Evidence map›Paper›PMID 38892449›Full record

ArticleInternational journal of molecular sciences2024

Modified mRNA-Mediated

Min Ho Song, Jimeen Yoo, Do-A Kwon, Elena Chepurko, Sunghye Cho, Anthony Fargnoli, Roger J Hajjar, Woo Jin Park, Lior Zangi, Dongtak Jeong

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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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

10 authors.

Min Ho SongCollege of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea.ORCID 0000-0003-4191-8160
Jimeen YooCardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10019, USA.
Do-A KwonDepartment of Medicinal & Life Science, College of Science and Convergence Technology, Hanyang University-ERICA, Ansan-si 15588, Republic of Korea.
Elena ChepurkoCardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10019, USA.
Sunghye ChoDepartment of Medicinal & Life Science, College of Science and Convergence Technology, Hanyang University-ERICA, Ansan-si 15588, Republic of Korea.
Anthony FargnoliCardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10019, USA.
Roger J HajjarMass General Brigham Gene and Cell Therapy Institute, Boston, MA 02139, USA.
Woo Jin ParkCollege of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea.
Lior ZangiCardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10019, USA.
Dongtak JeongCardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10019, USA.ORCID 0000-0003-4153-3498

Funding

Cardiomyocyte-specific modified mRNA of Pkm2 for induction of cardiac regeneration in ischemic heart failureR01HL142768 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZANGI, LIOR · 2018 to 2022
$2.1M
Hanyang University HY-202300000002136National Research Foundation of Korea 2021R1A2C1008058National Research Foundation of Korea 2021R1A4A5032463NIH HHS HL142768-01NIH HHS HL14913701
6 · The paper itself

Abstract

Modified mRNAs (modRNAs) are an emerging delivery method for gene therapy. The success of modRNA-based COVID-19 vaccines has demonstrated that modRNA is a safe and effective therapeutic tool. Moreover, modRNA has the potential to treat various human diseases, including cardiac dysfunction. Acute myocardial infarction (MI) is a major cardiac disorder that currently lacks curative treatment options, and MI is commonly accompanied by fibrosis and impaired cardiac function. Our group previously demonstrated that the matricellular protein CCN5 inhibits cardiac fibrosis (CF) and mitigates cardiac dysfunction. However, it remains unclear whether early intervention of CF under stress conditions is beneficial or more detrimental due to potential adverse effects such as left ventricular (LV) rupture. We hypothesized that CCN5 would alleviate the adverse effects of myocardial infarction (MI) through its anti-fibrotic properties under stress conditions. To induce the rapid expression of CCN5, ModRNA-

Indexed as

CCN Intercellular Signaling ProteinsFibrosisGenetic TherapyMyocardial InfarctionRNA, MessengerAnimalsDisease Models, AnimalGene Transfer TechniquesHumansIntracellular Signaling Peptides and ProteinsMaleMiceMice, Inbred C57BLMyocardiumVentricular RemodelingCCN Intercellular Signaling ProteinsIntracellular Signaling Peptides and ProteinsRNA, MessengerWISP-2 protein, mousecardiac fibrosisCCN5heart failure (HF)left ventricular rupturemodified mRNA (modRNA)myocardial infarction (MI)

Identifiers

PMID38892449
PMCPMC11172546

What OpenQuestion holds

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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.