Evidence map›Paper›PMID 37526463›Full record

ArticleAmerican journal of respiratory cell and molecular biology2023

Evaluating Novel Protein Phosphatase 2A Activators as Therapeutics for Emphysema.

Brian Soto, Huma Ahmed, Meshach Pillai, Sangmi S Park, Magdalena Ploszaj, Joshua Reece, Harsha Taluru, Dylan Bobrow, Howard Yu, Pascale Lafortune and 7 more

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Putting a Novel Emphysema Treatment on the SMAP.American journal of respiratory cell and molecular biology · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 1 country.

Brian SotoDepartment of Medicine and.
Huma AhmedDepartment of Medicine and.
Meshach PillaiDepartment of Medicine and.
Sangmi S ParkDepartment of Cell Biology, State University of New York Downstate Health Sciences University, Brooklyn, New York.
Magdalena PloszajDepartment of Medicine and.
Joshua ReeceDepartment of Medicine and.
Harsha TaluruDepartment of Medicine and.
Dylan BobrowDepartment of Medicine and.
Howard YuDepartment of Medicine and.
Pascale LafortuneDepartment of Medicine and.
Bakr JundiDepartment of Medicine and.
Louis CostanzoDepartment of Medicine and.
Abdoulaye J DaboDepartment of Medicine and.
Robert F ForonjyDepartment of Medicine and.
Christian MuellerHorae Gene Therapy Center, University of Massachusetts Medical School, Worcester, Massachusetts.
Michael OhlmeyerAtux Iskay LLC, Plainsboro, New Jersey.
Patrick GeraghtyDepartment of Medicine and.ORCID 0000-0003-1647-5505
State University of New York · USPrinceton Satellite Systems (United States) · USTufts University · US

Funding

Development and Validation of Novel NSG Mouse Models for Human Stem Cell TherapyR24OD018259 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, GREINER, DALE LESLIE · 2014 to 2017
$3.0M
Nuclease free gene editing approaches to treat alpha-1 antitrypsin diseaseR01DK098252 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FLOTTE, TERENCE R. · 2013 to 2022
$3.0M
The Role of HuR in HIV related COPDR01HL162590 · NHLBI · SUNY DOWNSTATE MEDICAL CENTER · PI FORONJY, ROBERT F · 2022 to 2025
$2.9M
Silencing C9or72 with rAAV Mediated RNAiR01NS088689 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BROWN, ROBERT H., MUELLER, CHRISTIAN · 2014 to 2017
$1.6M
NHLBI NIH HHS R01 HL162590NIDDK NIH HHS R01 DK098252NIH HHS R24 OD018259NINDS NIH HHS R01 NS088689NINDS NIH HHS R01-NS088689
6 · The paper itself

Abstract

The activity of PP2A (protein phosphatase 2A), a serine-threonine phosphatase, is reduced by chronic cigarette smoke (SM) exposure and α-1 antitrypsin (AAT) deficiency, and chemical activation of PP2A reduces the loss of lung function in SM-exposed mice. However, the previously studied PP2A-activator tricyclic sulfonamide compound DBK-1154 has low stability to oxidative metabolism, resulting in fast clearance and low systemic exposure. Here we compare the utility of a new more stable PP2A activator, ATUX-792, versus DBK-1154 for the treatment of SM-induced emphysema. ATUX-792 was also tested in human bronchial epithelial cells and a mouse model of AAT deficiency,

Indexed as

EmphysemaPulmonary EmphysemaAnimalsHumansInfantLungMiceMice, KnockoutProtein Phosphatase 2Protein Phosphatase 2cigarette smokeemphysemainflammationprotein phosphatase 2Aα-1 antitrypsin

Identifiers

PMID37526463
PMCPMC10633843
OpenAlexW4385442628

What OpenQuestion holds

Textmetadata
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.