Evidence map›Paper›PMID 34204945›Full record

ReviewInternational journal of molecular sciences2021

MRTF: Basic Biology and Role in Kidney Disease.

Maria Zena Miranda, Zsuzsanna Lichner, Katalin Szászi, András Kapus

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.0field-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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Inhibition of the MRTF-A/SRF signaling axis alleviates vocal fold scarring.Matrix biology : journal of the International Society for Matrix Biology · 2025
    Article
  9. Review
  10. Imaging methods to monitor and quantify cell differentiation.Frontiers in cell and developmental biology · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Claudin-2 Mediates the Proximal Tubular Epithelial Cell-Fibroblast Crosstalk via Paracrine CTGF.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Article
  17. Review
  18. Article
  19. Review
  20. 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.

Maria Zena MirandaKeenan Research Centre for Biomedical Science of the St. Michael's Hospital, Toronto, ON M5B 1W8, Canada.
Zsuzsanna LichnerKeenan Research Centre for Biomedical Science of the St. Michael's Hospital, Toronto, ON M5B 1W8, Canada.
Katalin SzásziKeenan Research Centre for Biomedical Science of the St. Michael's Hospital, Toronto, ON M5B 1W8, Canada.ORCID 0000-0002-2490-8422
András KapusKeenan Research Centre for Biomedical Science of the St. Michael's Hospital, Toronto, ON M5B 1W8, Canada.
St. Michael's Hospital · CA

Funding

CIHR CIHR, PJT-162360CIHR MOP-13046CIHR MOP-142409CIHR PJT-148608Kidney Foundation of Canada BRGNatural Sciences and Engineering Research Council of Canada RGPIN-2019-05222
6 · The paper itself

Abstract

A lesser known but crucially important downstream effect of Rho family GTPases is the regulation of gene expression. This major role is mediated via the cytoskeleton, the organization of which dictates the nucleocytoplasmic shuttling of a set of transcription factors. Central among these is myocardin-related transcription factor (MRTF), which upon actin polymerization translocates to the nucleus and binds to its cognate partner, serum response factor (SRF). The MRTF/SRF complex then drives a large cohort of genes involved in cytoskeleton remodeling, contractility, extracellular matrix organization and many other processes. Accordingly, MRTF, activated by a variety of mechanical and chemical stimuli, affects a plethora of functions with physiological and pathological relevance. These include cell motility, development, metabolism and thus metastasis formation, inflammatory responses and-predominantly-organ fibrosis. The aim of this review is twofold: to provide an up-to-date summary about the basic biology and regulation of this versatile transcriptional coactivator; and to highlight its principal involvement in the pathobiology of kidney disease. Acting through both direct transcriptional and epigenetic mechanisms, MRTF plays a key (yet not fully appreciated) role in the induction of a profibrotic epithelial phenotype (PEP) as well as in fibroblast-myofibroblast transition, prime pathomechanisms in chronic kidney disease and renal fibrosis.

Indexed as

Cell MovementCell NucleusCytoskeletonGene Expression RegulationHumansKidney DiseasesMultiprotein ComplexesPromoter Regions, GeneticSerum Response FactorTrans-ActivatorsMRTFA protein, humanMultiprotein ComplexesSerum Response FactorSRF protein, humanTrans-Activatorsactin cytoskeletongene expressionkidney fibrosismyofibroblastnucleocytoplasmic shuttlingprofibrotic epithelial phenotypeRho GTPasestranscription factors

Identifiers

PMID34204945
PMCPMC8199744
OpenAlexW3167906099

What OpenQuestion holds

Textmetadata
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.