Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia

被引:291
作者
Raval, Aparna
Tanner, Stephan M.
Byrd, John C.
Angerman, Elizabeth B.
Perko, James D.
Chen, Shih-Shih
Hackanson, Bjoern
Grever, Michael R.
Lucas, David M.
MatkoviC, Jennifer J.
Lin, Thomas S.
Kipps, Thomas J.
Murray, Fiona
Weisenburger, Dennis
Sanger, Warren
Lynch, Jane
Watson, Patrice
Jansen, Mary
Yoshinaga, Yuko
Rosenquist, Richard
de Jong, Pieter J.
Coggill, Penny
Beck, Stephan
Lynch, Henry
de la Chapelle, Albert
Plass, Christoph
机构
[1] Ohio State Univ, Ctr Comprehens Canc, Human Canc Gent Program, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43214 USA
[2] Ohio State Univ, Div Hematol & Oncol, Dept Internal Med, Columbus, OH 43214 USA
[3] Childrens Hosp Oakland Res Inst, Oakland, CA 94609 USA
[4] Creighton Univ, Dept Prevent Med & Publ Hlth, Omaha, NE 68178 USA
[5] Wellcome Trust Sanger Inst, Cambridge, England
[6] Univ Calif San Diego, Dept Internal Med, San Diego, CA 92093 USA
[7] Uppsala Univ, Rudbeck Lab, Dept Genet & Pathol, SE-75185 Uppsala, Sweden
[8] Univ Freiburg, Ctr Med, Dept Hematol Oncol, Freiburg, Germany
基金
英国惠康基金;
关键词
D O I
10.1016/j.cell.2007.03.043
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
The heritability of B cell chronic lymphocytic leukemia (CLL) is relatively high; however, no predisposing mutation has been convincingly identified. We show that loss or reduced expression of death-associated protein kinase 1 (DAPK1) underlies cases of heritable predisposition to CLL and the majority of sporadic CLL. Epigenetic silencing of DAPK1 by promoter methylation occurs in almost all sporadic CLL cases. Furthermore, we defined a disease haplotype, which segregates with the CLL phenotype in a large family. DAM expression of the CLL allele is downregulated by 75% in germline cells due to increased HOXB7 binding. In the blood cells from affected family members, promoter methylation results in additional loss of DAM expression. Thus, reduced expression of DAM can result from germline predisposition, as well as epigenetic or somatic events causing or contributing to the CILL phenotype.
引用
收藏
页码:879 / 890
页数:12
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