Evidence map›Paper›PMID 23686612›Full record

ReviewCell biochemistry and biophysics2013

Regulating the ubiquitin/proteasome pathway via cAMP-signaling: neuroprotective potential.

He Huang, Hu Wang, Maria E Figueiredo-Pereira

Abstract readReview
In one paragraph

Review in Cell biochemistry and biophysics, 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
1.6field-weighted citation impact, top 17% 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, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. S100A8 Protects Human Primary Alveolar Type II Cells against Injury and Emphysema.American journal of respiratory cell and molecular biology · 2019
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

3 authors at 2 institutions in 1 country.

He HuangDepartment of Biological Sciences, Hunter College and Graduate Center, City University of New York, 695 Park Avenue, New York, NY 10065, USA.
Hu Wang
Maria E Figueiredo-Pereira
The Graduate Center, CUNY · USHunter College · US

Funding

WILD TYPE &MUTANT P53 INTERACTIONS WITH HIV LTR DNAG12RR003037 · NCRR · HUNTER COLLEGE · PI STEIPER, MICHAEL E · 1985 to 2011
$27.6M
SNRP AT HUNTER COLLEGEU54NS041073 · NINDS · HUNTER COLLEGE · PI FILBIN, MARIE T. · 2000 to 2010
$16.4M
Basic and Translational Research Center for Reducing Health DisparitiesG12MD007599 · NIMHD · HUNTER COLLEGE · PI ANGULO, JESUS A · 2012 to 2017
$14.6M
Inflammation and the Ubiquitin/Proteasome Pathway in Neurodegeneration.R01AG028847 · NIA · HUNTER COLLEGE · PI FIGUEIREDO-PEREIRA, MARIA EMILIA · 2009 to 2010
$782k
NCRR NIH HHS G12 RR003037NCRR NIH HHS RR003037NIA NIH HHS R01 AG028847NIMHD NIH HHS G12 MD007599NINDS NIH HHS NS041073NINDS NIH HHS U54 NS041073
6 · The paper itself

Abstract

The cAMP-signaling pathway has been under intensive investigation for decades. It is a wonder that such a small simple molecule like cAMP can modulate a vast number of diverse processes in different types of cells. The ubiquitous involvement of cAMP-signaling in a variety of cellular events requires tight spatial and temporal control of its generation, propagation, compartmentalization, and elimination. Among the various steps of the cAMP-signaling pathway, G-protein-coupled receptors, adenylate cyclases, phosphodiesterases, the two major cAMP targets, i.e., protein kinase A and exchange protein activated by cAMP, as well as the A-kinase anchoring proteins, are potential targets for drug development. Herein we review the recent progress on the regulation and manipulation of different steps of the cAMP-signaling pathway. We end by focusing on the emerging role of cAMP-signaling in modulating protein degradation via the ubiquitin/proteasome pathway. New discoveries on the regulation of the ubiquitin/proteasome pathway by cAMP-signaling support the development of new therapeutic approaches to prevent proteotoxicity in chronic neurodegenerative disorders and other human disease conditions associated with impaired protein turnover by the ubiquitin/proteasome pathway and the accumulation of ubiquitin-protein aggregates.

Indexed as

Signal TransductionColforsinCyclic AMPHumansNeurodegenerative DiseasesPhosphodiesterase InhibitorsPituitary Adenylate Cyclase-Activating PolypeptideProteasome Endopeptidase ComplexUbiquitinVasodilator AgentsColforsinCyclic AMPPhosphodiesterase InhibitorsPituitary Adenylate Cyclase-Activating PolypeptideProteasome Endopeptidase ComplexUbiquitinVasodilator Agents

Identifiers

PMID23686612
PMCPMC3758793
OpenAlexW1997848553

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.