Evidence map›Paper›PMID 31852223›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2020

PTEN (Phosphatase and Tensin Homolog) Protects Against Ang II (Angiotensin II)-Induced Pathological Vascular Fibrosis and Remodeling-Brief Report.

Sizhao Lu, Keith A Strand, Marie F Mutryn, Rebecca M Tucker, Austin J Jolly, Seth B Furgeson, Karen S Moulton, Raphael A Nemenoff, Mary C M Weiser-Evans

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. The dark genome in cardiovascular medicine.European heart journal · 2026
    Review
  2. Integrin αScientific reports · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. PTEN: an emerging target in rheumatoid arthritis?Cell communication and signaling : CCS · 2024
    Review
  10. Article
  11. Review
  12. PAI-1 mediates TGF-β1-induced myofibroblast activation in tenocytes via mTOR signaling.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  13. The TNFThe American journal of pathology · 2023
    Article
  14. Article
  15. Review
  16. Smooth muscle αEuropean heart journal open · 2023
    Article
  17. Review
  18. Article
  19. miR-338-3p blocks TGFβ-induced myofibroblast differentiation through the induction of PTEN.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  20. 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

9 authors at 1 institution in 1 country.

Sizhao LuFrom the Division of Renal Diseases and Hypertension, Department of Medicine (S.L., K.A.S., M.F.M., R.M.T., A.J.J., S.B.F., R.A.N., M.C.M.W.-E.), University of Colorado, Anschutz Medical Campus, Aurora.
Keith A StrandFrom the Division of Renal Diseases and Hypertension, Department of Medicine (S.L., K.A.S., M.F.M., R.M.T., A.J.J., S.B.F., R.A.N., M.C.M.W.-E.), University of Colorado, Anschutz Medical Campus, Aurora.
Marie F MutrynFrom the Division of Renal Diseases and Hypertension, Department of Medicine (S.L., K.A.S., M.F.M., R.M.T., A.J.J., S.B.F., R.A.N., M.C.M.W.-E.), University of Colorado, Anschutz Medical Campus, Aurora.
Rebecca M TuckerFrom the Division of Renal Diseases and Hypertension, Department of Medicine (S.L., K.A.S., M.F.M., R.M.T., A.J.J., S.B.F., R.A.N., M.C.M.W.-E.), University of Colorado, Anschutz Medical Campus, Aurora.
Austin J JollyFrom the Division of Renal Diseases and Hypertension, Department of Medicine (S.L., K.A.S., M.F.M., R.M.T., A.J.J., S.B.F., R.A.N., M.C.M.W.-E.), University of Colorado, Anschutz Medical Campus, Aurora.
Seth B FurgesonFrom the Division of Renal Diseases and Hypertension, Department of Medicine (S.L., K.A.S., M.F.M., R.M.T., A.J.J., S.B.F., R.A.N., M.C.M.W.-E.), University of Colorado, Anschutz Medical Campus, Aurora.
Karen S MoultonDivision of Cardiology, Department of Medicine (K.S.M.), University of Colorado, Anschutz Medical Campus, Aurora.
Raphael A NemenoffFrom the Division of Renal Diseases and Hypertension, Department of Medicine (S.L., K.A.S., M.F.M., R.M.T., A.J.J., S.B.F., R.A.N., M.C.M.W.-E.), University of Colorado, Anschutz Medical Campus, Aurora.
Mary C M Weiser-EvansFrom the Division of Renal Diseases and Hypertension, Department of Medicine (S.L., K.A.S., M.F.M., R.M.T., A.J.J., S.B.F., R.A.N., M.C.M.W.-E.), University of Colorado, Anschutz Medical Campus, Aurora.
University of Colorado Anschutz Medical Campus · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Medical Scientist Training ProgramT32GM008497 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI WILSON, CARA C. · 1993 to 2022
$15.2M
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
PREDOCTORAL TRAINING PROGRAM IN PHARMACOLOGYT32GM007635 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI DELL'ACQUA, MARK L · 1985 to 2023
$6.1M
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
Pharmacologic PTEN upregulation: A novel therapeutic approach to prevent pathological vascular remodeling and fibrosisF31HL147393 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STRAND, KEITH · 2019 to 2020
$53k
American Heart Association-American Stroke Association 18POST34030397NCATS NIH HHS UL1 TR001082NCI NIH HHS P30 CA046934NHLBI NIH HHS F31 HL147393NHLBI NIH HHS R01 HL121877NHLBI NIH HHS R01 HL123616NIGMS NIH HHS T32 GM007635NIGMS NIH HHS T32 GM008497
6 · The paper itself

Abstract

objectivePathological vascular remodeling and excessive perivascular fibrosis are major contributors to reduced vessel compliance that exacerbates cardiovascular diseases, for instance, promoting clinically relevant myocardial remodeling. Inflammation plays a significant role in both pathological vascular remodeling and fibrosis. We previously demonstrated that smooth muscle cell-specific PTEN depletion promotes significant vascular fibrosis and accumulation of inflammatory cells. In the current study, we aimed to determine the beneficial role of systemic PTEN elevation on Ang II (angiotensin II)-induced vascular fibrosis and remodeling. Approach and Results: Transgenic mice carrying additional copies of the wild-type

conclusionsSystemic PTEN elevation mediates protection against Ang II-induced vascular inflammation and fibrosis predominantly through effects in resident vascular cells. Our data highly support that pharmacological upregulation of PTEN could be a novel and viable approach for the treatment of pathological vascular fibrosis.

Indexed as

Gene Expression RegulationAngiotensin IIAnimalsBlotting, WesternCells, CulturedDisease Models, AnimalFibrosisFlow CytometryMaleMiceMice, TransgenicMuscle, Smooth, VascularPTEN PhosphohydrolaseRatsRNAVascular DiseasesAngiotensin IIPTEN PhosphohydrolasePten protein, mouseRNAangiotensin IIcardiovascular diseasesfibrosisinflammationvascular remodeling

Identifiers

PMID31852223
PMCPMC7059862
OpenAlexW2995120707

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.