Evidence map›Paper›PMID 24513054›Full record

ReviewSteroids2014

5β-Reduced steroids and human Δ(4)-3-ketosteroid 5β-reductase (AKR1D1).

Mo Chen, Trevor M Penning

Abstract readReview
In one paragraph

Review in Steroids, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 5β-Dihydrosteroids: Formation and Properties.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Steroids in Stroke with Special Reference to Progesterone.Cellular and molecular neurobiology · 2019
    Review
  15. Article
  16. ThePharmacogenomics and personalized medicine · 2019
    Article
  17. Dysregulation of ΔMolecular and cellular endocrinology · 2018
    Article
  18. Intracrine androgen biosynthesis, metabolism and action revisited.Molecular and cellular endocrinology · 2018
    Review
  19. A Role of Endogenous Progesterone in Stroke Cerebroprotection Revealed by the Neural-Specific Deletion of Its Intracellular Receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  20. Planar bile acids in health and disease.Biochimica et biophysica acta. Biomembranes · 2017
    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

2 authors at 1 institution in 1 country.

Mo ChenDepartment of Pharmacology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6160, United States.
Trevor M PenningCenter of Excellence in Environmental Toxicology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6160, United States; Department of Pharmacology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6160, United States. Electronic address: penning@upenn.edu.
University of Pennsylvania · US

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Trevor M Penning · 2006 to 2026
$35.3M
Structure/Function of Steroid Transforming AKR'sR01DK047015 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI PENNING, TREVOR M · 1994 to 2011
$3.2M
Kinetic and structural analysis of human steroid 5beta-reductase (AKR1D1)F32DK089827 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI CHEN, MO · 2011 to 2012
$104k
NIDDK NIH HHS F32 DK089827NIDDK NIH HHS F32-DK089827NIDDK NIH HHS R01 DK047015NIDDK NIH HHS R01-DK47015NIEHS NIH HHS P30 ES013508NIEHS NIH HHS P30-ES13508
6 · The paper itself

Abstract

5β-Reduced steroids are non-planar steroids that have a 90° bend in their structure to create an A/B cis-ring junction. This novel property is required for bile-acids to act as emulsifiers, but in addition 5β-reduced steroids have remarkable physiology and may act as potent tocolytic agents, endogenous cardiac glycosides, neurosteroids, and can act as ligands for orphan and membrane bound receptors. In humans there is only a single 5β-reductase gene AKR1D1, which encodes Δ(4)-3-ketosteroid-5β-reductase (AKR1D1). This enzyme is a member of the aldo-keto reductase superfamily, but possesses an altered catalytic tetrad, in which Glu120 replaces the conserved His residue. This predominant liver enzyme generates all 5β-dihydrosteroids in the C19-C27 steroid series. Mutations exist in the AKR1D1 gene, which result in loss of protein stability and are causative in bile-acid deficiency.

Indexed as

Gene Expression ProfilingHumansOxidation-ReductionOxidoreductasesSteroids3-oxo-5 beta-steroid delta 4-dehydrogenaseOxidoreductasesSteroidsBile acid biosynthesisEnzyme mechanismGeneticsSteroid metabolism

Identifiers

PMID24513054
PMCPMC3971473
OpenAlexW2052427467

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.