Evidence map›Paper›PMID 37981221›Full record

ArticleThe American journal of pathology2024

Release of miR-29 Target Laminin C2 Improves Skin Repair.

Connor J Robinson, Lalitha Thiagarajan, Rebecca Maynard, Maneesha Aruketty, Jeremy Herrera, Lewis Dingle, Adam Reid, Jason Wong, Heng Cao, James Dooley and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The American journal of pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. LAMC2 Drives Airway Remodeling in COPD via EMT Regulation Through the AKT Pathway.International journal of chronic obstructive pulmonary disease · 2026
    Article
  3. Article
  4. The Genetics of Acne.Annals of human genetics · 2025
    Review
  5. Article
  6. Article
  7. 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

15 authors at 4 institutions in 3 countries.

Connor J RobinsonDivision of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Lalitha ThiagarajanDivision of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Rebecca MaynardDivision of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Maneesha ArukettyDivision of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Jeremy HerreraBlond-McIndoe Laboratory, Division of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Lewis DingleBlond-McIndoe Laboratory, Division of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Adam ReidBlond-McIndoe Laboratory, Division of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Jason WongBlond-McIndoe Laboratory, Division of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Heng CaoDivision of Pharmacy and Optometry, School of Health Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
James DooleyCenter for Brain and Disease Research, Flanders Institute for Biotechnology (VIB), Leuven, Belgium; Department of Microbiology and Immunology, Katholieke Universiteit-University of Leuven, Leuven, Belgium; Laboratory of Lymphocyte Signaling and Development, The Babraham Institute, Cambridge, United Kingdom.
Adrian ListonCenter for Brain and Disease Research, Flanders Institute for Biotechnology (VIB), Leuven, Belgium; Department of Microbiology and Immunology, Katholieke Universiteit-University of Leuven, Leuven, Belgium; Laboratory of Lymphocyte Signaling and Development, The Babraham Institute, Cambridge, United Kingdom.
Daniela MüllhauptDepartment of Biology, Institute of Molecular Health Sciences, Eidgenössische Technische Hochschule Zürich (ETH) Zurich, Zurich, Switzerland.
Paul HiebertDepartment of Biology, Institute of Molecular Health Sciences, Eidgenössische Technische Hochschule Zürich (ETH) Zurich, Zurich, Switzerland.
Hayley HiebertDepartment of Biology, Institute of Molecular Health Sciences, Eidgenössische Technische Hochschule Zürich (ETH) Zurich, Zurich, Switzerland.
Svitlana KurinnaDivision of Cell Matrix Biology and Regenerative Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom. Electronic address: svitlana.kurinna@manchester.ac.uk.
Wellcome Centre for Cell-Matrix Research · GBBoard of the Swiss Federal Institutes of Technology · CHBabraham Institute · GBManchester Academic Health Science Centre · GB

Funding

Medical Research Council MR/X023397/1
6 · The paper itself

Abstract

miRNAs are small noncoding RNAs that regulate mRNA targets in a cell-specific manner. miR-29 is expressed in murine and human skin, where it may regulate functions in skin repair. Cutaneous wound healing model in miR-29a/b1 gene knockout mice was used to identify miR-29 targets in the wound matrix, where angiogenesis and maturation of provisional granulation tissue was enhanced in response to genetic deletion of miR-29. Consistently, antisense-mediated inhibition of miR-29 promoted angiogenesis in vitro by autocrine and paracrine mechanisms. These processes are likely mediated by miR-29 target mRNAs released upon removal of miR-29 to improve cell-matrix adhesion. One of these, laminin (Lam)-c2 (also known as laminin γ2), was strongly up-regulated during skin repair in the wound matrix of knockout mice. Unexpectedly, Lamc2 was deposited in the basal membrane of endothelial cells in blood vessels forming in the granulation tissue of knockout mice. New blood vessels showed punctate interactions between Lamc2 and integrin α

Indexed as

LamininMicroRNAsAnimalsEndothelial CellsHumansMiceMice, KnockoutSignal TransductionSkinLamininMicroRNAsMIRN29 microRNA, mouse

Identifiers

PMID37981221
PMCPMC12178330
OpenAlexW4388837396

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.