Expression of RASSF1A, an epigenetically silenced tumor suppressor, overcomes resistance to apoptosis induction by interferons

Resistance of human renal cell carcinoma (RCC) and melanoma to the apoptosis-inducing effects of IFNs was postulated to result from epigenetic silencing of genes by DNA methylation, a common feature of human cancers. To reverse silencing, 5-AZA-deoxycytidine (5-AZA-dC) or selective depletion of DNA...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2006-03, Vol.66 (5), p.2785-2793
Hauptverfasser: REU, Frederic J, LEAMAN, Douglas W, MAITRA, Ratan R, SOO IN BAE, CHERKASSKY, Leonid, FOX, Mark W, REMPINSKI, Donald R, BEAULIEU, Normand, MACLEOD, A. Robert, BORDEN, Ernest C
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Sprache:eng
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Zusammenfassung:Resistance of human renal cell carcinoma (RCC) and melanoma to the apoptosis-inducing effects of IFNs was postulated to result from epigenetic silencing of genes by DNA methylation, a common feature of human cancers. To reverse silencing, 5-AZA-deoxycytidine (5-AZA-dC) or selective depletion of DNA methyltransferase 1 (DNMT1) by phosphorothioate oligonucleotide antisense (DNMT1 AS) were employed in cells resistant (400-fold higher TRAIL decoy receptor 1 expression than transduced ACHN cells (real-time reverse transcription-PCR). Results identified RASSF1A as regulated by IFNs and participating in IFN-induced apoptosis at least in part by sensitization to TRAIL.
ISSN:0008-5472
1538-7445
DOI:10.1158/0008-5472.CAN-05-2303