Evidence map›Paper›PMID 35783854›Full record

ArticleFrontiers in cardiovascular medicine2022

Alterations of Cardiac Protein Kinases in Cyclic Nucleotide-Dependent Signaling Pathways in Human Ischemic Heart Failure.

Chunguang Wang, Juuso H Taskinen, Heli Segersvärd, Katariina Immonen, Riikka Kosonen, Johanna M Tolva, Mikko I Mäyränpää, Petri T Kovanen, Vesa M Olkkonen, Juha Sinisalo and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2022. 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
1.5field-weighted citation impact, top 18% 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, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

13 authors at 4 institutions in 1 country.

Chunguang WangMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Juuso H TaskinenMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Heli SegersvärdMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Katariina ImmonenMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Riikka KosonenMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Johanna M TolvaTransplantation Laboratory, Department of Pathology, University of Helsinki, Helsinki, Finland.
Mikko I MäyränpääDepartment of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Petri T KovanenAtherosclerosis Research Laboratory, Wihuri Research Institute, Helsinki, Finland.
Vesa M OlkkonenMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Juha SinisaloHeart and Lung Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Mika LaineMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Ilkka TikkanenMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Päivi LakkistoMinerva Foundation Institute for Medical Research, Biomedicum Helsinki 2 U, Helsinki, Finland.
Minerva Foundation · FIHelsinki University Hospital · FIUniversity of Helsinki · FIWihuri Research Institute · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Impaired protein kinase signaling is a hallmark of ischemic heart disease (IHD). Inadequate understanding of the pathological mechanisms limits the development of therapeutic approaches. We aimed to identify the key cardiac kinases and signaling pathways in patients with IHD with an effort to discover potential therapeutic strategies. Methods: Cardiac kinase activity in IHD left ventricle (LV) and the related signaling pathways were investigated by kinomics, transcriptomics, proteomics, and integrated multi-omics approach. Results: Protein kinase A (PKA) and protein kinase G (PKG) ranked on top in the activity shift among the cardiac kinases. In the IHD LVs, PKA activity decreased markedly compared with that of controls (62% reduction, Conclusion: The deficiency in cAMP/PKA signaling pathway is strongly implicated in the pathogenesis of IHD. Natriuretic peptide CNP could be a potential therapeutic target for the modulation of cGMP/PKG signaling.

Indexed as

cAMP-dependent protein kinasecardiac kinomecGMP-dependent protein kinaseischemic heart diseaseischemic heart failurenatriuretic peptidesecond messenger intracellular signaling

Identifiers

PMID35783854
PMCPMC9247256
OpenAlexW4283028556

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.