The gene encoding the prostatic tumor suppressor PSP94 is a target for repression by the Polycomb group protein EZH2

被引:89
作者
Beke, L. [1 ]
Nuytten, M. [1 ]
Van Eynde, A. [1 ]
Beullens, M. [1 ]
Bollen, M. [1 ]
机构
[1] Katholieke Univ Leuven, Fac Med, Dept Mol Cell Biol, Lab Biosignaling & Therapeut, Louvain, Belgium
关键词
EZH2; tumor suppressor; Polycomb group proteins; prostate cancer PSP94; epigenetics;
D O I
10.1038/sj.onc.1210248
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
PSP94, for prostatic secretory protein of 94 amino acids, is secreted by the prostate gland and functions as a suppressor of tumor growth and metastasis. The expression of PSP94 is lost in advanced, hormone-refractory prostate cancer and this correlates with an increased expression of the Polycomb protein EZH2 (enhancer of zeste homolog 2), which represses transcription via trimethylation of histone H3 on Lys27 (H3K27). We show here that these events are causally related and that the MSMB gene, which encodes PSP94, is trimethylated on H3K27 in androgen-refractory, but not in androgen-sensitive prostate cancer cells. Chromatin immunoprecipitation experiments confirmed an association of EZH2 with the MSMB gene. The RNAi-mediated knockdown of EZH2 resulted in a loss of H3K27 trimethylation and an increased expression of the MSMB gene. Conversely, the overexpression of EZH2 was associated with a decreased expression of the MSMB gene. We also demonstrate that MSMB is additionally repressed in androgen-refractory prostate cancer cells by the hypoacetylation of histone H3K9 and the hypermethylation of a CpG island in the promoter region. Our data disclose a hitherto unexplored link between the putative oncogene EZH2 and the tumor suppressor PSP94, and show that MSMB is silenced by EZH2 in advanced prostate cancer cells.
引用
收藏
页码:4590 / 4595
页数:6
相关论文
共 19 条
  • [1] A PSP94-derived peptide PCK3145 inhibits MMP-9 secretion and triggers CD44 cell surface shedding:: Implication in tumor metastasis
    Annabi, B
    Bouzeghrane, M
    Currie, JC
    Hawkins, R
    Dulude, H
    Daigneault, L
    Ruiz, M
    Wisniewski, J
    Garde, S
    Rabbani, SA
    Panchal, C
    Wu, JZJ
    Béliveau, R
    [J]. CLINICAL & EXPERIMENTAL METASTASIS, 2005, 22 (05) : 429 - 439
  • [2] Genome-wide mapping of Polycomb target genes unravels their roles in cell fate transitions
    Bracken, AP
    Dietrich, N
    Pasini, D
    Hansen, KH
    Helin, K
    [J]. GENES & DEVELOPMENT, 2006, 20 (09) : 1123 - 1136
  • [3] EZH2 is downstream of the pRB-E2F pathway, essential for proliferation and amplified in cancer
    Adrian P. Bracken
    Diego Pasini
    Maria Capra
    Elena Prosperini
    Elena Colli
    Kristian Helin
    [J]. The EMBO Journal, 2003, 22 (20) : 5323 - 5335
  • [4] SUZ12 is required for both the histone methyltransferase activity and the silencing function of the EED-EZH2 complex
    Cao, R
    Zhang, Y
    [J]. MOLECULAR CELL, 2004, 15 (01) : 57 - 67
  • [5] Garde SV, 1999, PROSTATE, V38, P118, DOI 10.1002/(SICI)1097-0045(19990201)38:2<118::AID-PROS5>3.0.CO
  • [6] 2-G
  • [7] Silencing of human polycomb target genes is associated with methylation of histone H3 Lys 27
    Kirmizis, A
    Bartley, SM
    Kuzmichev, A
    Margueron, R
    Reinberg, D
    Green, R
    Farnham, PJ
    [J]. GENES & DEVELOPMENT, 2004, 18 (13) : 1592 - 1605
  • [8] A prostate secretory protein94-derived synthetic peptide PCK3145 inhibits VEGF signalling in endothelial cells: Implication in tumor angiogenesis
    Lamy, S
    Ruiz, MT
    Wisniewski, J
    Garde, S
    Rabbani, SA
    Panchal, C
    Wu, JJ
    Annabi, B
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2006, 118 (09) : 2350 - 2358
  • [9] LaTulippe E, 2002, CANCER RES, V62, P4499
  • [10] The diverse functions of histone lysine methylation
    Martin, C
    Zhang, Y
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (11) : 838 - 849