Evidence map›Paper›PMID 17147806›Full record

ArticleBMC genomics2006

Ethanol sensitivity: a central role for CREB transcription regulation in the cerebellum.

George K Acquaah-Mensah, Vikas Misra, Shyam Biswal

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Epigenetics-beyond the genome in alcoholism.Alcohol research : current reviews · 2012
    Article
  9. Implication of the purinergic system in alcohol use disorders.Alcoholism, clinical and experimental research · 2011
    Review
  10. Neuroscience of alcoholism: molecular and cellular mechanisms.Cellular and molecular life sciences : CMLS · 2010
    Review
  11. 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

3 authors at 2 institutions in 1 country.

George K Acquaah-MensahDepartment of Pharmaceutical Sciences, School of Pharmacy-Worcester, Massachusetts College of Pharmacy and Health Sciences, 19 Foster Street, Worcester, MA 01608-1715, USA. george.acquaah-mensah@mcphs.edu
Vikas Misra
Shyam Biswal
Johns Hopkins University · USMCPHS University · US

Funding

TARGETING EARLY CHANGES FOR NEW SCREENING STRATEGIESP50CA058184 · NCI · JOHNS HOPKINS UNIVERSITY · PI BISWAL, SHYAM · 1992 to 2013
$30.5M
Modifier Role of Nrf2 in Lung Injury and EmphysemaR01HL081205 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BISWAL, SHYAM · 2005 to 2009
$2.0M
NCI NIH HHS P50 CA058184NHLBI NIH HHS HL081205NHLBI NIH HHS R01 HL081205NIEHS NIH HHS P30 ES 038819
6 · The paper itself

Abstract

backgroundLowered sensitivity to the effects of ethanol increases the risk of developing alcoholism. Inbred mouse strains have been useful for the study of the genetic basis of various drug addiction-related phenotypes. Inbred Long-Sleep (ILS) and Inbred Short-Sleep (ISS) mice differentially express a number of genes thought to be implicated in sensitivity to the effects of ethanol. Concomitantly, there is evidence for a mediating role of cAMP/PKA/CREB signalling in aspects of alcoholism modelled in animals. In this report, the extent to which CREB signalling impacts the differential expression of genes in ILS and ISS mouse cerebella is examined.

resultsA training dataset for Machine Learning (ML) and Exploratory Data Analyses (EDA) was generated from promoter region sequences of a set of genes known to be targets of CREB transcription regulation and a set of genes whose transcription regulations are potentially CREB-independent. For each promoter sequence, a vector of size 132, with elements characterizing nucleotide composition features was generated. Genes whose expressions have been previously determined to be increased in ILS or ISS cerebella were identified, and their CREB regulation status predicted using the ML scheme C4.5. The C4.5 learning scheme was used because, of four ML schemes evaluated, it had the lowest predicted error rate. On an independent evaluation set of 21 genes of known CREB regulation status, C4.5 correctly classified 81% of instances with F-measures of 0.87 and 0.67 respectively for the CREB-regulated and CREB-independent classes. Additionally, six out of eight genes previously determined by two independent microarray platforms to be up-regulated in the ILS or ISS cerebellum were predicted by C4.5 to be transcriptionally regulated by CREB. Furthermore, 64% and 52% of a cross-section of other up-regulated cerebellar genes in ILS and ISS mice, respectively, were deemed to be CREB-regulated.

conclusionThese observations collectively suggest that ethanol sensitivity, as it relates to the cerebellum, may be associated with CREB transcription activity.

Indexed as

Transcription, GeneticAlcoholismAnimalsArtificial IntelligenceBehavior, AnimalCerebellumCyclic AMP Response Element-Binding ProteinEthanolMiceNF-E2-Related Factor 2PhenotypeSleepCyclic AMP Response Element-Binding ProteinEthanolNF-E2-Related Factor 2

Identifiers

PMID17147806
PMCPMC1698922
OpenAlexW2123751082

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.