Evidence map›Paper›PMID 29179997›Full record

ArticleCancer letters2018

Elevated cyclic AMP levels promote BRAF

Carlos I Rodríguez, Edgardo Castro-Pérez, B Jack Longley, Vijayasaradhi Setaluri

Abstract read
In one paragraph

Article in Cancer letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Cyclic AMP-regulatory element-binding protein: a novel UV-targeted transcription factor in skin cancer.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2024
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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

4 authors at 2 institutions in 1 country.

Carlos I RodríguezMolecular and Environmental Toxicology Center, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53706, USA; Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA. Electronic address: carlos.rodrigueznegron@ucsf.edu.
Edgardo Castro-PérezDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA.
B Jack LongleyDepartment of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA.
Vijayasaradhi SetaluriMolecular and Environmental Toxicology Center, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53706, USA; Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI 53705, USA. Electronic address: setaluri@wisc.edu.
University of Wisconsin–Madison · USWilliam S. Middleton Memorial Veterans Hospital · US

Funding

Molecular & Environmental Toxicology Pre-& Postdoctoral Training ProgramT32ES007015 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI CHRISTOPHER A BRADFIELD · 1985 to 2026
$11.5M
Skin Diseases Research Center at the University of WisconsinP30AR066524 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI LONGLEY, B JACK · 2014 to 2018
$2.6M
Prognostic Significance of Neuronal Differentiation of Cutaneous MelanomaR21CA125091 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SETALURI, VIJAYASARADHI · 2008 to 2009
$364k
Role of Notch Signaling in Melanoma Transdifferentiation and Tumor ProgressionI01BX002623 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI SETALURI, VIJAYASARADHI · 2015 to 2019
–
BLRD VA I01 BX002623NCI NIH HHS R21 CA125091NIAMS NIH HHS P30 AR066524NIEHS NIH HHS T32 ES007015
6 · The paper itself

Abstract

Melanocyte development and differentiation are regulated by cAMP, which is produced by the adenylate cyclase (AC) enzyme upon activation of the melanocortin-1-receptor (MC1R). Individuals carrying single amino acid substitution variants of MC1R have impaired cAMP signaling and higher risk of melanoma. However, the contribution of AC to this risk is not clear. Downstream of AC, the phosphorylated transcription factor, cyclic AMP Responsive Element Binding Protein (pCREB), which is activated by protein kinase A, regulates the expression of several genes including the melanocyte master regulator MITF. The roles of AC and CREB in melanoma development and growth are not well understood. Here, we investigated the effect of topical application of AC inhibitor on Braf

Indexed as

AdenineAdenylyl Cyclase InhibitorsAdultAgedAnimalsCell Line, TumorCyclic AMPCyclic AMP Response Element-Binding ProteinDisease ProgressionFemaleHumansKaplan-Meier EstimateMaleMelanomaMice, KnockoutMice, Transgenic9-(tetrahydro-2-furyl)-adenineAdenineAdenylyl Cyclase InhibitorsCyclic AMPCyclic AMP Response Element-Binding ProteinProto-Oncogene Proteins B-rafPTEN PhosphohydrolaseAdenylate cyclase (AC)BRAF/PTEN melanomaCREBCyclic AMP (cAMP)Melanoma progressionMelanoma tissue microarray

Identifiers

PMID29179997
PMCPMC5743623
OpenAlexW2768771874

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.