Evidence map›Paper›PMID 32123851›Full record

ArticleFASEB bioAdvances2019

Cyclosporine A inhibits MRTF-SRF signaling through Na

Bastien Burat, Quentin Faucher, Petra Čechová, Hélène Arnion, Florent Di Meo, François-Ludovic Sauvage, Pierre Marquet, Marie Essig

Open access · goldAbstract read
In one paragraph

Article in FASEB bioAdvances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

8 authors at 3 institutions in 2 countries.

Bastien BuratCentre for Biology & Health Research, UMR INSERM 1248 IPPRIT (Individual Profiling and Prevention of RIsks in Transplantation) Limoges University Limoges France.
Quentin FaucherCentre for Biology & Health Research, UMR INSERM 1248 IPPRIT (Individual Profiling and Prevention of RIsks in Transplantation) Limoges University Limoges France.
Petra ČechováDepartment of Biophysics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science Palacký University Olomouc Olomouc Czech Republic.
Hélène ArnionCentre for Biology & Health Research, UMR INSERM 1248 IPPRIT (Individual Profiling and Prevention of RIsks in Transplantation) Limoges University Limoges France.
Florent Di MeoCentre for Biology & Health Research, UMR INSERM 1248 IPPRIT (Individual Profiling and Prevention of RIsks in Transplantation) Limoges University Limoges France.
François-Ludovic SauvageCentre for Biology & Health Research, UMR INSERM 1248 IPPRIT (Individual Profiling and Prevention of RIsks in Transplantation) Limoges University Limoges France.
Pierre MarquetCentre for Biology & Health Research, UMR INSERM 1248 IPPRIT (Individual Profiling and Prevention of RIsks in Transplantation) Limoges University Limoges France.
Marie EssigCentre for Biology & Health Research, UMR INSERM 1248 IPPRIT (Individual Profiling and Prevention of RIsks in Transplantation) Limoges University Limoges France.
Inserm · FRUniversité de Limoges · FRRegional Centre of Advanced Technologies and Materials · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcineurin inhibitors (CNI) are the pillars of immunosuppression in transplantation. However, they display a potent nephrotoxicity whose mechanisms remained widely unsolved. We used an untargeted quantitative proteomic approach (iTRAQ technology) to highlight new targets of CNI in renal proximal tubular cells (RPTCs). CNI-treated RPTCs proteome displayed an over-representation of actin-binding proteins with a CNI-specific expression profile. Cyclosporine A (CsA) induced F-actin remodeling and depolymerization, decreased F-actin-stabilizing, polymerization-promoting cofilin (CFL) oligomers, and inhibited the G-actin-regulated serum response factor (SRF) pathway. Inhibition of CFL canonical phosphorylation pathway reproduced CsA effects; however, S3-R, an analogue of the phosphorylation site of CFL prevented the effects of CsA which suggests that CsA acted independently from the canonical CFL regulation. CFL is known to be regulated by the Na

Indexed as

actin cytoskeletoncofilincyclosporine AMRTF‐SRFNa+/K+‐ATPase

Identifiers

PMID32123851
PMCPMC6996406
OpenAlexW2966197580

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.