Evidence map›Paper›PMID 26940659›Full record

ArticleNature communications2016

Nuclear PTEN functions as an essential regulator of SRF-dependent transcription to control smooth muscle differentiation.

Henrick Horita, Christina L Wysoczynski, Lori A Walker, Karen S Moulton, Marcella Li, Allison Ostriker, Rebecca Tucker, Timothy A McKinsey, Mair E A Churchill, Raphael A Nemenoff and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

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  20. Smooth muscle cell FTO regulates contractile function.American journal of physiology. Heart and circulatory physiology · 2022
    Article
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

11 authors at 1 institution in 1 country.

Henrick HoritaDepartment of Medicine, Division of Renal Diseases and Hypertension, University of Colorado, Anschutz Medical Campus, 12700 East 19th Avenue, C281, Research Complex 2, Room 7101, Aurora, Colorado 80045, USA.
Christina L WysoczynskiDepartment of Pharmacology, University of Colorado, Anschutz Medical Campus, Aurora, Colorado 80045, USA.
Lori A WalkerDepartment of Medicine, Division of Cardiology, University of Colorado, Anschutz Medical Campus, Aurora, Colorado 80045, USA.
Karen S MoultonDepartment of Medicine, Division of Cardiology, University of Colorado, Anschutz Medical Campus, Aurora, Colorado 80045, USA.
Marcella LiDepartment of Medicine, Division of Cardiology, University of Colorado, Anschutz Medical Campus, Aurora, Colorado 80045, USA.
Allison OstrikerDepartment of Medicine, Division of Renal Diseases and Hypertension, University of Colorado, Anschutz Medical Campus, 12700 East 19th Avenue, C281, Research Complex 2, Room 7101, Aurora, Colorado 80045, USA.
Rebecca TuckerDepartment of Medicine, Division of Renal Diseases and Hypertension, University of Colorado, Anschutz Medical Campus, 12700 East 19th Avenue, C281, Research Complex 2, Room 7101, Aurora, Colorado 80045, USA.
Timothy A McKinseyDepartment of Medicine, Division of Cardiology, University of Colorado, Anschutz Medical Campus, Aurora, Colorado 80045, USA.
Mair E A ChurchillDepartment of Pharmacology, University of Colorado, Anschutz Medical Campus, Aurora, Colorado 80045, USA.
Raphael A NemenoffDepartment of Medicine, Division of Renal Diseases and Hypertension, University of Colorado, Anschutz Medical Campus, 12700 East 19th Avenue, C281, Research Complex 2, Room 7101, Aurora, Colorado 80045, USA.
Mary C M Weiser-EvansDepartment of Medicine, Division of Renal Diseases and Hypertension, University of Colorado, Anschutz Medical Campus, 12700 East 19th Avenue, C281, Research Complex 2, Room 7101, Aurora, Colorado 80045, USA.
University of Colorado Anschutz Medical Campus · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
VRAC and Rho in pulmonary EC proliferationP01HL014985 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STENMARK, KURT R. · 1985 to 2019
$35.1M
Reprogramming of mature smooth muscle cells to vascular progenitor cellsR01HL121877 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MARK W. MAJESKY, Mary CM Weiser-Evans · 2015 to 2026
$7.8M
Regulation of Chromatin Signaling in Heart Failure by the BRD4 Bromodomain Protein.R01HL127240 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MCKINSEY, TIMOTHY, SRIVASTAVA, DEEPAK · 2015 to 2022
$6.4M
Regulation of Cardiac Signaling by Class I Histone DeacetylasesR01HL116848 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MCKINSEY, TIMOTHY · 2013 to 2021
$3.1M
PTEN-dependent regulation of SRF transcriptional activity and SMC phenotype controlR01HL123616 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI WEISER-EVANS, MARY CM. · 2015 to 2018
$2.0M
Role of PTEN in Vascular Lesion FormationR01HL088643 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI WEISER-EVANS, MARY CM. · 2009 to 2012
$1.5M
Structural and Functional Studies of the Histone Chaperone CAF-1R01GM111902 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI CHURCHILL, MAIR E · 2014 to 2017
$1.2M
Isoform-Selective HDAC Inhibitors for Age-Associated Diastolic DysfunctionR21AG043822 · NIA · UNIVERSITY OF COLORADO DENVER · PI MCKINSEY, TIMOTHY · 2012 to 2013
$414k
Microenvironmental Endogenous Reprogramming of Differentiated Smooth Muscle CellsR21HL114126 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI WEISER-EVANS, MARY CM. · 2013 to 2014
$410k
NCATS NIH HHS UL1 TR001082NHLBI NIH HHS 1R01 HL088643NHLBI NIH HHS 1R01 HL123616NHLBI NIH HHS 1R21 HL114126NHLBI NIH HHS 2P01 HL014985NHLBI NIH HHS P01 HL014985NHLBI NIH HHS R01 HL088643NHLBI NIH HHS R01 HL116848NHLBI NIH HHS R01 HL121877NHLBI NIH HHS R01 HL123616NHLBI NIH HHS R01 HL127240NHLBI NIH HHS R21 HL114126NIA NIH HHS R21 AG043822NIGMS NIH HHS R01 GM111902
6 · The paper itself

Abstract

Vascular disease progression is associated with marked changes in vascular smooth muscle cell (SMC) phenotype and function. SMC contractile gene expression and, thus differentiation, is under direct transcriptional control by the transcription factor, serum response factor (SRF); however, the mechanisms dynamically regulating SMC phenotype are not fully defined. Here we report that the lipid and protein phosphatase, PTEN, has a novel role in the nucleus by functioning as an indispensible regulator with SRF to maintain the differentiated SM phenotype. PTEN interacts with the N-terminal domain of SRF and PTEN-SRF interaction promotes SRF binding to essential promoter elements in SM-specific genes. Factors inducing phenotypic switching promote loss of nuclear PTEN through nucleo-cytoplasmic translocation resulting in reduced myogenically active SRF, but enhanced SRF activity on target genes involved in proliferation. Overall decreased expression of PTEN was observed in intimal SMCs of human atherosclerotic lesions underlying the potential clinical importance of these findings.

Indexed as

AnimalsCell DifferentiationCells, CulturedGene Expression RegulationHumansMaleMiceMice, KnockoutMice, TransgenicMuscle, Smooth, VascularMyocytes, Smooth MusclePTEN PhosphohydrolaseRatsRats, Sprague-DawleySerum Response FactorPTEN PhosphohydrolasePten protein, mouseSerum Response Factor

Identifiers

PMID26940659
PMCPMC5411712
OpenAlexW2332482109

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.