Role of the polycomb repressive complex 2 in acute promyelocytic leukemia

被引:203
作者
Villa, Raffaella
Pasini, Diego
Gutierrez, Arantxa
Morey, Lluis
Occhionorelli, Manuela
Vire, Emmanuelle
Nomdedeu, Josep F.
Jenuwein, Thomas
Pelicci, Pier Giuseppe
Minucci, Saverio
Fuks, Francois
Helin, Kristian
Di Croce, Luciano
机构
[1] Ctr Regulacio Genom, Barcelona 08003, Spain
[2] Biotech Res & Innovat Ctr, DK-2200 Copenhagen, Denmark
[3] European Inst Oncol, I-20139 Milan, Italy
[4] Free Univ Brussels, B-1070 Brussels, Belgium
[5] Hosp Santa Creu & Sant Pau, Barcelona 08025, Spain
[6] Vienna Bioctr, Res Inst Mol Pathol, A-1030 Vienna, Austria
[7] Inst Catalana Recerca & Estudis Avancats, Barcelona 08003, Spain
[8] Ctr Regulacio Genom, Barcelona 08003, Spain
关键词
D O I
10.1016/j.ccr.2007.04.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epigenetic changes are common alterations in cancer cells. Here, we have investigated the role of Polycomb group proteins in the establishment and maintenance of the aberrant silencing of tumor suppressor genes during transformation induced by the leukemia-associated PML-RAR alpha fusion protein. We show that in leukemic cells knockdown of SUZ12, a key component of Polycomb repressive complex 2 (PRC2), reverts not only histone modification but also induces DNA demethylation of PML-RAR alpha target genes. This results in promoter reactivation and granulocytic differentiation. Importantly, the epigenetic alterations caused by PML-RAR alpha can be reverted by retinoic acid treatment of primary blasts from leukemic patients. Our results demonstrate that the direct targeting of Polycomb group proteins by an oncogene plays a key role during carcinogenesis.
引用
收藏
页码:513 / 525
页数:13
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