Details

Autor(en) / Beteiligte

• Kainz, Birgit
• Shehata, Medhat
• Bilban, Martin
• Kienle, Dirk
• Heintel, Daniel
• Krömer‐Holzinger, Elisabeth
• Le, Trang
• Kröber, Alexander
• Heller, Gerwin
• Schwarzinger, Ilse
• Demirtas, Dita
• Chott, Andreas
• Döhner, Hartmut
• Zöchbauer‐Müller, Sabine
• Fonatsch, Christa
• Zielinski, Christoph
• Stilgenbauer, Stephan
• Gaiger, Alexander
• Wagner, Oswald
• Jäger, Ulrich

Titel

Overexpression of the paternally expressed gene 10 (PEG10) from the imprinted locus on chromosome 7q21 in high‐risk B‐cell chronic lymphocytic leukemia

Ist Teil von

• International journal of cancer, 2007-11, Vol.121 (9), p.1984-1993

Ort / Verlag

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Erscheinungsjahr

2007

Link zum Volltext

Quelle

Wiley Online Library Journals Frontfile Complete

Beschreibungen/Notizen

• We report high expression of the maternally imprinted gene PEG10 in high‐risk B‐CLL defined by high LPL mRNA expression. Differential expression was initially identified by microarray analysis and confirmed by real time PCR in 42 B‐CLL patients. mRNA expression ranged from 0.3‐ to 375.4‐fold compared to normal peripheral blood mononuclear cells (PBMNC). Expression levels in CD19+ B‐CLL cells were 100‐fold higher than in B‐cells from healthy donors. PEG10 expression levels in B‐CLL patient samples remained stable over time even after chemotherapy. High PEG10 expression correlated with high LPL expression (p = 0.001) and a positive Coombs' test (p = 0.04). Interestingly, similar expression patterns were observed for the neighbouring imprinted gene sarcoglycan‐ε (SGCE). Monoallelic expression and maintained imprinting of PEG10 were found by allele‐ or methylation‐specific PCR. The intensity of intracellular staining of PEG10 protein corresponded to mRNA levels as confirmed by immunofluorescence staining. Short term knock‐down of PEG10 in B‐CLL cells and HepG2 cells was not associated with changes in cell survival but resulted in a significant change in the expression of 80 genes. However, long term inhibition of PEG10 led to induction of apoptosis in B‐CLL cells. Our data indicate (i) a prognostic value of PEG10 in B‐CLL patients; (ii) specific deregulation of the imprinted locus at 7q21 in high‐risk B‐CLL; (iii) a potential functional and biological role of PEG10 protein expression. Altogether, PEG10 represents a novel marker in B‐CLL. © 2007 Wiley‐Liss, Inc.