Evidence map›Paper›PMID 29439547›Full record

ArticleInternational journal of molecular sciences2018

Prostaglandin D2-Mediated DP2 and AKT Signal Regulate the Activation of Androgen Receptors in Human Dermal Papilla Cells.

Kwan Ho Jeong, Ji Hee Jung, Jung Eun Kim, Hoon Kang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Signaling pathways in hair aging.Frontiers in cell and developmental biology · 2023
    Review
  9. Article
  10. The physiological and pharmacological roles of prostaglandins in hair growth.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Sustained exposure to prostaglandin DJournal of smooth muscle research = Nihon Heikatsukin Gakkai kikanshi · 2019
    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

4 authors at 1 institution in 1 country.

Kwan Ho JeongDepartment of Dermatology, St. Paul's Hospital, College of Medicine, The Catholic University of Korea, Seoul 02259, Korea. kwanho16@nate.com.ORCID 0000-0002-3631-0866
Ji Hee JungDepartment of Dermatology, St. Paul's Hospital, College of Medicine, The Catholic University of Korea, Seoul 02259, Korea. kpajjh@naver.com.ORCID 0000-0002-6948-7414
Jung Eun KimDepartment of Dermatology, St. Paul's Hospital, College of Medicine, The Catholic University of Korea, Seoul 02259, Korea. mdkjeun@naver.com.
Hoon KangDepartment of Dermatology, St. Paul's Hospital, College of Medicine, The Catholic University of Korea, Seoul 02259, Korea. johnkang@catholic.ac.kr.ORCID 0000-0002-9822-4760
St. Paul's Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostaglandin D2 (PGD2) and prostaglandin D2 receptor 2 (DP2) is known to be an important factor in androgenetic alopecia (AGA). However, the effect of PGD2 in human dermal papilla cells (hDPCs) is not fully understood. The function of PGD2-induced expression of the androgen receptor (AR), DP2, and AKT (protein kinase B) signal were examined by using real time-PCR (qRT-PCR), western blot analysis, immunocytochemistry (ICC), and siRNA transfection system. PGD2 stimulated AR expression and AKT signaling through DP2. PGD2 stimulated AR related factors (transforming growth factor beta 1 (TGFβ1), Creb, lymphoid enhancer binding factor 1 (LEF1), and insulin-like growth factor 1, (IGF-1)) and AKT signaling (GSK3β and Creb) on the AR expression in hDPCs. However, these factors were down-regulated by DP2 antagonist (TM30089) and AKT inhibitor (LY294002) as well as DP2 knockdown in hDPCs decreased AR expression and AKT signaling. Finally, we confirmed that PGD2 stimulates the expression of AR related target genes, and that AKT and its downstream substrates are involved in AR expression on hDPCs. Taken together, our data suggest that PGD2 promotes AR and AKT signal via DP2 in hDPCs, thus, PGD2 and DP2 signal plays a critical role in AR expression. These findings support the additional explanation for the development of AGA involving PGD2-DP2 in hDPCs.

Indexed as

Signal TransductionCells, CulturedCyclic AMP Response Element-Binding ProteinDermisFemaleGlycogen Synthase Kinase 3 betaHair FollicleHumansInsulin-Like Growth Factor ILymphoid Enhancer-Binding Factor 1Middle AgedProstaglandin D2Proto-Oncogene Proteins c-aktReceptors, AndrogenReceptors, ImmunologicReceptors, ProstaglandinCyclic AMP Response Element-Binding ProteinGlycogen Synthase Kinase 3 betaInsulin-Like Growth Factor ILEF1 protein, humanLymphoid Enhancer-Binding Factor 1Prostaglandin D2prostaglandin D2 receptorProto-Oncogene Proteins c-aktReceptors, AndrogenReceptors, ImmunologicReceptors, ProstaglandinTransforming Growth Factor beta1AKTandrogen receptorCRTH2/DP2dermal papilla cellprostaglandin D2

Identifiers

PMID29439547
PMCPMC5855778
OpenAlexW2791100636

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.