Evidence map›Paper›PMID 18483144›Full record

ReviewPharmacological reviews2008

Anchoring junctions as drug targets: role in contraceptive development.

Dolores D Mruk, Bruno Silvestrini, C Yan Cheng

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacological reviews, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed
17.8field-weighted citation impact, top 1% 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

103 citing papers in PubMed, 137 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Non-hormonal Contraception: Current and Emerging Targets.Advances in experimental medicine and biology · 2025
    Review
  5. Article
  6. Review
  7. Autophagy: A Double-Edged Sword in Male Reproduction.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Tight junctions and their regulation by non-coding RNAs.International journal of biological sciences · 2021
    Review
  14. Article
  15. Microtubule Cytoskeleton and Spermatogenesis-Lesson From Studies of Toxicant Models.Toxicological sciences : an official journal of the Society of Toxicology · 2020
    Review
  16. Article
  17. Redox regulation & sperm function: A proteomic insight.The Indian journal of medical research · 2018
    Review
  18. Cell polarity and cytoskeletons-Lesson from the testis.Seminars in cell & developmental biology · 2018
    Review
  19. Article
  20. Mammalian target of rapamycin (mTOR): a central regulator of male fertility?Critical reviews in biochemistry and molecular biology · 2017
    Review

43 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Dolores D MrukPopulation Council, Center for Biomedical Research, The Mary M Wohlford Laboratory for Male Contraceptive Research, 1230 York Avenue, New York, NY 10065, USA. d-mruk@popcbr.rockefeller.edu
Bruno Silvestrini
C Yan Cheng
Population Council · US

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
An in vivo model to study blood-testis barrier dynamicsR03HD051512 · NICHD · POPULATION COUNCIL · PI CHENG, C. YAN · 2007 to 2008
$143k
NICHD NIH HHS R03 HD051512NICHD NIH HHS R03-HD051512NICHD NIH HHS U01 HD045908NICHD NIH HHS U01-HD045908NICHD NIH HHS U54 HD029990NICHD NIH HHS U54-HD029990
6 · The paper itself

Abstract

In multicellular organisms, cell-cell interactions are mediated in part by cell junctions, which underlie tissue architecture. Throughout spermatogenesis, for instance, preleptotene leptotene spermatocytes residing in the basal compartment of the seminiferous epithelium must traverse the blood-testis barrier to enter the adluminal compartment for continued development. At the same time, germ cells must also remain attached to Sertoli cells, and numerous studies have reported extensive restructuring at the Sertoli-Sertoli and Sertoli-germ cell interface during germ cell movement across the seminiferous epithelium. Furthermore, the proteins and signaling cascades that regulate adhesion between testicular cells have been largely delineated. These findings have unveiled a number of potential "druggable" targets that can be used to induce premature release of germ cells from the seminiferous epithelium, resulting in transient infertility. Herein, we discuss a novel approach with the aim of developing a nonhormonal male contraceptive for future human use, one that involves perturbing adhesion between Sertoli and germ cells in the testis.

Indexed as

Cell CommunicationAdherens JunctionsAnimalsCell AdhesionContraceptive Agents, MaleHumansIntercellular JunctionsMaleSertoli CellsSpermatocytesSpermatogenesisTestisContraceptive Agents, Male

Identifiers

PMID18483144
PMCPMC3023124
OpenAlexW2164929923

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.