Evidence map›Paper›PMID 38243248›Full record

ArticleJournal of translational medicine2024

Selective SERCA2a activator as a candidate for chronic heart failure therapy.

Martina Arici, Shih-Che Hsu, Mara Ferrandi, Paolo Barassi, Carlotta Ronchi, Eleonora Torre, Andrea Luraghi, Gwo-Jyh Chang, Patrizia Ferrari, Giuseppe Bianchi and 3 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Recent Advances in Aptamer-Based Applications in Cardiology.International journal of molecular sciences · 2026
    Review
  6. Review
  7. Development of activators for SERCA2a for heart failure treatments.European journal of medicinal chemistry · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Role of post-translational modifications of Sp1 in cardiovascular diseases.Frontiers in cell and developmental biology · 2024
    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

13 authors.

Martina Arici *Department of Biotechnology and Biosciences, Università Degli Studi di Milano-Bicocca, P.Za Della Scienza 2, 20126, Milan, Italy.
Shih-Che Hsu *CVie Therapeutics Limited, Taipei, 11047, Taiwan.
Mara FerrandiWindtree Therapeutics Inc, Warrington, PA, 18976, USA.
Paolo BarassiWindtree Therapeutics Inc, Warrington, PA, 18976, USA.
Carlotta RonchiDepartment of Biotechnology and Biosciences, Università Degli Studi di Milano-Bicocca, P.Za Della Scienza 2, 20126, Milan, Italy.
Eleonora TorreDepartment of Biotechnology and Biosciences, Università Degli Studi di Milano-Bicocca, P.Za Della Scienza 2, 20126, Milan, Italy.
Andrea LuraghiDepartment of Biotechnology and Biosciences, Università Degli Studi di Milano-Bicocca, P.Za Della Scienza 2, 20126, Milan, Italy.
Gwo-Jyh ChangChang Gung University, Tao-Yuan, 333323, Taiwan.
Patrizia FerrariWindtree Therapeutics Inc, Warrington, PA, 18976, USA.
Giuseppe BianchiWindtree Therapeutics Inc, Warrington, PA, 18976, USA.
Francesco PeriDepartment of Biotechnology and Biosciences, Università Degli Studi di Milano-Bicocca, P.Za Della Scienza 2, 20126, Milan, Italy.
Antonio Zaza *Department of Biotechnology and Biosciences, Università Degli Studi di Milano-Bicocca, P.Za Della Scienza 2, 20126, Milan, Italy. antonio.zaza@unimib.it.
Marcella Rocchetti *Department of Biotechnology and Biosciences, Università Degli Studi di Milano-Bicocca, P.Za Della Scienza 2, 20126, Milan, Italy. marcella.rocchetti@unimib.it.ORCID 0000-0001-9191-4550

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe sarcoplasmic reticulum (SR) Ca

methodsEffects of compound 8 were evaluated in a context of SERCA2a depression, by using streptozotocin-treated rats, a well-known model of diastolic dysfunction. The impact of SERCA2a stimulation by compound 8 was assessed at the cellular level ad in vivo, following i.v. infusion (acute effects) or oral administration (chronic effects).

resultsAs expected from SERCA2a stimulation, compound 8 induced SR Ca

conclusionsThe pharmacological evaluation of compound 8 indicates that it may be a safe and selective drug for a mechanism-based treatment of chronic HF by restoring SERCA2a activity.

Indexed as

Heart FailureAnimalsCalciumCardiotonic AgentsChronic DiseaseEnzyme InhibitorsEtiocholanoloneGuinea PigsMiceMyocytes, CardiacRatsSarcoplasmic Reticulum Calcium-Transporting ATPasesCalciumCardiotonic AgentsEnzyme InhibitorsEtiocholanolonePST3093Sarcoplasmic Reticulum Calcium-Transporting ATPasesDiastolic dysfunctionHeart failureIstaroximePST3093SERCA2aSTZ

Identifiers

PMID38243248
PMCPMC10797746

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.