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http://purl.uniprot.org/citations/17486067http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17486067http://www.w3.org/2000/01/rdf-schema#comment"p101, the regulatory subunit of phosphatidylinositol-3-kinase-gamma (PI3Kgamma), was recently reported as a common site of retroviral insertion in T-cell lymphomas induced in mice by MoFe2-MuLV, a unique recombinant gammaretrovirus. The common interruption of p101 by retroviral integration suggests that the locus encodes an oncogene whose altered expression is related to the induction of T-cell malignancy. To examine a possible role in the malignant process, p101 was overexpressed in human T-cell lines Molt-4 and Jurkat. Transient overexpression of p101 induced apoptosis in recipient cells; however, stable expression could be established in cells that expressed moderate levels of p101. Constitutive p101 overexpression in those cells conferred significant protection against ultraviolet-induced apoptosis. Protection against apoptotic induction was attributed to p101-mediated activation of the Akt pathway. Constitutive overexpression of p101 enhanced the activity of p110gamma and further sensitized it to activation upon stimulation of G protein-coupled receptor. These findings are the first to implicate altered expression of p101 in malignancy, specifically in T-cell lymphoma. The findings further provide insight into the regulation of p110gamma, indicating that the stoichiometry of p110gamma and p101 are important in regulating PI3Kgamma signaling."xsd:string
http://purl.uniprot.org/citations/17486067http://purl.org/dc/terms/identifier"doi:10.1038/sj.onc.1210504"xsd:string
http://purl.uniprot.org/citations/17486067http://purl.uniprot.org/core/author"Johnson C."xsd:string
http://purl.uniprot.org/citations/17486067http://purl.uniprot.org/core/author"Levy L.S."xsd:string
http://purl.uniprot.org/citations/17486067http://purl.uniprot.org/core/author"Marriott S.J."xsd:string
http://purl.uniprot.org/citations/17486067http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17486067http://purl.uniprot.org/core/name"Oncogene"xsd:string
http://purl.uniprot.org/citations/17486067http://purl.uniprot.org/core/pages"7049-7057"xsd:string
http://purl.uniprot.org/citations/17486067http://purl.uniprot.org/core/title"Overexpression of p101 activates PI3Kgamma signaling in T cells and contributes to cell survival."xsd:string
http://purl.uniprot.org/citations/17486067http://purl.uniprot.org/core/volume"26"xsd:string
http://purl.uniprot.org/citations/17486067http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/17486067
http://purl.uniprot.org/citations/17486067http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/17486067
http://purl.uniprot.org/uniprot/#_L7RT34-mappedCitation-17486067http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17486067
http://purl.uniprot.org/uniprot/#_Q8WYR1-mappedCitation-17486067http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17486067
http://purl.uniprot.org/uniprot/L7RT34http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17486067
http://purl.uniprot.org/uniprot/Q8WYR1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17486067