproteinsMicrophthalmia-Associated Transcription FactorMitf protein, mouseMonophenol MonooxygenaseNeuregulin-1OxidoreductasesReceptor, ErbB-3TYRP1 protein, human

Identifiers

PMID19659570
PMCPMC3023175
OpenAlexW2077812827

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.