Evidence map›Paper›PMID 22558155›Full record

ArticlePloS one2012

Functional implications of novel human acid sphingomyelinase splice variants.

Cosima Rhein, Philipp Tripal, Angela Seebahn, Alice Konrad, Marcel Kramer, Christine Nagel, Jonas Kemper, Jens Bode, Christiane Mühle, Erich Gulbins and 3 more

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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Acid Sphingomyelinase Is a Modulator of Contextual Fear.International journal of molecular sciences · 2022
    Article
  6. mRNA Expression ofInternational journal of molecular sciences · 2021
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Sphingolipids and their metabolism in physiology and disease.Nature reviews. Molecular cell biology · 2018
    Review
  13. Metabolic Regulation of Apoptosis in Cancer.International review of cell and molecular biology · 2016
    Review
  14. Review
  15. Article
  16. Article
  17. 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

13 authors at 3 institutions in 1 country.

Cosima RheinDepartment of Psychiatry and Psychotherapy, University Hospital, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
Philipp Tripal
Angela Seebahn
Alice Konrad
Marcel Kramer
Christine Nagel
Jonas Kemper
Jens Bode
Christiane Mühle
Erich Gulbins
Martin Reichel
Cord-Michael Becker
Johannes Kornhuber
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEJena University Hospital · DEUniversity of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcid sphingomyelinase (ASM) hydrolyses sphingomyelin and generates the lipid messenger ceramide, which mediates a variety of stress-related cellular processes. The pathological effects of dysregulated ASM activity are evident in several human diseases and indicate an important functional role for ASM regulation. We investigated alternative splicing as a possible mechanism for regulating cellular ASM activity. METHODOLOGY/PRINCIPAL

findingsWe identified three novel ASM splice variants in human cells, termed ASM-5, -6 and -7, which lack portions of the catalytic- and/or carboxy-terminal domains in comparison to full-length ASM-1. Differential expression patterns in primary blood cells indicated that ASM splicing might be subject to regulatory processes. The newly identified ASM splice variants were catalytically inactive in biochemical in vitro assays, but they decreased the relative cellular ceramide content in overexpression studies and exerted a dominant-negative effect on ASM activity in physiological cell models. CONCLUSIONS/SIGNIFICANCE: These findings indicate that alternative splicing of ASM is of functional significance for the cellular stress response, possibly representing a mechanism for maintaining constant levels of cellular ASM enzyme activity.

Indexed as

Alternative SplicingAmino Acid SequenceBlotting, WesternCeramidesCloning, MolecularComputational BiologyDNA PrimersElectrophoresis, CapillaryGene ComponentsHeLa CellsHumansIn Vitro TechniquesIsoenzymesLeukocytes, MononuclearMolecular Sequence DataOligonucleotidesacid sphingomyelinase-1CeramidesDNA PrimersIsoenzymesOligonucleotidesSphingomyelin Phosphodiesterase

Identifiers

PMID22558155
PMCPMC3338701
OpenAlexW2010020469

What OpenQuestion 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 OpenQuestion graph.