Evidence map›Paper›PMID 30395847›Full record

ArticleThe Journal of investigative dermatology2019

Potentiation of Psoriasis-Like Inflammation by PCSK9.

Chao Luan, Xundi Chen, Yun Zhu, Jared M Osland, Skyler D Gerber, Melissa Dodds, Yu Hu, Min Chen, Rong Yuan

Open access · greenAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  5. The Third Annual Symposium of the Midwest Aging Consortium.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Article
  6. Review
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  8. Article
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  10. Article
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  14. Article
  15. Review
  16. Mouse Models of Psoriasis: A Comprehensive Review.The Journal of investigative dermatology · 2022
    Review
  17. Review
  18. Article
  19. Review
  20. Variants ofDiagnostics (Basel, Switzerland) · 2021
    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

9 authors at 3 institutions in 2 countries.

Chao LuanJiangsu Key Laboratory of Molecular Biology for Skin Diseases and Sexually Transmitted Infections, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, Jiangsu, China; Department of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Xundi ChenDepartment of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA; Molecular Biology, Microbiology and Biochemistry, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Yun ZhuDepartment of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA; Molecular Biology, Microbiology and Biochemistry, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Jared M OslandDepartment of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Skyler D GerberDepartment of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA; Molecular Biology, Microbiology and Biochemistry, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Melissa DoddsDepartment of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Yu HuJiangsu Key Laboratory of Molecular Biology for Skin Diseases and Sexually Transmitted Infections, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, Jiangsu, China.
Min ChenJiangsu Key Laboratory of Molecular Biology for Skin Diseases and Sexually Transmitted Infections, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, Jiangsu, China. Electronic address: drchenmin@126.com.
Rong YuanDepartment of Internal Medicine, Southern Illinois University School of Medicine, Springfield, Illinois, USA. Electronic address: ryuan@siumed.edu.
Southern Illinois University School of Medicine · USChinese Academy of Medical Sciences Dermatology Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

Depressing Nrip1 Reduces IGF1 Signaling Improves Metabolism and Extends LongevityK01AG046432 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI YUAN, RONG · 2014 to 2018
$726k
Genetic Regulation of Circulating IGF1R21AG034349 · NIA · JACKSON LABORATORY · PI YUAN, RONG · 2010 to 2011
$397k
Identify genetic mechanisms that regulate female sexual maturationR03AG046605 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI YUAN, RONG · 2014 to 2015
$145k
NIA NIH HHS K01 AG046432NIA NIH HHS R03 AG046605NIA NIH HHS R21 AG034349
6 · The paper itself

Abstract

Psoriasis is a systemic inflammatory disease, associated with metabolic disorders, including high level of low-density lipoprotein. PCSK9, which promotes the degradation of low-density lipoprotein receptors and, therefore, the increased concentration of circulating low-density lipoprotein, is also involved in inflammation. This study aims to examine the role of PCSK9 in psoriasis and to investigate the potential of topically applying small interfering RNA targeting Pcsk9 as a psoriasis treatment. We investigated the expression of PCSK9 in lesions of psoriasis patients and imiquimod-induced psoriatic reactions in Pcsk9-knockout and Pcsk9 small interfering RNA-treated mice, and we also used cultured human keratinocytes to investigate the role of PCSK9 in regulating cell proliferation and apoptosis. We found that PCSK9 is overexpressed in psoriatic lesions and that suppressing Pcsk9 can decrease the inflammatory reaction induced by imiquimod treatment and inhibit hyperproliferation of keratinocytes. We also found that suppressing PCSK9 can significantly alter the cell cycle and induce apoptosis of human keratinocytes. Taken together, our findings indicate that PCSK9 plays an important role in psoriasis and may be a therapeutic target.

Indexed as

Gene Expression RegulationAnimalsApoptosisBlotting, WesternCell LineCell ProliferationDisease Models, AnimalFemaleHumansInflammationKeratinocytesMiceMice, Inbred C57BLMice, KnockoutProprotein Convertase 9PsoriasisPcsk9 protein, mouseProprotein Convertase 9RNA

Identifiers

PMID30395847
PMCPMC7546417
OpenAlexW2899379574

What OpenQuestion holds

Textmetadata
LicenceTDM
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.