Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 23 von 3516

Details

Autor(en) / Beteiligte
Titel
Gene mutations in the PI3K/Akt signaling pathway were related to immune thrombocytopenia pathogenesis
Ist Teil von
  • Medicine (Baltimore), 2023-02, Vol.102 (7), p.e32947-e32947
Ort / Verlag
United States: Lippincott Williams & Wilkins
Erscheinungsjahr
2023
Quelle
MEDLINE
Beschreibungen/Notizen
  • Immune thrombocytopenic (ITP) is an autoimmune bleeding disease with genetic susceptibility. Twenty newly diagnosed active primary ITP patients who had not been treated with glucocorticosteroids, immune globulin or immunosuppressants prior to sampling were enrolled in this study. Bone marrow blood mononuclear cells were used for whole exome sequencing to further elucidation the variant genes of ITP. High-molecular-weight genomic DNA was extracted from freshly frozen bone marrow blood mononuclear cells from 20 active ITP patients. Next, the samples were subjected to molecular genetic analysis by whole-exome sequencing, and the results were confirmed by Sanger sequencing. The signaling pathways and cellular processes associated with the mutated genes were identified with gene ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses. The results showed that there were 3998 missense mutations involving 2269 genes in more than 10 individuals. Unique genetic variants including phosphatase and tensin homolog, insulin receptor, and coagulation factor C homology were the most associated with the pathogenesis of ITP. Functional analysis revealed these mutation genes mainly affect Phosphatidylinositol 3 kinase/serine/threonine kinase B signaling pathways (signal transduction) and platelet activation (immune system). Our finding further demonstrates the functional connections between these variant genes and ITP. Although the substantial mechanism and the impact of genetic variation are required further investigation, the application of next generation sequencing in ITP in this paper is a valuable method to reveal the genetic susceptibility.
Sprache
Englisch
Identifikatoren
ISSN: 0025-7974
eISSN: 1536-5964
DOI: 10.1097/MD.0000000000032947
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9936046

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX