Evidence map›Paper›PMID 35439023›Full record

ArticleScience signaling2022

Protein tyrosine phosphatase 1B regulates miR-208b-argonaute 2 association and thyroid hormone responsiveness in cardiac hypertrophy.

Gérald Coulis, Avinash D Londhe, R Sudheer Sagabala, Yanfen Shi, David P Labbé, Alexandre Bergeron, Pramod Sahadevan, Sherin A Nawaito, Fatiha Sahmi, Marie Josse and 7 more

Open access · greenAbstract read
In one paragraph

Article in Science signaling, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

17 authors at 6 institutions in 3 countries.

Gérald CoulisDepartment of Nanobioscience, College of Nanoscale Science and Engineering, SUNY Polytechnic Institute, Albany, NY 12203, USA.ORCID 0000-0001-5991-9706
Avinash D LondheDepartment of Nanobioscience, College of Nanoscale Science and Engineering, SUNY Polytechnic Institute, Albany, NY 12203, USA.ORCID 0000-0001-6812-4796
R Sudheer SagabalaDepartment of Nanobioscience, College of Nanoscale Science and Engineering, SUNY Polytechnic Institute, Albany, NY 12203, USA.ORCID 0000-0003-3897-9480
Yanfen ShiMontreal Heart Institute, Montreal, QC H1T 1C8, Canada.
David P LabbéDepartment of Medicine, Division of Experimental Medicine, McGill University, Montreal, QC H3G 1Y6, Canada.ORCID 0000-0001-8864-8765
Alexandre BergeronMontreal Heart Institute, Montreal, QC H1T 1C8, Canada.
Pramod SahadevanMontreal Heart Institute, Montreal, QC H1T 1C8, Canada.
Sherin A NawaitoMontreal Heart Institute, Montreal, QC H1T 1C8, Canada.
Fatiha SahmiMontreal Heart Institute, Montreal, QC H1T 1C8, Canada.
Marie JosseDepartment of Nanobioscience, College of Nanoscale Science and Engineering, SUNY Polytechnic Institute, Albany, NY 12203, USA.ORCID 0000-0002-6197-3813
Valérie VinetteRosalind and Morris Goodman Cancer Research Centre, McGill University, Montreal, QC H3A 1A3, Canada.
Marie-Claude GuertinMontreal Health Innovations Coordinating Center, Montreal, QC H1T 1C8, Canada.
Gérard KarsentyDepartment of Genetics and Development, Columbia University, New York, NY 10032, USA.ORCID 0000-0002-9253-7627
Michel L TremblayRosalind and Morris Goodman Cancer Research Centre, McGill University, Montreal, QC H3A 1A3, Canada.ORCID 0000-0002-0281-541X
Jean-Claude TardifMontreal Heart Institute, Montreal, QC H1T 1C8, Canada.ORCID 0000-0002-8200-8983
Bruce G AllenMontreal Heart Institute, Montreal, QC H1T 1C8, Canada.
Benoit BoivinDepartment of Nanobioscience, College of Nanoscale Science and Engineering, SUNY Polytechnic Institute, Albany, NY 12203, USA.ORCID 0000-0003-3306-5970
Montreal Heart Institute · CAMcGill University Health Centre · CASUNY Polytechnic Institute · USColumbia University · USSuez Canal University · EGThe Coordinating Center · US

Funding

Role of the Phosphoprotein Phosphatase PTP1B in Cardiac HypertrophyR15HL138605 · NHLBI · SUNY POLYTECHNIC INSTITUTE · PI BOIVIN, BENOIT · 2017 to 2020
$896k
CIHR MOP-62887NHLBI NIH HHS R15 HL138605
6 · The paper itself

Abstract

Increased production of reactive oxygen species plays an essential role in the pathogenesis of several diseases, including cardiac hypertrophy. In our search to identify redox-sensitive targets that contribute to redox signaling, we found that protein tyrosine phosphatase 1B (PTP1B) was reversibly oxidized and inactivated in hearts undergoing hypertrophy. Cardiomyocyte-specific deletion of PTP1B in mice (PTP1B cKO mice) caused a hypertrophic phenotype that was exacerbated by pressure overload. Furthermore, we showed that argonaute 2 (AGO2), a key component of the RNA-induced silencing complex, was a substrate of PTP1B in cardiomyocytes and in the heart. Our results revealed that phosphorylation at Tyr

Indexed as

MicroRNAsProtein Tyrosine Phosphatase, Non-Receptor Type 1AnimalsCardiomegalyMediator ComplexMiceMyocardiumMyocytes, CardiacMed13 protein, mouseMediator ComplexMicroRNAsProtein Tyrosine Phosphatase, Non-Receptor Type 1Ptpn1 protein, mouse

Identifiers

PMID35439023
PMCPMC9125740
OpenAlexW4224260250

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.