Evidence map›Paper›PMID 27822338›Full record

ReviewWorld journal of stem cells2016

Stem cell therapy for the treatment of Leydig cell dysfunction in primary hypogonadism.

Taylor C Peak, Nora M Haney, William Wang, Kenneth J DeLay, Wayne J Hellstrom

Open access · hybridAbstract readReview
In one paragraph

Review in World journal of stem cells, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Acute Effects of Nicotine on Physiological Responses and Sport Performance in Healthy Baseball Players.International journal of environmental research and public health · 2022
    Observational
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Direct conversion of human fibroblasts into functional Leydig-like cells byAmerican journal of translational research · 2018
    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

5 authors at 1 institution in 1 country.

Taylor C PeakTaylor C Peak, Nora M Haney, William Wang, Kenneth J DeLay, Wayne J Hellstrom, Department of Urology, School of Medicine, Tulane University, New Orleans, LA 70112, United States.
Nora M HaneyTaylor C Peak, Nora M Haney, William Wang, Kenneth J DeLay, Wayne J Hellstrom, Department of Urology, School of Medicine, Tulane University, New Orleans, LA 70112, United States.
William WangTaylor C Peak, Nora M Haney, William Wang, Kenneth J DeLay, Wayne J Hellstrom, Department of Urology, School of Medicine, Tulane University, New Orleans, LA 70112, United States.
Kenneth J DeLayTaylor C Peak, Nora M Haney, William Wang, Kenneth J DeLay, Wayne J Hellstrom, Department of Urology, School of Medicine, Tulane University, New Orleans, LA 70112, United States.
Wayne J HellstromTaylor C Peak, Nora M Haney, William Wang, Kenneth J DeLay, Wayne J Hellstrom, Department of Urology, School of Medicine, Tulane University, New Orleans, LA 70112, United States.
Tulane University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The production of testosterone occurs within the Leydig cells of the testes. When production fails at this level from either congenital, acquired, or systemic disorders, the result is primary hypogonadism. While numerous testosterone formulations have been developed, none are yet fully capable of replicating the physiological patterns of testosterone secretion. Multiple stem cell therapies to restore androgenic function of the testes are under investigation. Leydig cells derived from bone marrow, adipose tissue, umbilical cord, and the testes have shown promise for future therapy for primary hypogonadism. In particular, the discovery and utilization of a group of progenitor stem cells within the testes, known as stem Leydig cells (SLCs), has led not only to a better understanding of testicular development, but of treatment as well. When combining this with an understanding of the mechanisms that lead to Leydig cell dysfunction, researchers and physicians will be able to develop stem cell therapies that target the specific step in the steroidogenic process that is deficient. The current preclinical studies highlight the complex nature of regenerating this steroidogenic process and the problems remain unresolved. In summary, there appears to be two current directions for stem cell therapy in male primary hypogonadism. The first method involves differentiating adult Leydig cells from stem cells of various origins from bone marrow, adipose, or embryonic sources. The second method involves isolating, identifying, and transplanting stem Leydig cells into testicular tissue. Theoretically,

Indexed as

Adipose-derived mesenchymal stem cellsBone marrow-derived stem cellsLeydig cellsPrimary hypogonadismStem cell therapyStem Leydig cellsTestosterone

Identifiers

PMID27822338
PMCPMC5080638
OpenAlexW2538234995

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.