Inhibition of the translocated c-myc in Burkitt's Lymphoma by a PNA complementary to the Eμ enhancer

In Burkitt's Lymphoma there is an up-regulation of the c-myc oncogene caused by its translocation from chromosome 8 to chromosome 14, often close to the E mu enhancer of the immunoglobulin heavy chain locus (IgH). In Burkitt's Lymphoma cells, a peptide nucleic acid complementary for a spec...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2003-10, Vol.63 (19), p.6144-6148
Hauptverfasser: CUTRONA, Giovanna, CARPANETO, Elisabetta M, PONZANELLI, Anna, ULIVI, Massimo, MILLO, Enrico, SCARFI, Sonia, RONCELLA, Silvio, BENATTI, Umberto, BOFFA, Lidia C, FERRARINI, Manlio
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Sprache:eng
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Zusammenfassung:In Burkitt's Lymphoma there is an up-regulation of the c-myc oncogene caused by its translocation from chromosome 8 to chromosome 14, often close to the E mu enhancer of the immunoglobulin heavy chain locus (IgH). In Burkitt's Lymphoma cells, a peptide nucleic acid complementary for a specific unique E mu intronic sequence selectively blocked the expression of the c-myc oncogene under E mu control but not of other c-myc alleles. This Peptide Nucleic Acid also inhibited IgM expression in B cells. The finding that PNAs specific for a regulatory noncoding sequence can block gene expression has important conceptual and practical implications.
ISSN:0008-5472
1538-7445