Evidence map›Paper›PMID 17332525›Full record

ArticleThe Journal of endocrinology2007

Unraveling the molecular targets pertinent to junction restructuring events during spermatogenesis using the Adjudin-induced germ cell depletion model.

Weiliang Xia, Dolores D Mruk, Will M Lee, C Yan Cheng

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of endocrinology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Spermiation: Insights from Studies on the Adjudin Model.Advances in experimental medicine and biology · 2021
    Review
  3. Review
  4. Article
  5. Adjudin--A Male Contraceptive with Other Biological Activities.Recent patents on endocrine, metabolic & immune drug discovery · 2015
    Review
  6. Article
  7. Article
  8. Article
  9. Drug transporters and blood--testis barrier function.The Journal of endocrinology · 2011
    Article
  10. Article
  11. The biology of spermatogenesis: the past, present and future.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2010
    Article
  12. Review
  13. Review
  14. Review
  15. 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

4 authors at 2 institutions in 2 countries.

Weiliang XiaCenter for Biomedical Research, Population Council, 1230 York Avenue, New York, New York 10021, USA.
Dolores D Mruk
Will M Lee
C Yan Cheng
Population Council · USUniversity of Hong Kong · HK

Funding

SPECIALIZED CONTRACEPTIVE DEVELOPMENT RESEARCH CENTERU54HD029990 · NICHD · POPULATION COUNCIL · PI CHENG, C. YAN · 1992 to 2016
$27.7M
Junction Dynamics and Male Fertility RegulationU01HD045908 · NICHD · POPULATION COUNCIL · PI CHENG, C. YAN · 2004 to 2008
$1.3M
NICHD NIH HHS U01 HD045908NICHD NIH HHS U54 HD029990
6 · The paper itself

Abstract

During spermatogenesis, extensive restructuring takes place at the Sertoli-Sertoli and Sertoli-germ cell interface, which is regulated via intriguing interactions among cytokines, proteases, protease inhibitors, kinases, phosphatases, and transcription factors. This in turn determines the steady-state levels of integral membrane proteins at the cell junctions. We sought to further expand these observations using the Adjudin model. Adjudin is a potential male contraceptive that targets Sertoli-germ cell adhesion, causing exfoliation of spermatids and spermatocytes, but not spermatogonia, from the seminiferous epithelium. This model thus provides the means to identify crucial regulatory molecules and signaling pathways pertinent to junction restructuring events during spermatogenesis. In this study, genome-wide expression profiling of rat testes after treatment with Adjudin at the time of extensive junction restructuring was performed. Differentially regulated genes, such as cytokines, proteases, protease inhibitors, cell junction-associated proteins, and transcription factors pertinent to junction restructuring were identified. These data were consistent with earlier findings; however, much new information was obtained which has been deposited at the Gene Expression Omnibus data repository website: http://www.ncbi.nih.gov/geo/ with Accession number: GSE5131. The primary signaling events pertinent to junction restructuring in the testis induced by Adjudin were also delineated using bioinformatics. These findings were also consistent with recently published reports. The identified molecular signatures or targets pertinent to junction dynamics in the testis as reported herein, many of which have not been investigated, thus offer a framework upon which the regulation of junction restructuring events at the Sertoli-Sertoli and Sertoli-germ cell interface pertinent to spermatogenesis can be further studied.

Indexed as

Gene Expression ProfilingOligonucleotide Array Sequence AnalysisAnimalsBase SequenceContraceptive Agents, MaleCytokinesGene ExpressionGerm CellsHydrazinesIndazolesIntercellular JunctionsMaleModels, AnimalModels, GeneticMolecular Sequence DataRats1-(2,4-dichlorobenzyl)indazole-3-carbohydrazideContraceptive Agents, MaleCytokinesHydrazinesIndazolesReceptors, Cytokine

Identifiers

PMID17332525
PMCPMC2804028
OpenAlexW2164760860

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.