Evidence map›Paper›PMID 34486677›Full record

ArticleHistology and histopathology2021

LINC00937 suppresses keloid fibroblast proliferation and extracellular matrix deposition by targeting the miR-28-5p/MC1R axis.

Jing Wan, Xiao-Lei He, Qi-Chao Jian, Zhi-Feng Fan, Ying Shi, Long-Fei Luo

Abstract read
PubMed Publisher
In one paragraph

Article in Histology and histopathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Characterization of the skin keloid microenvironment.Cell communication and signaling : CCS · 2023
    Review
  4. Review
  5. Review
  6. Review
  7. Emerging roles of long non-coding RNAs in keloids.Frontiers in cell and developmental biology · 2022
    Review
  8. 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

6 authors.

Jing Wan *Department of Dermatology, Renmin Hospital of Wuhan University, Wuhan, China.
Xiao-Lei He *Department of Dermatology, Renmin Hospital of Wuhan University, Wuhan, China.
Qi-Chao JianDepartment of Dermatology, Huangshi Central Hospital of Edong Healthcare Group, Hubei Polytechnic University, Huangshi, Hubei, China.
Zhi-Feng FanDepartment of Dermatology, Renmin Hospital of Wuhan University, Wuhan, China.
Ying ShiDepartment of Dermatology, Renmin Hospital of Wuhan University, Wuhan, China.
Long-Fei LuoDepartment of Dermatology, Renmin Hospital of Wuhan University, Wuhan, China. luolfei30@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) are the most recently discovered class of noncoding RNAs. LncRNAs play a crucial role in multiple disorders. However, the role and mechanism of action of lncRNAs in keloids remain unclear. Here, qRT-PCR and western blotting assays were performed to determine the expression of genes and proteins, respectively. MTT assays were carried out to measure the proliferation of keloid fibroblasts. In addition, a luciferase activity assay was conducted to investigate the relationships between LINC00937 and miR-28-5p and between miR-28-5p and MC1R. The results showed that LINC00937 and MC1R were decreased, whereas miR-28-5p was increased in keloid tissues. LINC00937 overexpression in keloid fibroblasts could repress the extracellular matrix (ECM) deposition and cell proliferation and promote MC1R expression. Moreover, high expression of miR-28-5p and low expression of LINC00937 were detected in keloid fibroblasts. We further showed that LINC00937 promoted MC1R expression by sponging miR-28-5p. Finally, our data indicated that LINC00937 inhibited the ECM deposition and proliferation of keloid fibroblasts by inhibiting miR-28-5p and facilitating MC1R expression. Overall, LINC00937 suppressed the ECM deposition and proliferation of keloid fibroblasts by acting as an miR-28-5p sponge and promoting MC1R expression. Our data suggested that LINC00937 is a potential target for keloid treatment.

Indexed as

Cell ProliferationAdolescentAdultCells, CulturedExtracellular MatrixFemaleFibroblastsHumansKeloidMaleMicroRNAsMiddle AgedReceptor, Melanocortin, Type 1RNA, Long NoncodingSignal TransductionSkinMC1R protein, humanMicroRNAsMIRN28 microRNA, humanReceptor, Melanocortin, Type 1RNA, Long Noncoding

Identifiers

PMID34486677

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Registered trials

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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.