Caspase 8 is deleted or silenced preferentially in childhood neuroblastomas with amplification of MYCN

被引:646
作者
Teitz, T
Wei, T
Valentine, MB
Vanin, EF
Grenet, J
Valentine, VA
Behm, FG
Look, AT
Lahti, JM
Kidd, VJ
机构
[1] St Jude Childrens Res Hosp, Dept Tumor Cell Biol, Memphis, TN 38101 USA
[2] St Jude Childrens Res Hosp, Dept Expt Hematol, Memphis, TN 38101 USA
[3] St Jude Childrens Res Hosp, Dept Expt Oncol, Memphis, TN 38101 USA
[4] St Jude Childrens Res Hosp, Dept Pathol, Memphis, TN 38101 USA
关键词
D O I
10.1038/75007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Caspase 8 is a cysteine protease regulated in both a death-receptor-dependent and -independent manner during apoptosis. Here, we report that the gene for caspase 8 is frequently inactivated in neuroblastoma, a childhood tumor of the peripheral nervous system. The gene is silenced through DNA methylation as well as through gene deletion. Complete inactivation of CASP8 occurred almost exclusively in neuroblastomas with amplification of the oncogene MYCN. Caspase 8-null neuroblastoma cells were resistant to death receptor- and doxorubicin-mediated apoptosis, deficits that were corrected by programmed expression of the enzyme. Thus, caspase 8 acts as a tumor suppressor in neuroblastomas with amplification of MYCN.
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收藏
页码:529 / 535
页数:7
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