Evidence map›Paper›PMID 30796164›Full record

ArticleThe Journal of biological chemistry2019

Protein phosphatase 2A Aα regulates Aβ protein expression and stability.

Caitlin M O'Connor, Matthew T Hoffa, Sarah E Taylor, Rita A Avelar, Goutham Narla

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 15 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

5 authors at 2 institutions in 1 country.

Caitlin M O'ConnorFrom the Department of Pharmacology, Case Western Reserve University, Cleveland, Ohio 44106.
Matthew T HoffaDepartment of Internal Medicine, Division of Genetic Medicine, University of Michigan, Ann Arbor, Michigan 48109.
Sarah E TaylorDepartment of Pathology, Case Western Reserve University, Cleveland, Ohio 44106.
Rita A AvelarDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109.
Goutham NarlaDepartment of Internal Medicine, Division of Genetic Medicine, University of Michigan, Ann Arbor, Michigan 48109. Electronic address: gnarla@med.umich.edu.
University of Michigan · USCase Western Reserve University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
Training Program in Tumor MicroenvironmentT32CA009676 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Maria G Castro, Analisa Virginia DiFeo · 1992 to 2026
$7.3M
PREDOCTORAL TRAINING PROGRAM IN MOLECULAR THERAPEUTICST32GM008803 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI MIEYAL, JOHN J, NIEMAN, MARVIN THOMAS · 2001 to 2023
$4.2M
Structural and molecular determinants of protein phosphatase 2A in Alzheimer's DiseaseR01CA240993 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NARLA, GOUTHAM, TAYLOR, DEREK JAMES · 2019 to 2023
$3.4M
NRSA Training CoreTL1TR002549 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI HARDING, CLIFFORD V · 2018 to 2022
$2.9M
Small Molecule Activators of PP2A (SMAPs) for Prostate Cancer TherapyR01CA181654 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NARLA, GOUTHAM · 2015 to 2019
$1.9M
Defining the role of endometrial cancer PP2A A-alpha mutations in tumorigenesisF30CA224979 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI TAYLOR, SARAH ELIZABETH · 2018 to 2020
$142k
NCATS NIH HHS TL1 TR002549NCI NIH HHS F30 CA224979NCI NIH HHS R01 CA181654NCI NIH HHS R01 CA240993NCI NIH HHS T32 CA009676NIGMS NIH HHS T32 GM007250NIGMS NIH HHS T32 GM008803
6 · The paper itself

Abstract

Protein phosphatase 2A (PP2A) represses many oncogenic signaling pathways and is an important tumor suppressor. PP2A comprises three distinct subunits and forms through a highly regulated biogenesis process, with the scaffolding A subunit existing as two highly related isoforms, Aα and Aβ. PP2A's tumor-suppressive functions have been intensely studied, and PP2A inactivation has been shown to be a prerequisite for tumor formation. Interestingly, although partial loss of the Aα isoform is growth promoting, complete Aα loss has no transformative properties. Additionally, in cancer patients, Aα is found to be inactivated in a haploinsufficient manner. Using both cellular and

Indexed as

Gene Expression RegulationAmyloid beta-PeptidesAnimalsCRISPR-Cas SystemsFemaleHCT116 CellsHumansMiceMice, Inbred BALB CMice, NudeProtein BindingProtein Phosphatase 2Protein StabilityAmyloid beta-PeptidesProtein Phosphatase 2cancer biologycell signalinginteractomePPP2R1APPP2R1BPR65APR65Bprotein expressionprotein phosphataseprotein phosphatase 2 (PP2A)tumor suppressor gene

Identifiers

PMID30796164
PMCPMC6463732
OpenAlexW2916954261

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.