Evidence map›Paper›PMID 22911749›Full record

ArticlePloS one2012

Hydrogen peroxide alters splicing of soluble guanylyl cyclase and selectively modulates expression of splicing regulators in human cancer cells.

Gilbert J Cote, Wen Zhu, Anthony Thomas, Emil Martin, Ferid Murad, Iraida G Sharina

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Role of smooth muscle cells in Cardiovascular Disease.International journal of biological sciences · 2020
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Alternative splicing impairs soluble guanylyl cyclase function in aortic aneurysm.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  12. Review
  13. 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

6 authors at 3 institutions in 1 country.

Gilbert J CoteDepartment of Endocrine Neoplasia and Hormonal Disorders, MD Anderson Cancer Center, Houston, Texas, United States of America.
Wen Zhu
Anthony Thomas
Emil Martin
Ferid Murad
Iraida G Sharina
The University of Texas Health Science Center at Houston · USThe University of Texas MD Anderson Cancer Center · USGeorge Washington University · US

Funding

U OF TEXAS HLTH SCI CTR HOUSTON CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCESUL1RR024148 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2010
$27.9M
Soluble guanylyl cyclase modulation by endogenous elements and exogenous factorsR01HL088128 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MARTIN, EMIL · 2008 to 2012
$2.1M
NCRR NIH HHS UL1 RR024148NHLBI NIH HHS 3R01HL088128NHLBI NIH HHS R01 HL088128
6 · The paper itself

Abstract

backgroundSoluble guanylyl cyclase (sGC) plays a central role in nitric oxide (NO)-mediated signal transduction in the cardiovascular, nervous and gastrointestinal systems. Alternative RNA splicing has emerged as a potential mechanism to modulate sGC expression and activity. C-α1 sGC is an alternative splice form that is resistant to oxidation-induced protein degradation and demonstrates preferential subcellular distribution to the oxidized environment of endoplasmic reticulum (ER). METHODOLOGY/PRINCIPAL

findingsHere we report that splicing of C-α1 sGC can be modulated by H(2)O(2) treatment in BE2 neuroblastoma and MDA-MD-468 adenocarcinoma human cells. In addition, we show that the H(2)O(2) treatment of MDA-MD-468 cells selectively decreases protein levels of PTBP1 and hnRNP A2/B1 splice factors identified as potential α1 gene splicing regulators by in silico analysis. We further demonstrate that down-regulation of PTBP1 by H(2)O(2) occurs at the protein level with variable regulation observed in different breast cancer cells. CONCLUSIONS/SIGNIFICANCE: Our data demonstrate that H(2)O(2) regulates RNA splicing to induce expression of the oxidation-resistant C-α1 sGC subunit. We also report that H(2)O(2) treatment selectively alters the expression of key splicing regulators. This process might play an important role in regulation of cellular adaptation to conditions of oxidative stress.

Indexed as

Alternative SplicingCell Line, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticGuanylate CyclaseHeterogeneous-Nuclear RibonucleoproteinsHumansHydrogen PeroxideNeoplasmsPolypyrimidine Tract-Binding ProteinProteolysisReceptors, Cytoplasmic and NuclearSoluble Guanylyl CyclaseGuanylate CyclaseHeterogeneous-Nuclear RibonucleoproteinsHydrogen PeroxidePolypyrimidine Tract-Binding ProteinPTBP1 protein, humanReceptors, Cytoplasmic and NuclearSoluble Guanylyl Cyclase

Identifiers

PMID22911749
PMCPMC3401163
OpenAlexW2098566677

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.