Evidence map›Paper›PMID 23574716›Full record

ArticleCell cycle (Georgetown, Tex.)2013

The significance of a Cripto-1 positive subpopulation of human melanoma cells exhibiting stem cell-like characteristics.

Luigi Strizzi, Naira V Margaryan, Alina Gilgur, Katharine M Hardy, Nicola Normanno, David S Salomon, Mary J C Hendrix

Open access · hybridAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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  14. Elevated expression of Cripto-1 correlates with poor prognosis in non-small cell lung cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  15. 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

7 authors at 4 institutions in 2 countries.

Luigi StrizziAnn & Robert H. Lurie Children's Hospital of Chicago Research Center, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. lstrizzi@luriechildrens.org
Naira V Margaryan
Alina Gilgur
Katharine M Hardy
Nicola Normanno
David S Salomon
Mary J C Hendrix
Northwestern University · USIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITLurie Children's Hospital · USNational Cancer Institute · US

Funding

Endothelial Transdifferentiation of Invasive Tumor CellsR37CA059702 · NCI · UNIVERSITY OF IOWA · PI HENDRIX, MARY J.C. · 2002 to 2011
$3.9M
Epigenetic Effect of the Microenvironment on Stem Cell Plasticity and FunctionR01CA121205 · NCI · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI HENDRIX, MARY J.C. · 2007 to 2011
$2.1M
Intramural NIH HHSNCI NIH HHS R01 CA121205NCI NIH HHS R01CA121205NCI NIH HHS R37 CA059702NCI NIH HHS R37CA59702
6 · The paper itself

Abstract

Cripto-1 (CR-1) protein function differs according to cellular or extracellular expression. In this study, we explore the significance of cell surface CR-1 expression in human melanoma cells. Cell surface CR-1-expressing human melanoma cells (CR1-CS+) were selected by fluorescence-activated cell sorting (FACS) and grown in vitro and in vivo in nude mice to study their growth characteristics. The CR1-CS+ melanoma cells were found to express increased levels of Oct4, MDR-1 and activated c-Src compared with cells lacking this subpopulation (CR1-CS-) or unsorted cells, used as control. CR1-CS+ show reduced proliferation rates and diminished spherical colony formation compared with control cells when cultured in vitro. Orthotopic injections of CR1-CS+ in nude mice formed slow growing tumors with histologic variability across different areas of the CR1-CS+ xenografts. CR-1-expressing cells from first generation CR1-CS+ tumors showed significantly increased tumor-forming rate and aggressiveness following subsequent transplants in nude mice. These data demonstrate that within a heterogeneous melanoma cell population there resides a slow proliferating, cell surface CR-1-expressing subpopulation capable of giving rise to a fast growing, aggressive progeny that may contribute to disease recurrence and progression.

Indexed as

AnimalsCarcinogenesisCell Line, TumorCell ProliferationCell SeparationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGPI-Linked ProteinsHumansIntercellular Signaling Peptides and ProteinsMelanomaMiceMice, NudeNeoplasm ProteinsNeoplastic Stem CellsGPI-Linked ProteinsIntercellular Signaling Peptides and ProteinsNeoplasm ProteinsTDGF1 protein, humanaggressivenessCripto-1melanomarecurrencetargettumorigenicity

Identifiers

PMID23574716
PMCPMC3674072
OpenAlexW2017539367

What OpenQuestion holds

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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.