Evidence map›Paper›PMID 24803544›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2014

Opiorphin is a master regulator of the hypoxic response in corporal smooth muscle cells.

Shibo Fu, Moses Tarndie Tar, Arnold Melman, Kelvin Paul Davies

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Journal of men's health · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Hypoxia-enhanced adhesion of red blood cells in microscale flow.Microcirculation (New York, N.Y. : 1994) · 2017
    Article
  13. Advances in the understanding of priapism.Translational andrology and urology · 2017
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

4 authors at 1 institution in 1 country.

Shibo FuDepartment of Urology and.
Moses Tarndie TarDepartment of Urology and.
Arnold MelmanDepartment of Urology and.
Kelvin Paul DaviesDepartment of Urology and Department of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York, USA kelvin.davies@einstein.yu.edu.
Albert Einstein College of Medicine · US

Funding

Involvement of opiorphins and polyamine synthesis in the development of priapismR01DK087872 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI DAVIES, KELVIN P · 2011 to 2013
$738k
Opiorphin as a master regulator of pathways leading to priapismR56DK087872 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DAVIES, KELVIN P · 2014 to 2014
$115k
NIDDK NIH HHS R01 DK087872NIDDK NIH HHS R01DK087872NIDDK NIH HHS R56 DK087872
6 · The paper itself

Abstract

Men with sickle cell disease (SCD) risk developing priapism. Recognizing that SCD is a disease of hypoxia, we investigated the effect of hypoxia on gene expression in corporal smooth muscle (CSM) cells. Rat CSM cells in vitro were treated with CoCl2 or low oxygen tension to mimic hypoxia. Hypoxic conditions increased expression of genes previously associated with priapism in animal models. Variable coding sequence a1 (Vcsa1; the rat opiorphin homologue, sialorphin), hypoxia-inducible factor 1a (Hif-1a), and A2B adenosine receptor (a2br) were increased by 10-, 4-, and 6-fold, respectively, by treatment with CoCl2, whereas low oxygen tension caused increases in expression of 3-, 4-, and 1.5-fold, respectively. Sialorphin-treated CSM cells increased expression of Hif-1a and a2br by 4-fold, and vcsa1-siRNA treatment reduced expression by ∼50%. Using a Hif-1a inhibitor, we demonstrated up-regulation of a2br by sialorphin is dependent on Hif-1a, and knockdown of vcsa1 expression with vcsa1-siRNA demonstrated that hypoxic-up-regulation of Hif-1a is dependent on vcsa1. In CSM from a SCD mouse, there was 15-fold up-regulation of opiorphin at a life stage prior to priapism. We conclude that in CSM, opiorphins are master regulators of the hypoxic response. Opiorphin up-regulation in response to SCD-associated hypoxia activates CSM "relaxant" pathways; excessive activation of these pathways results in priapism.

Indexed as

Anemia, Sickle CellAnimalsCell HypoxiaCells, CulturedCobaltHypoxia-Inducible Factor 1, alpha SubunitMaleMiceMice, Inbred C57BLMice, SCIDMyocytes, Smooth MusclePenisPriapismProtein PrecursorsRatsRats, Sprague-DawleyCobaltcobaltous chlorideHif1a protein, mouseHif1a protein, ratHypoxia-Inducible Factor 1, alpha SubunitProtein PrecursorsReceptor, Adenosine A2BRNA, Small InterferingSalivary Proteins and PeptidesSmr2 protein, mouseSmr3a protein, mouseSmr3b protein, ratA2B-adenosine receptorhypoxia inducible factor-1apriapismsialorphinsickle cell disease

Identifiers

PMID24803544
PMCPMC4101653
OpenAlexW2108024161

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.