Evidence map›Paper›PMID 31569377›Full record

ArticleCells2019

Reciprocal Regulation of TRPS1 and miR-221 in Intervertebral Disc Cells.

Letizia Penolazzi, Elisabetta Lambertini, Leticia Scussel Bergamin, Carlotta Gandini, Antonio Musio, Pasquale De Bonis, Michele Cavallo, Roberta Piva

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. The NFATc1/P2X7 receptor relationship in human intervertebral disc cells.Frontiers in cell and developmental biology · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
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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 1 institution in 1 country.

Letizia PenolazziDepartment of Biomedical and Specialty Surgical Sciences, University of Ferrara, 44121 Ferrara, Italy. maria.letizia.penolazzi@unife.it.
Elisabetta LambertiniDepartment of Biomedical and Specialty Surgical Sciences, University of Ferrara, 44121 Ferrara, Italy. elisabetta.lambertini@unife.it.
Leticia Scussel BergaminDepartment of Biomedical and Specialty Surgical Sciences, University of Ferrara, 44121 Ferrara, Italy. scsltc@unife.it.
Carlotta GandiniDepartment of Biomedical and Specialty Surgical Sciences, University of Ferrara, 44121 Ferrara, Italy. carlotta.gandini@stud.unifi.it.
Antonio MusioDepartment of Neurosurgery, S. Anna University Hospital, 44124 Ferrara, Italy. antonio.musio1@unife.it.
Pasquale De BonisDepartment of Neurosurgery, S. Anna University Hospital, 44124 Ferrara, Italy. pasquale.debonis@unife.it.ORCID 0000-0002-9879-8940
Michele CavalloDepartment of Neurosurgery, S. Anna University Hospital, 44124 Ferrara, Italy. michelecavallo@hotmail.com.
Roberta PivaDepartment of Biomedical and Specialty Surgical Sciences, University of Ferrara, 44121 Ferrara, Italy. piv@unife.it.
University of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intervertebral disc (IVD), a moderately moving joint located between the vertebrae, has a limited capacity for self-repair, and treating injured intervertebral discs remains a major challenge. The development of innovative therapies to reverse IVD degeneration relies primarily on the discovery of key molecules that, occupying critical points of regulatory mechanisms, can be proposed as potential intradiscal injectable biological agents. This study aimed to elucidate the underlying mechanism of the reciprocal regulation of two genes differently involved in IVD homeostasis, the miR-221 microRNA and the TRPS1 transcription factor. Human lumbar IVD tissue samples and IVD primary cells were used to specifically evaluate gene expression and perform functional analysis including the luciferase gene reporter assay, chromatin immunoprecipitation, cell transfection with hTRPS1 overexpression vector and antagomiR-221. A high-level expression of TRPS1 was significantly associated with a lower pathological stage, and TRPS1 overexpression strongly decreased miR-221 expression, while increasing the chondrogenic phenotype and markers of antioxidant defense and stemness. Additionally, TRPS1 was able to repress miR-221 expression by associating with its promoter and miR-221 negatively control TRPS1 expression by targeting the

Indexed as

3' Untranslated RegionsAdultAgedCells, CulturedFeedback, PhysiologicalFemaleGene Expression RegulationHumansIntervertebral DiscIntervertebral Disc DegenerationMaleMicroRNAsMiddle AgedPrimary Cell CulturePromoter Regions, GeneticRepressor Proteins3' Untranslated RegionsMicroRNAsMIR221, humanRepressor ProteinsTRPS1 protein, humanintervertebral disc cellsintervertebral disc degenerationmiR-221TRPS1

Identifiers

PMID31569377
PMCPMC6829335
OpenAlexW2975932793

What Socratic 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 Socratic graph.