EDG3 and SHC3 on chromosome 9q22 are co-amplified in human ependymomas (Articolo in rivista)

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  • EDG3 and SHC3 on chromosome 9q22 are co-amplified in human ependymomas (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.canlet.2009.08.023 (literal)
Alternative label
  • MAGRASSI, LORENZO (1,2); Skrap, Miran (4); Arbustini, Eloisa (3); Cassini, Pamela (3); Chiaranda, Ilaria (2); Arienta, Cesare (2); Marziliano, Nicola (3); Inzani, Frediano (3); Pizzolito, Stefano (5) (2010)
    EDG3 and SHC3 on chromosome 9q22 are co-amplified in human ependymomas
    in Cancer letters (Print); ELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS, AMSTERDAM (Paesi Bassi)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • MAGRASSI, LORENZO (1,2); Skrap, Miran (4); Arbustini, Eloisa (3); Cassini, Pamela (3); Chiaranda, Ilaria (2); Arienta, Cesare (2); Marziliano, Nicola (3); Inzani, Frediano (3); Pizzolito, Stefano (5) (literal)
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  • 36 (literal)
Pagina fine
  • 42 (literal)
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  • 290 (literal)
Rivista
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  • 7 (literal)
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  • 1 (literal)
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  • ISI Web of Science (WOS) (literal)
  • Scopu (literal)
  • PubMe (literal)
  • Google Scholar (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • 1) IGM-CNR Pavia; (2) Neurochirurgia Dipartimento - Scienze Chirurgiche Università; (3) Molecular Genetic Laboratory - Transplant Research Area Fondazione IRCCS Policlinico S. Matteo - ; (4) Neurochirurgia Azienda Ospedaliero-Universitaria S. Maria Della Misericordia - ; (5) Department of Pathology - Azienda Ospedaliero-Universitaria S Maria Della Misericordia (literal)
Titolo
  • EDG3 and SHC3 on chromosome 9q22 are co-amplified in human ependymomas (literal)
Abstract
  • By qPCR we found that EDG3 and SHC3 were amplified in 60% of ependymomas but none in choroid plexus papillomas. In ependymomas EDG3 and SHC3 amplification increased Shc3 protein levels while EDG3 was less affected. Both proteins were co-immunoprecipitated from ependymoma and Shc3 was tyrosine phosphorylated thus presumably active. We showed by digestion with N-glycosidase-F that EDG3 was glycosylated indicating that EDG3 protein was not retained in the endoplasmic reticulum. The co-immunoprecipitation of Shc3 and EDG3 proteins from ependymomas with amplification of SHC3 and EDG3 genes suggests that the two proteins co-operate and are important for ependymomas in vivo. (literal)
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