Evidence map›Paper›PMID 28925403›Full record

ArticleOncogene2018

A slow-cycling subpopulation of melanoma cells with highly invasive properties.

M Perego, M Maurer, J X Wang, S Shaffer, A C Müller, K Parapatics, L Li, D Hristova, S Shin, F Keeney and 8 more

Abstract read
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
–field-weighted citation impact
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

54 citing papers in PubMed.

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  9. Pseudoassembly of k-mers.bioRxiv : the preprint server for biology · 2025
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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

18 authors.

M PeregoMelanoma Research Center, The Wistar Institute, Philadelphia, PA, USA.
M MaurerDivision of Immunology, Allergy and Infectious Diseases, Medical University of Vienna, Vienna, Austria.
J X WangMelanoma Research Center, The Wistar Institute, Philadelphia, PA, USA.
S ShafferDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
A C MüllerCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
K ParapaticsCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
L LiMelanoma Research Center, The Wistar Institute, Philadelphia, PA, USA.
D HristovaMelanoma Research Center, The Wistar Institute, Philadelphia, PA, USA.
S ShinMelanoma Research Center, The Wistar Institute, Philadelphia, PA, USA.
F KeeneyMelanoma Research Center, The Wistar Institute, Philadelphia, PA, USA.
S LiuDepartment of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
X XuDepartment of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
A RajDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
J K JensenDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.
K L BennettCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
S N WagnerDivision of Immunology, Allergy and Infectious Diseases, Medical University of Vienna, Vienna, Austria.
R SomasundaramMelanoma Research Center, The Wistar Institute, Philadelphia, PA, USA.
M HerlynMelanoma Research Center, The Wistar Institute, Philadelphia, PA, USA.

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Targeting the MAP and PI3 Kinase Pathways in MelanomaP01CA114046 · NCI · WISTAR INSTITUTE · PI MURPHY, MAUREEN E. · 2008 to 2023
$37.1M
TUMOR DEVELOPMENT AND PROGRESSION IN HUMAN MELANOCYTESP01CA025874 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 1985 to 2015
$19.0M
Targeted Combination Therapy for MelanomaP50CA174523 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2014 to 2018
$11.1M
CELL/CELL COMMUNICATION DURING MELANOMA PROGRESSIONR01CA076674 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 1998 to 2015
$4.0M
METASTATIS: BIOLOGICAL PHENOTYPE AND MODELS FOR THERAPYR01CA047159 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 1989 to 2015
$3.9M
The role of genetic susceptibility in melanoma developmentR01CA182890 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2014 to 2018
$2.1M
Purchase a Beckman Coulter MoFlo Astrios Flow CytometerS10OD017998 · OD · WISTAR INSTITUTE · PI MONTANER, LUIS J · 2014 to 2014
$595k
NCI NIH HHS P01 CA025874NCI NIH HHS P01 CA114046NCI NIH HHS P30 CA010815NCI NIH HHS P50 CA174523NCI NIH HHS R01 CA047159NCI NIH HHS R01 CA076674NCI NIH HHS R01 CA182890NIH HHS S10 OD017998
6 · The paper itself

Abstract

Melanoma is a heterogeneous tumor with different subpopulations showing different proliferation rates. Slow-cycling cells were previously identified in melanoma, but not fully biologically characterized. Using the label-retention method, we identified a subpopulation of slow-cycling cells, defined as label-retaining cells (LRC), with strong invasive properties. We demonstrate through live imaging that LRC are leaving the primary tumor mass at a very early stage and disseminate to peripheral organs. Through global proteome analyses, we identified the secreted protein SerpinE2/protease nexin-1 as causative for the highly invasive potential of LRC in melanomas.

Indexed as

Cell CycleAnimalsCell Line, TumorCell SeparationFlow CytometryHumansMelanocytesMelanomaMiceNeoplasm InvasivenessProteomicsSerpin E2SkinSkin NeoplasmsXenograft Model Antitumor AssaysSerpin E2SERPINE2 protein, human

Identifiers

PMID28925403
PMCPMC5799768

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.