CareLit Fachartikel

Identification and characterization of FoxP1 as a candidate tumor suppressor gene in neuroblastoma

S Ackermann, B Hero, V Ehemann, H Kocak, A Oberthuer, B Brors, F Westermann, Y Kahlert, M Odenthal, F Berthold, M Fischer · Klinische Pädiatrie · 2011 · Heft 05

Dokument
1078830
CareLit-ID
Jahr
2011
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Klinische Pädiatrie
Autor:innen
S Ackermann, B Hero, V Ehemann, H Kocak, A Oberthuer, B Brors, F Westermann, Y Kahlert, M Odenthal, F Berthold, M Fischer
Ausgabe
Heft 05 / 2011
Seiten
–
Erschienen: 2011-05-05 00:00:00
ISSN
0300-8630

Zusammenfassung

To identify genes differenzially expressed between favourable and unfavourable neuroblastomas (NB), microarray profiles of 476 NB specimens were generated. High expression of FOXP1 (forkhead box P1) was found in favourable NBs. FOXP1 maps to a tumour suppressor locus frequently deleted aggressive NB (3p14) and belongs to a family of winged-helix transcription factors that are involved in processes of cell proliferation, differentiation and neoplastic transformation. FOXP1 down-regulation is associated with unfavourable markers like stage 4, age >18 months, MYCN amplification, unfavourable gene expression-based c…

Schlagworte

Klinische Pädiatrie