Evidence map›Paper›PMID 27651436›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2017

Upregulation of microRNA-205 suppresses vascular endothelial growth factor expression-mediated PI3K/Akt signaling transduction in human keloid fibroblasts.

Gang An, Shuzeng Liang, Chunhong Sheng, Yan Liu, Wei Yao

RetractedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  4. Characterization of the skin keloid microenvironment.Cell communication and signaling : CCS · 2023
    Review
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  12. Review
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  17. Oxidative stress-induced angiogenesis is mediated by miR-205-5p.Journal of cellular and molecular medicine · 2020
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

  • Retraction · 2023-01-11Duplication of/in Image · Manipulation of Images · Original Data and/or Images not Provided and/or not Available · Unreliable Image · Unreliable Results and/or Conclusions · · see also: https://pubpeer.com/publications/A271C5509FA10C2916F5037CDE94A9
  • Retracted
5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Gang AnShandong Provincial Qianfoshan Hospital, Jinan, Shandong 250014, China.
Shuzeng LiangShandong Provincial Qianfoshan Hospital, Jinan, Shandong 250014, China.
Chunhong ShengShandong Provincial Qianfoshan Hospital, Jinan, Shandong 250014, China.
Yan LiuShandong Provincial Qianfoshan Hospital, Jinan, Shandong 250014, China.
Wei YaoShandong Provincial Qianfoshan Hospital, Jinan, Shandong 250014, China.
Shandong Provincial QianFoShan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Keloid is one of the most frustrating problems related to wounding healing and presents a great challenge in clinic. MicroRNAs (miRs) have shown their potential as a novel therapy for the prevention and treatment of keloid. Vascular endothelial growth factor (VEGF) plays a critical role in the regulation of scar development. In the current study, it was hypothesized that miR-205-5p was capable of suppressing keloid formation by inhibiting the VEGF-mediated wound healing cascade. The expression statuses of miR-205-5p and VEGF in clinical keloid tissues and keloid cell line human keloid fibroblasts (HKF) were detected. Then the direct action of miR-205-5p on VEGF gene was assessed using dual-luciferase assay. Thereafter, orchestrated administrations on HKF with miR-205-5p mimic, specific VEGF siRNA, PI3K agonist (740 Y-P), and PI3K inhibitor (LY294002) were performed to reveal the roles of miR-205-5p and VEGF in keloid formation and further explain the mechanism through which miR-205-5p affected the VEGF-mediated signaling transductions. Our results showed that there was significant low expression of miR-205-5p in keloid tissue specimens and the cell line while the expression of VEGF in keloid tissues was augmented. Moreover, miR-205-5p overexpression dramatically impaired the cell viability, induced the cell apoptosis, and inhibited the cell invasion and migration ability in HKF. Based on the detection of dual luciferase assay and detection at protein level, miR-205-5p antagonized the keloids by directly targeting VEGF expression and subsequently inhibiting PI3K/Akt pathway. The current study is the first one demonstrating that miR-205-5p inhibits the pathogenesis of keloids, indicating the potential of miR-205-5p in the development of therapies for prevention and treatment of keloids.

Indexed as

AdolescentAdultCell LineCell SurvivalChild, PreschoolChromonesFemaleFibroblastsHumansKeloidMaleMicroRNAsMiddle AgedMorpholinesPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase Inhibitors2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneChromonesMicroRNAsMIR205, humanMIRN200 microRNA, humanMorpholinesPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProto-Oncogene Proteins c-aktRNA, Small InterferingVascular Endothelial Growth Factor AVEGFA protein, humanAktKeloidmicroRNA-205vascular endothelial growth factor

Identifiers

PMID27651436
PMCPMC5384495
OpenAlexW2522825068

What OpenQuestion holds

Textmetadata
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.