Evidence map›Paper›PMID 35764212›Full record

ReviewMatrix biology : journal of the International Society for Matrix Biology2022

Tissue mechanics coevolves with fibrillar matrisomes in healthy and fibrotic tissues.

Lawrence J Dooling, Karanvir Saini, Alişya A Anlaş, Dennis E Discher

Open access · greenAbstract readReview
In one paragraph

Review in Matrix biology : journal of the International Society for Matrix Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.3field-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

19 citing papers in PubMed, 39 citations in OpenAlex.

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  13. ALKBH5-mediated mClinical and translational medicine · 2024
    Article
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  18. Article
  19. Dynamic and static biomechanical traits of cardiac fibrosis.Frontiers in bioengineering and biotechnology · 2022
    Review
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

4 authors at 1 institution in 1 country.

Lawrence J DoolingMolecular and Cellular Biophysics Lab, University of Pennsylvania,Philadelphia, PA 19104, USA.
Karanvir SainiMolecular and Cellular Biophysics Lab, University of Pennsylvania,Philadelphia, PA 19104, USA.
Alişya A AnlaşMolecular and Cellular Biophysics Lab, University of Pennsylvania,Philadelphia, PA 19104, USA.
Dennis E DischerMolecular and Cellular Biophysics Lab, University of Pennsylvania,Philadelphia, PA 19104, USA. Electronic address: discher@seas.upenn.edu.
University of Pennsylvania · US

Funding

PSOC@Penn Education and OutreachU54CA193417 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2015 to 2020
$10.5M
Stiff, solid microenvironments induce Chromosome loss and challenge Epigenetic therapiesU01CA254886 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2021 to 2025
$4.3M
Nanoscience of 'Self' - reductionist approaches to hCD47 inhibition of phagocytesR01HL124106 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2014 to 2022
$3.1M
Biomaterial approaches to attenuate macrophage recognition of "self"-signals from cancer cellsF32CA228285 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DOOLING, LAWRENCE J · 2018 to 2020
$187k
NCI NIH HHS F32 CA228285NCI NIH HHS U01 CA254886NCI NIH HHS U54 CA193417NHLBI NIH HHS R01 HL124106
6 · The paper itself

Abstract

Fibrillar proteins are principal components of extracellular matrix (ECM) that confer mechanical properties to tissues. Fibrosis can result from wound repair in nearly every tissue in adults, and it associates with increased ECM density and crosslinking as well as increased tissue stiffness. Such fibrotic tissues are a major biomedical challenge, and an emerging view posits that the altered mechanical environment supports both synthetic and contractile myofibroblasts in a state of persistent activation. Here, we review the matrisome in several fibrotic diseases, as well as normal tissues, with a focus on physicochemical properties. Stiffness generally increases with the abundance of fibrillar collagens, the major constituent of ECM, with similar mathematical trends for fibrosis as well as adult tissues from soft brain to stiff bone and heart development. Changes in expression of other core matrisome and matrisome-associated proteins or proteoglycans contribute to tissue stiffening in fibrosis by organizing collagen, crosslinking ECM, and facilitating adhesion of myofibroblasts. Understanding how ECM composition and mechanics coevolve during fibrosis can lead to better models and help with antifibrotic therapies.

Indexed as

CollagenExtracellular MatrixAdultExtracellular Matrix ProteinsFibrosisHumansProteoglycansCollagenExtracellular Matrix ProteinsProteoglycans

Identifiers

PMID35764212
PMCPMC9990088
OpenAlexW4283525002

What Socratic 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 Socratic graph.