Evidence map›Paper›PMID 24940649›Full record

ArticleThe Journal of investigative dermatology2014

Cadherin 11, a miR-675 target, induces N-cadherin expression and epithelial-mesenchymal transition in melasma.

Nan-Hyung Kim, Soo-Hyun Choi, Tae Ryong Lee, Chang-Hoon Lee, Ai-Young Lee

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 44 citations in OpenAlex.

  1. The Pathogenesis of Oxidative Stress-Induced Chloasma and Its Therapeutic Implications.Clinical, cosmetic and investigational dermatology · 2025
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  9. 3,4,5-Tri-Frontiers in cell and developmental biology · 2020
    Article
  10. Review
  11. Article
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  13. Article
  14. From Neural Crest Development to Cancer and Vice Versa: How p75Frontiers in molecular neuroscience · 2018
    Review
  15. Regulation of Human Breast Cancer by the Long Non-Coding RNA H19.International journal of molecular sciences · 2017
    Review
  16. TheOncotarget · 2017
    Article
  17. Review
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Nan-Hyung KimDepartment of Dermatology, Dongguk University Ilsan Hospital, Goyang-si, Korea.
Soo-Hyun ChoiDepartment of Dermatology, Dongguk University Ilsan Hospital, Goyang-si, Korea.
Tae Ryong LeeDepartment of Dermatology, Dongguk University Ilsan Hospital, Goyang-si, Korea; Bioscience Institute, AmorePacific Corporation R&D Center, Yongin-si, Korea.
Chang-Hoon LeeDepartment of Dermatology, Dongguk University Ilsan Hospital, Goyang-si, Korea; College of Pharmacy, Dongguk University, Seoul, Korea.
Ai-Young LeeDepartment of Dermatology, Dongguk University Ilsan Hospital, Goyang-si, Korea. Electronic address: leeay@duih.org.
Dongguk University Ilsan Hospital · KRDongguk University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cadherin 11 (CDH11) was identified as a target of miR-675 by using a luciferase reporter assay. CDH11 expression and miR-675 expression were inversely correlated. CDH11 expression was not detected in melanocytes, but CDH11 expression in fibroblasts and keratinocytes positively influenced melanogenesis via the canonical Wnt and AKT activation pathways in cocultured melanocytes. CDH11 in fibroblasts or keratinocytes induced N-cadherin and Twist1 expression, while decreasing E-cadherin expression. This suggests a role for CDH11 in epithelial-mesenchymal transition. CDH11 in fibroblasts also induced the migration of cocultured melanocytes. N-cadherin knockdown abolished the tyrosinase expression that was induced in CDH11-overexpressing fibroblasts. Collectively, our data indicate that CDH11 in fibroblasts and keratinocytes is a target of miR-675, and could be involved in melanogenesis through the induction of N-cadherin during epithelial-mesenchymal transition.

Indexed as

AdultCadherinsCells, CulturedCoculture TechniquesEpithelial-Mesenchymal TransitionFemaleFibroblastsGene Expression RegulationHumansKeratinocytesMelanocytesMelanosisMicroRNAsMiddle AgedNuclear ProteinsSignal TransductionCadherinsMicroRNAsMIRN675 microRNA, humanNuclear Proteinsosteoblast cadherinTWIST1 protein, humanTwist-Related Protein 1

Identifiers

PMID24940649
OpenAlexW2066081593

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.