Evidence map›Paper›PMID 22355334›Full record

ArticlePloS one2012

Computational identification of phospho-tyrosine sub-networks related to acanthocyte generation in neuroacanthocytosis.

Lucia De Franceschi, Giovanni Scardoni, Carlo Tomelleri, Adrian Danek, Ruth H Walker, Hans H Jung, Benedikt Bader, Sara Mazzucco, Maria Teresa Dotti, Angela Siciliano and 2 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 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Novel pathogenicNeurology. Genetics · 2019
    Article
  6. Chorea-Acanthocytosis and the Huntington Disease Allele in an Irish Family.Tremor and other hyperkinetic movements (New York, N.Y.) · 2018
    Article
  7. Article
  8. Review
  9. Review
  10. Memory T Cell Migration.Frontiers in immunology · 2015
    Review
  11. Diagnosis and treatment of chorea syndromes.Current neurology and neuroscience reports · 2015
    Review
  12. 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

12 authors at 6 institutions in 4 countries.

Lucia De FranceschiDepartment of Medicine, University of Verona, Verona, Italy. lucia.defranceschi@univr.it
Giovanni Scardoni
Carlo Tomelleri
Adrian Danek
Ruth H Walker
Hans H Jung
Benedikt Bader
Sara Mazzucco
Maria Teresa Dotti
Angela Siciliano
Antonella Pantaleo
Carlo Laudanna
University of Verona · ITKlinik und Poliklinik für Neurologie · DEJames J. Peters VA Medical Center · USUniversity Hospital of Zurich · CHUniversity of Siena · ITUniversity of Turin · IT

Funding

Telethon GGP07007
6 · The paper itself

Abstract

Acanthocytes, abnormal thorny red blood cells (RBC), are one of the biological hallmarks of neuroacanthocytosis syndromes (NA), a group of rare hereditary neurodegenerative disorders. Since RBCs are easily accessible, the study of acanthocytes in NA may provide insights into potential mechanisms of neurodegeneration. Previous studies have shown that changes in RBC membrane protein phosphorylation state affect RBC membrane mechanical stability and morphology. Here, we coupled tyrosine-phosphoproteomic analysis to topological network analysis. We aimed to predict signaling sub-networks possibly involved in the generation of acanthocytes in patients affected by the two core NA disorders, namely McLeod syndrome (MLS, XK-related, Xk protein) and chorea-acanthocytosis (ChAc, VPS13A-related, chorein protein). The experimentally determined phosphoproteomic data-sets allowed us to relate the subsequent network analysis to the pathogenetic background. To reduce the network complexity, we combined several algorithms of topological network analysis including cluster determination by shortest path analysis, protein categorization based on centrality indexes, along with annotation-based node filtering. We first identified XK- and VPS13A-related protein-protein interaction networks by identifying all the interactomic shortest paths linking Xk and chorein to the corresponding set of proteins whose tyrosine phosphorylation was altered in patients. These networks include the most likely paths of functional influence of Xk and chorein on phosphorylated proteins. We further refined the analysis by extracting restricted sets of highly interacting signaling proteins representing a common molecular background bridging the generation of acanthocytes in MLS and ChAc. The final analysis pointed to a novel, very restricted, signaling module of 14 highly interconnected kinases, whose alteration is possibly involved in generation of acanthocytes in MLS and ChAc.

Indexed as

Computational BiologyProtein Interaction MapsAcanthocytesBlotting, WesternChoreaHumansNeuroacanthocytosisPhosphorylationProtein-Tyrosine KinasesProteomicsSyndromeTyrosineProtein-Tyrosine KinasesTyrosine

Identifiers

PMID22355334
PMCPMC3280254
OpenAlexW2114653343

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.