SUZ12 Is a Candidate Target of the Non-canonical WNT Pathway in the Progression of Chronic Myeloid Leukemia

被引:24
|
作者
Pizzatti, Luciana [1 ]
Binato, Renata [1 ]
Cofre, Jaime [1 ,2 ]
Gomes, Bernadete E. [1 ]
Dobbin, Jane [3 ]
Haussmann, Maria Emilia [4 ]
D'Azambuja, Denise [4 ]
Bouzas, Luis Fernando [1 ]
Abdelhay, Eliana [1 ]
机构
[1] Inst Nacl Canc, Div Labs CEMO, BR-20230130 Rio De Janeiro, Brazil
[2] Univ Fed Santa Catarina, Lab Embriol Mol, Florianopolis, SC, Brazil
[3] Inst Nacl Canc, Serv Hematol, BR-20230130 Rio De Janeiro, Brazil
[4] Inst Nacl Canc, Div Patol, BR-20230130 Rio De Janeiro, Brazil
来源
GENES CHROMOSOMES & CANCER | 2010年 / 49卷 / 02期
关键词
ACUTE PROMYELOCYTIC LEUKEMIA; DIFFERENTIAL DISPLAY; POLYCOMB; HEMATOPOIESIS; CANCER; EXPRESSION; PROTEINS; BINDING; MARKER; CELLS;
D O I
10.1002/gcc.20722
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Polycomb proteins form multiprotein complexes that repress target genes by chromatin remodeling. In this work, we report that the SUZ12 polycomb gene is over-expressed in bone marrow samples of patients at the blastic phase of chronic myeloid leukemia. We also found a direct interaction between polycomb group genes and the WNT signaling pathway in chronic myeloid leukemia transformation. Electrophoretic mobility shift assay (EMSA), Chromatin immunoprecipitation assay (ChIP), and mass spectrometry assays identified noncanonical WNT pathway members, such as WNT5A and WNT11, bound to the SUZ12 promoter. Immunohistochemistry and immunofluorescence with WNT5A and WNT11 antibodies confirmed nuclear localization. Knockdown of WNTs 1, 5A, and 11 with RNAi approaches showed that WNT members are capable of activating SUZ12 transcription with varying promoter affinities. Finally, we suggest that SUZ12 is blocking cellular differentiation, as SUZ12 knockdown release differentiation programs in chronic myeloid blastic phase (CML-BP) transformed cell line. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:107 / 118
页数:12
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