Evidence map›Paper›PMID 17470551›Full record

ArticleMolecular and cellular biology2007

The pituitary function of androgen receptor constitutes a glucocorticoid production circuit.

Junko Miyamoto, Takahiro Matsumoto, Hiroko Shiina, Kazuki Inoue, Ichiro Takada, Saya Ito, Johbu Itoh, Takeo Minematsu, Takashi Sato, Toshihiko Yanase and 3 more

Expression of concernErratum issuedOpen access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Adrenal cortex renewal in health and disease.Nature reviews. Endocrinology · 2021
    Review
  5. Article
  6. The Sexually Dimorphic Adrenal Cortex: Implications for Adrenal Disease.International journal of molecular sciences · 2021
    Review
  7. Sexual Dimorphism in Glucocorticoid Stress Response.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 2 countries.

Junko MiyamotoInstitute of Molecular and Cellular Biosciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
Takahiro Matsumoto
Hiroko Shiina
Kazuki Inoue
Ichiro Takada
Saya Ito
Johbu Itoh
Takeo Minematsu
Takashi Sato
Toshihiko Yanase
Hajime Nawata
Yoshiyuki R Osamura
Shigeaki Kato
The University of Tokyo · JPKyushu University · JPTokai University · JPJapan Science and Technology Agency · JPNational Student Clearinghouse Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Androgen receptor (AR) mediates diverse androgen actions, particularly reproductive processes in males and females. AR-mediated androgen signaling is considered to also control metabolic processes; however, the molecular basis remains elusive. In the present study, we explored the molecular mechanism of late-onset obesity in male AR null mutant (ARKO) mice. We determined that the obesity was caused by a hypercorticoid state. The negative feedback system regulating glucocorticoid production was impaired in ARKO mice. Male and female ARKO mice exhibited hypertrophic adrenal glands and glucocorticoid overproduction, presumably due to high levels of adrenal corticotropic hormone. The pituitary glands of the ARKO males had increased expression of proopiomelanocortin and decreased expression of the glucocorticoid receptor (GR). There were no overt structural abnormalities and no alteration in the distribution of cell types in the pituitaries of male ARKO mice. Additionally, there was normal production of the other hormones within the glucocorticoid feedback system in both the pituitary and hypothalamus. In a cell line derived from pituitary glands, GR expression was under the positive control of the activated AR. Thus, this study suggests that the activated AR supports the negative feedback regulation of glucocorticoid production via up-regulation of GR expression in the pituitary gland.

Indexed as

Adrenal GlandsAdrenocorticotropic HormoneAnimalsApoptosisCell LineCell ProliferationCorticosteroneDihydrotestosteroneFeedback, PhysiologicalFemaleGene Expression RegulationGlucocorticoidsHypertrophyHypothalamo-Hypophyseal SystemHypothalamusMaleAdrenocorticotropic HormoneCorticosteroneDihydrotestosteroneGlucocorticoidsReceptors, AndrogenReceptors, Glucocorticoid

Identifiers

PMID17470551
PMCPMC1951475
OpenAlexW2160287008

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.