Evidence map›Paper›PMID 28045574›Full record

ArticleAutophagy2017

Autophagy and KRT8/keratin 8 protect degeneration of retinal pigment epithelium under oxidative stress.

Ahruem Baek, Soojin Yoon, Jean Kim, Yu Mi Baek, Hanna Park, Daehan Lim, Hyewon Chung, Dong-Eun Kim

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
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  4. Piperine alleviates retinal ischemic injury by mediating the APE1 signaling.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
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  15. Article
  16. Review
  17. Proteostasis in aging-associated ocular disease.Molecular aspects of medicine · 2022
    Review
  18. Review
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Ahruem Baeka Department of Bioscience and Biotechnology , Konkuk University , Gwangjin-gu , Seoul , Korea.
Soojin Yoona Department of Bioscience and Biotechnology , Konkuk University , Gwangjin-gu , Seoul , Korea.
Jean Kimb Department of Ophthalmology , Konkuk University School of Medicine , Gwangjin-gu , Seoul , Korea.
Yu Mi Baeka Department of Bioscience and Biotechnology , Konkuk University , Gwangjin-gu , Seoul , Korea.
Hanna Parka Department of Bioscience and Biotechnology , Konkuk University , Gwangjin-gu , Seoul , Korea.
Daehan Limb Department of Ophthalmology , Konkuk University School of Medicine , Gwangjin-gu , Seoul , Korea.
Hyewon Chungb Department of Ophthalmology , Konkuk University School of Medicine , Gwangjin-gu , Seoul , Korea.
Dong-Eun Kima Department of Bioscience and Biotechnology , Konkuk University , Gwangjin-gu , Seoul , Korea.
Konkuk University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contribution of autophagy and regulation of related proteins to the degeneration of retinal pigment epithelium (RPE) in age-related macular degeneration (AMD) remain unknown. We report that upregulation of KRT8 (keratin 8) as well as its phosphorylation are accompanied with autophagy and attenuated with the inhibition of autophagy in RPE cells under oxidative stress. KRT8 appears to have a dual role in RPE pathophysiology. While increased expression of KRT8 following autophagy provides a cytoprotective role in RPE, phosphorylation of KRT8 induces pathologic epithelial-mesenchymal transition (EMT) of RPE cells under oxidative stress, which is mediated by MAPK1/ERK2 (mitogen-activated protein kinase 1) and MAPK3/ERK1. Inhibition of autophagy further promotes EMT, which can be reversed by inhibition of MAPK. Thus, regulated enhancement of autophagy with concurrent increased expression of KRT8 and the inhibition of KRT8 phosphorylation serve to inhibit oxidative stress-induced EMT of RPE cells as well as to prevent cell death, suggesting that pharmacological manipulation of KRT8 upregulation through autophagy with combined inhibition of the MAPK1/3 pathway may be attractive therapeutic strategies for the treatment of AMD.

Indexed as

AutophagyOxidative StressApoptosisAutophagosomesCell LineCell MovementCell NucleusCytoprotectionEpithelial-Mesenchymal TransitionHumansKeratin-8LysosomesMembrane FusionMitogen-Activated Protein Kinase 1Models, BiologicalPhosphorylationKeratin-8Mitogen-Activated Protein Kinase 1Proto-Oncogene Proteins c-aktSuperoxidesTOR Serine-Threonine Kinasesage-related macular degeneration (AMD)apoptosisautophagycell survivalepithelial-mesenchymal transition (EMT)KRT8 (keratin 8)mitogen-activated protein kinases 1 and 3 (MAPK1/3)

Identifiers

PMID28045574
PMCPMC5324842
OpenAlexW2563497525

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.