DAP-kinase loss of expression in various carcinoma and B-cell lymphoma cell lines: possible implications for role as tumor suppressor gene

被引:180
|
作者
Kissil, JL
Feinstein, E
Cohen, O
Jones, PA
Tsai, YC
Knowles, MA
Eydmann, ME
Kimchi, A
机构
[1] WEIZMANN INST SCI, DEPT MOL GENET, IL-76100 REHOVOT, ISRAEL
[2] UNIV SO CALIF, KENNETH NORRIS JR COMPREHENS CANC CTR, LOS ANGELES, CA 90033 USA
[3] MARIE CURIE RES INST, MOL GENET LAB, OXTED RH8 0TL, SURREY, ENGLAND
关键词
serine/threonine kinase; death gene; tumor suppressor; methylation; 5'-azadeoxycytidine;
D O I
10.1038/sj.onc.1201172
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
DAP-kinase is a novel calmodulin dependent serine/threonine kinase that carries ankyrin repeats and the death domain. It was recently isolated, by a functional selection approach of gene cloning, as a positive mediator of programmed cell death. In this study the expression of DAP-kinase was examined in the cell lines derived from various human neoplasms, DAP-kinase mRNA and protein expression were below the limit of detection in eight out of ten neoplastic derived B-cell lines. In six out of 14 examined bladder carcinoma, in three out of five renal cell carcinoma, and in four out of ten tested breast carcinoma cell lines, the DAP-kinase protein levels were below detection limits or lower than 1% compared to the positive cell lines. Interestingly, DAP-kinase expression could be restored in some of the negative bladder carcinoma and B-cell lines by treatment of cells with 5'-azadeoxycytidine that causes DNA demethylation. The high frequency of loss of DAP-kinase expression in human tumor cell lines, and the occasional involvement of methylation in this process raise the possibility that this novel mediator of cell death may function as a tumor suppressor gene.
引用
收藏
页码:403 / 407
页数:5
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