Evidence map›Paper›PMID 17331889›Full record

ReviewDrug discovery today2007

Expanding the therapeutic use of androgens via selective androgen receptor modulators (SARMs).

Wenqing Gao, James T Dalton

Abstract readReview
In one paragraph

Review in Drug discovery today, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
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

50 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Ostarine blunts the effect of endurance training on submaximal endurance in rats.Naunyn-Schmiedeberg's archives of pharmacology · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Pharmaceutical Care in Sports.Pharmacy (Basel, Switzerland) · 2020
    Article
  19. Drug Repurposing for Triple-Negative Breast Cancer.Journal of personalized medicine · 2020
    Review
  20. 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

2 authors.

Wenqing GaoDivision of Pharmaceutics, College of Pharmacy, The Ohio State University, 500 W 12th Avenue, Columbus, OH 43210, USA.
James T Dalton

Funding

Pharmacology of Nonsteroidal Androgen Receptor LigandsR01DK059800 · NIDDK · OHIO STATE UNIVERSITY · PI DALTON, JAMES T · 2000 to 2007
$2.2M
NIDDK NIH HHS R01 DK059800
6 · The paper itself

Abstract

Selective androgen receptor modulators (SARMs) are a novel class of androgen receptor (AR) ligands that might change the future of androgen therapy dramatically. With improved pharmacokinetic characteristics and tissue-selective pharmacological activities, SARMs are expected to greatly extend the clinical applications of androgens to osteoporosis, muscle wasting, male contraception and diseases of the prostate. Mechanistic studies with currently available SARMs will help to define the contributions of differential tissue distribution, tissue-specific expression of 5alpha-reductase, ligand-specific regulation of gene expression and AR interactions with tissue-specific coactivators to their observed tissue selectivity, and lead to even greater expansion of selective anabolic therapies.

Indexed as

Androgen Receptor AntagonistsAndrogensAndrogen AntagonistsDrug Delivery SystemsDrug DesignFemaleGene Expression RegulationHumansLigandsMaleOrgan SpecificityTissue DistributionAndrogen AntagonistsAndrogen Receptor AntagonistsAndrogensLigands

Identifiers

PMID17331889
PMCPMC2072879

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.