Evidence map›Paper›PMID 17675581›Full record

ArticleThe American journal of pathology2007

Targeted skin overexpression of the mineralocorticoid receptor in mice causes epidermal atrophy, premature skin barrier formation, eye abnormalities, and alopecia.

Yannis Sainte Marie, Antoine Toulon, Ralf Paus, Eve Maubec, Aicha Cherfa, Maggy Grossin, Vincent Descamps, Maud Clemessy, Jean-Marie Gasc, Michel Peuchmaur and 3 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01407471 (Interest of Topical Spironolactone's Administration to Prevent Corticoid-induced Epidermal Atrophy), which is not on this map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 6% 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.

NCT01407471 phase2completednot on this mapstarted 2011, after this paper: background citation

Interest of Topical Spironolactone's Administration to Prevent Corticoid-induced Epidermal Atrophy

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2011 to 2012Enrolled26ConditionsCutaneous Atrophy Due to CorticosteroidsArmsClobetasol + Spironolactone, Clobetasol + Placebo, Placebo + Spironolactone, Placebo + Placebo
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. The role of the mineralocorticoid receptor in skin.Molecular and cellular endocrinology · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Glucocorticoid-Induced Skin Atrophy: The Old and the New.Clinical, cosmetic and investigational dermatology · 2020
    Review
  12. Article
  13. Review
  14. Article
  15. GRowing an epidermal tumor.The Journal of investigative dermatology · 2013
    Article
  16. Article
  17. Article
  18. Article
  19. 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 8 institutions in 3 countries.

Yannis Sainte MarieINSERM U772, Collège de France, Université Paris-Descartes, Paris, France.
Antoine Toulon
Ralf Paus
Eve Maubec
Aicha Cherfa
Maggy Grossin
Vincent Descamps
Maud Clemessy
Jean-Marie Gasc
Michel Peuchmaur
Adam Glick
Nicolette Farman
Frederic Jaisser
Inserm · FRHôpital Bichat-Claude-Bernard · FRPennsylvania State University · USUniversité Paris Cité · FRCollège de France · FRHôpital Louis-Mourier · FRHôpital Robert-Debré · FRUniversity of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mineralocorticoid receptor (MR) is a transcription factor of the nuclear receptor family, activation of which by aldosterone enhances salt reabsorption in the kidney. The MR is also expressed in nonclassical aldosterone target cells (brain, heart, and skin), in which its functions are incompletely understood. To explore the functional importance of MR in mammalian skin, we have generated a conditional doxycycline-inducible model of MR overexpression, resulting in double-transgenic (DT) mice [keratin 5-tTa/tetO-human MR (hMR)], targeting the human MR specifically to keratinocytes of the epidermis and hair follicle (HF). Expression of hMR throughout gestation resulted in early postnatal death that could be prevented by antagonizing MR signaling. DT mice exhibited premature epidermal barrier formation at embryonic day 16.5, reduced HF density and epidermal atrophy, increased keratinocyte apoptosis at embryonic day 18.5, and premature eye opening. When hMR expression was initiated after birth to overcome mortality, DT mice developed progressive alopecia and HF cysts, starting 4 months after hMR induction, preceded by dystrophy and cycling abnormalities of pelage HF. In contrast, interfollicular epidermis, vibrissae, and footpad sweat glands in DT mice were normal. This new mouse model reveals novel biological roles of MR signaling and offers an instructive tool for dissecting nonclassical functions of MR signaling in epidermal, hair follicle, and ocular physiology.

Indexed as

Gene Expression RegulationAlopeciaAnimalsApoptosisCell ProliferationEmbryo, MammalianEye AbnormalitiesHair FollicleHumansKeratin-15Keratin-5KeratinocytesMiceMice, TransgenicMineralocorticoid Receptor AntagonistsPhenotypeKeratin-15Keratin-5Krt15 protein, mouseMineralocorticoid Receptor AntagonistsReceptors, CalcitriolReceptors, GlucocorticoidReceptors, Mineralocorticoid

Identifiers

PMID17675581
PMCPMC1959477
OpenAlexW2012614217

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.