Evidence map›Paper›PMID 32784909›Full record

ArticleInternational journal of molecular sciences2020

Autophagy Declines with Premature Skin Aging resulting in Dynamic Alterations in Skin Pigmentation and Epidermal Differentiation.

Daiki Murase, Ayumi Kusaka-Kikushima, Akira Hachiya, Rachel Fullenkamp, Anita Stepp, Asuka Imai, Mizuki Ueno, Keigo Kawabata, Yoshito Takahashi, Tadashi Hase and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Regenerative biomaterials · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Monitoring Autophagy in Human Aging: Key Cell Models and Insights.Frontiers in bioscience (Landmark edition) · 2025
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. ModulatingBiomolecules · 2024
    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

13 authors at 2 institutions in 1 country.

Daiki MuraseBiological Science Research, Kao Corporation, Haga 321-3497, Japan.
Ayumi Kusaka-KikushimaBiological Science Research, Kao Corporation, Odawara 250-0002, Japan.
Akira HachiyaPlanning and Implementation, Kao Corporation, Haga 321-3497, Japan.
Rachel FullenkampAmericas Research Laboratories, Kao USA Inc., Cincinnati, OH 45214, USA.
Anita SteppAmericas Research Laboratories, Kao USA Inc., Cincinnati, OH 45214, USA.
Asuka ImaiAmericas Research Laboratories, Kao USA Inc., Cincinnati, OH 45214, USA.ORCID 0000-0001-7927-5709
Mizuki UenoBiological Science Research, Kao Corporation, Odawara 250-0002, Japan.
Keigo KawabataBiological Science Research, Kao Corporation, Odawara 250-0002, Japan.
Yoshito TakahashiBiological Science Research, Kao Corporation, Odawara 250-0002, Japan.
Tadashi HaseCore Technology Sector, Kao Corporation, Sumida 131-0044, Japan.
Atsushi OhuchiBiological Science Research, Kao Corporation, Haga 321-3497, Japan.
Shuhei NakamuraDepartment of Genetics, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Tamotsu YoshimoriDepartment of Genetics, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Kao Corporation (Japan) · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a membrane traffic system that provides sustainable degradation of cellular components for homeostasis, and is thus considered to promote health and longevity, though its activity declines with aging. The present findings show deterioration of autophagy in association with premature skin aging. Autophagy flux was successfully determined in skin tissues, which demonstrated significantly decreased autophagy in hyperpigmented skin such as that seen in senile lentigo. Furthermore, an exacerbated decline in autophagy was confirmed in xerotic hyperpigmentation areas, accompanied by severe dehydration and a barrier defect, which showed correlations with skin physiological conditions. The enhancement of autophagy in skin ex vivo ameliorated skin integrity, including pigmentation and epidermal differentiation. The present results indicate that the restoration of autophagy can contribute to improving premature skin aging by various intrinsic and extrinsic factors via the normalization of protein homeostasis.

Indexed as

AdultAging, PrematureAutophagyCell DifferentiationCell LineEpidermisFemaleGene Expression RegulationHumansKeratinocytesLentigoMaleMiddle AgedRibosomal ProteinsSkinSkin AgingRibosomal ProteinsRPLP0 protein, humanS-Phase Kinase-Associated Proteinsagingautophagyhyperpigmentationkeratinocytemelanosomeskin

Identifiers

PMID32784909
PMCPMC7460956
OpenAlexW3047835630

What OpenQuestion 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 OpenQuestion graph.