Evidence map›Paper›PMID 28774591›Full record

ArticleThe Journal of investigative dermatology2017

Topical ROR Inverse Agonists Suppress Inflammation in Mouse Models of Atopic Dermatitis and Acute Irritant Dermatitis.

Jun Dai, Min-Kyung Choo, Jin Mo Park, David E Fisher

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2017. 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
5.4field-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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Vitamin D Signaling in Psoriasis: Pathogenesis and Therapy.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Review
  13. The Impact of the Circadian Clock on Skin Physiology and Cancer Development.International journal of molecular sciences · 2021
    Review
  14. ROR: Nuclear Receptor for Melatonin or Not?Molecules (Basel, Switzerland) · 2021
    Review
  15. Review
  16. Systems Pharmacology andEvidence-based complementary and alternative medicine : eCAM · 2021
    Article
  17. Article
  18. Review
  19. Toxicological research · 2020
    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

4 authors at 2 institutions in 1 country.

Jun DaiCutaneous Biology Research Center, Massachusetts General Hospital, Charlestown, Massachusetts, USA; School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, People's Republic of China; School of Pharmacy, University of Wisconsin-Madison, Wisconsin, USA.
Min-Kyung ChooCutaneous Biology Research Center, Massachusetts General Hospital, Charlestown, Massachusetts, USA.
Jin Mo ParkCutaneous Biology Research Center, Massachusetts General Hospital, Charlestown, Massachusetts, USA.
David E FisherCutaneous Biology Research Center, Massachusetts General Hospital, Charlestown, Massachusetts, USA. Electronic address: DFISHER3@mgh.harvard.edu.
Massachusetts General Hospital · USUniversity of Wisconsin System · US

Funding

Transcriptional mechanisms and melanomaP01CA163222 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DAVID E FISHER · 2013 to 2026
$25.3M
Growth/differentiation control of keratinocytes by ROR alphaK01AR062132 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI DAI, JUN · 2012 to 2015
$442k
Development of next-generation cancer functional diagnosticsR21CA175907 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FISHER, DAVID E · 2013 to 2014
$411k
NCI NIH HHS P01 CA163222NCI NIH HHS R21 CA175907NIAMS NIH HHS K01 AR062132
6 · The paper itself

Abstract

The retinoic acid receptor-related orphan receptors RORα and RORγ are critical for the functions of specific subsets of T cells and innate lymphoid cells, which are key drivers of inflammatory disease in barrier tissues. Here, we investigate the anti-inflammatory potential of SR1001, a synthetic RORα/γ inverse agonist, in mouse models of atopic dermatitis and acute irritant dermatitis. Topical treatment with SR1001 reduces epidermal and dermal features of MC903-induced atopic dermatitis-like disease and suppresses the production of type 2 cytokines and other inflammatory mediators in lesional skin. In the epidermis, SR1001 treatment blocks MC903-induced expression of TSLP and reverses impaired keratinocyte differentiation. SR1001 is also effective in alleviating acute dermatitis triggered by 12-O-tetradecanoylphorbol-13-acetate. Overall, our results suggest that RORα/γ are important therapeutic targets for cutaneous inflammation and suggest topical usage of inhibitory ligands as an approach to treating skin diseases of inflammatory etiology.

Indexed as

AnimalsCell DifferentiationCytokinesDermatitis, AtopicDermatitis, IrritantDisease Models, AnimalEczemaEpidermisFemaleInflammationKeratinocytesLigandsMiceMice, Inbred C57BLNuclear Receptor Subfamily 1, Group F, Member 1SkinCytokinesLigandsNuclear Receptor Subfamily 1, Group F, Member 1Rora protein, mouseSR1001SulfonamidesThiazoles

Identifiers

PMID28774591
PMCPMC5990371
OpenAlexW2740167057

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.