Evidence map›Paper›PMID 24468749›Full record

ArticleThe Journal of investigative dermatology2014

Role of CRD-BP in the growth of human basal cell carcinoma cells.

Felicite K Noubissi, TaeWon Kim, Tisha N Kawahara, William D Aughenbaugh, Eric Berg, B Jack Longley, Mohammad Athar, Vladimir S Spiegelman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

31 citing papers in PubMed, 46 citations in OpenAlex.

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  17. Cross-Talk between Wnt and Hh Signaling Pathways in the Pathology of Basal Cell Carcinoma.International journal of environmental research and public health · 2018
    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

8 authors at 3 institutions in 1 country.

Felicite K NoubissiDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA. Electronic address: fnoubiss@umn.edu.
TaeWon KimDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA; Molecular and Environmental Toxicology Center Graduate Program, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Tisha N KawaharaDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA; Carbone Comprehensive Cancer Center, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
William D AughenbaughDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA; Carbone Comprehensive Cancer Center, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Eric BergDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA; Carbone Comprehensive Cancer Center, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
B Jack LongleyDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA; Carbone Comprehensive Cancer Center, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Mohammad AtharDepartment of Dermatology, University of Alabama, Birmingham, Alabama, USA.
Vladimir S SpiegelmanDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA; Molecular and Environmental Toxicology Center Graduate Program, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA; Carbone Comprehensive Cancer Center, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
University of Wisconsin–Madison · USUniversity of Wisconsin Carbone Cancer Center · USUniversity of Alabama at Birmingham · US

Funding

RNA-binding protein CRD-BP in melanocyte biologyR01AR063361 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI SPIEGELMAN, VLADIMIR S. · 2013 to 2017
$1.6M
Inhibiting Multiple Molecular Targets for Preventing Non-Melanoma Skin CancerR01CA138998 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ATHAR, MOHAMMAD · 2011 to 2015
$1.5M
The Role of CRD-BP-regulated mRNA Stability in Colorectal CancersR01CA121851 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SPIEGELMAN, VLADIMIR S. · 2007 to 2011
$1.4M
Role of CRD-BP in Basal Cell Carcinoma DevelopmentR21CA153102 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI NOUBISSI, FELICITE K · 2010 to 2011
$350k
NCI NIH HHS CA121851NCI NIH HHS CA153102NCI NIH HHS R01 CA121851NCI NIH HHS R01 CA138998NCI NIH HHS R21 CA153102NIAMS NIH HHS AR063361NIAMS NIH HHS R01 AR063361
6 · The paper itself

Abstract

Although the number of new cases of basal cell carcinoma (BCC) has increased rapidly in the last few decades, the molecular basis of its pathogenesis is not completely understood. Activation of the Hedgehog (Hh) signaling pathway has been shown to be a key factor driving the development of BCC. The Wnt/β-catenin signaling pathway was also shown to be activated in BCCs and to perhaps modulate the activity of the Hh pathway. We have previously identified a mechanism by which Wnt signaling regulates the transcriptional outcome of the Hh signaling pathway. We demonstrated that coding region determinant-binding protein (CRD-BP), a direct target of the Wnt/β-catenin signaling, binds to GLI1 mRNA, stabilizes it, and consequently upregulates its levels (mRNA and protein) and activities. We hypothesized that Wnt-induced and CRD-BP-dependent regulation of GLI1 expression and activities is important for the development of BCC. In this study, we show that CRD-BP is overexpressed in BCC and that its expression positively correlates with the activation of both Wnt and Hh signaling pathways. We also describe the generation and characterization of a human BCC cell line. This cell line was utilized to demonstrate the importance of CRD-BP-dependent regulation of GLI1 expression and activities in the development of BCC.

Indexed as

Wnt Signaling PathwayAnimalsApoptosisBasal Cell CarcinomaCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHedgehog ProteinsHumansKeratinocytesMaleMiceMice, NudeNeoplasm InvasivenessRNA-Binding ProteinsRNA, MessengerCRD-BP protein, mouseGLI1 protein, humanHedgehog ProteinsIGF2BP1 protein, humanRNA-Binding ProteinsRNA, MessengerTelomeraseTERT protein, humanTranscription FactorsZinc Finger Protein GLI1

Identifiers

PMID24468749
PMCPMC4041658
OpenAlexW1987774694

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.