Evidence map›Paper›PMID 30009778›Full record

ArticleJournal of molecular and cellular cardiology2018

Quantitative temporal analysis of protein dynamics in cardiac remodeling.

Daniel B McClatchy, Yuanhui Ma, David A Liem, Dominic C M Ng, Peipei Ping, John R Yates

Abstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2018. 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
2.4field-weighted citation impact, top 10% 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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  6. Article
  7. Quantitative BONCAT Allows Identification of Newly Synthesized Proteins after Optic Nerve Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  8. Article
  9. GDF15 and Cardiac Cells: Current Concepts and New Insights.International journal of molecular sciences · 2021
    Review
  10. Ultrasound-targeted microbubble destruction-mediatedAnnals of translational medicine · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
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

6 authors at 2 institutions in 1 country.

Daniel B McClatchyDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.
Yuanhui MaDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.
David A LiemThe NIH Big Data to Knowledge (BD2K) Center of Excellence in Biomedical Computing at UCLA, Los Angeles, CA 90095, USA; Department of Physiology, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Dominic C M NgDepartment of Physiology, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Peipei PingThe NIH Big Data to Knowledge (BD2K) Center of Excellence in Biomedical Computing at UCLA, Los Angeles, CA 90095, USA; Department of Physiology, University of California at Los Angeles, Los Angeles, CA 90095, USA; Department of Bioinformatics, University of California at Los Angeles, Los Angeles, CA 90095, USA.; Department of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA.
John R YatesDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA. Electronic address: jyates@scripps.edu.
Scripps Research Institute · USUniversity of California, Los Angeles · US

Funding

TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI MACCOSS, MICHAEL · 2012 to 2021
$20.7M
TRAININGU54GM114833 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LINDSEY, MERRY L., PING, PEIPEI · 2014 to 2017
$13.8M
Omics Phenotyping for Identifying Molecular Signatures of the Healthy and Failing Heart: An Integrated Data Science PlatformR35HL135772 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PING, PEIPEI · 2017 to 2023
$6.4M
NHLBI NIH HHS R35 HL135772NIGMS NIH HHS P41 GM103533NIGMS NIH HHS U54 GM114833
6 · The paper itself

Abstract

Cardiac remodeling (CR) is a complex dynamic process common to many heart diseases. CR is characterized as a temporal progression of global adaptive and maladaptive perturbations. The complex nature of this process clouds a comprehensive understanding of CR, but greater insight into the processes and mechanisms has potential to identify new therapeutic targets. To provide a deeper understanding of this important cardiac process, we applied a new proteomic technique, PALM (Pulse Azidohomoalanine in Mammals), to quantitate the newly-synthesized protein (NSP) changes during the progression of isoproterenol (ISO)-induced CR in the mouse left ventricle. This analysis revealed a complex combination of adaptive and maladaptive alterations at acute and prolonged time points including the identification of proteins not previously associated with CR. We also combined the PALM dataset with our published protein turnover rate dataset to identify putative biochemical mechanisms underlying CR. The novel integration of analyzing NSPs together with their protein turnover rates demonstrated that alterations in specific biological pathways (e.g., inflammation and oxidative stress) are produced by differential regulation of protein synthesis and degradation.

Indexed as

AnimalsHeartHeart FailureHumansIsoproterenolMiceMyocardiumProtein BiosynthesisProteomeVentricular RemodelingIsoproterenolProteomeAzidohomoalanineCardiac remodelingIsoproterenolMetabolic labelingProteomics

Identifiers

PMID30009778
PMCPMC6239217
OpenAlexW2883162000

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.