The polycomb group protein EZH2 is involved in progression of prostate cancer

被引:2147
作者
Varambally, S
Dhanasekaran, SM
Zhou, M
Barrette, TR
Kumar-Sinha, C
Sanda, MG
Ghosh, D
Pienta, KJ
Sewalt, RGAB
Otte, AP
Rubin, MA
Chinnaiyan, AM [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Biostat, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Sch Med, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[6] Univ Amsterdam, Biocentrum Amsterdam, Swammerdam Inst Life Sci, NL-1018 TV Amsterdam, Netherlands
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature01075
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Prostate cancer is a leading cause of cancer-related death in males and is second only to lung cancer. Although effective surgical and radiation treatments exist for clinically localized prostate cancer, metastatic prostate cancer remains essentially incurable. Here we show, through gene expression profiling(1), that the polycomb group protein enhancer of zeste homolog 2 (EZH2)(2,3) is overexpressed in hormone-refractory, metastatic prostate cancer. Small interfering RNA (siRNA) duplexes(4) targeted against EZH2 reduce the amounts of EZH2 protein present in prostate cells and also inhibit cell proliferation in vitro. Ectopic expression of EZH2 in prostate cells induces transcriptional repression of a specific cohort of genes. Gene silencing mediated by EZH2 requires the SET domain and is attenuated by inhibiting histone deacetylase activity. Amounts of both EZH2 messenger RNA and EZH2 protein are increased in metastatic prostate cancer; in addition, clinically localized prostate cancers that express higher concentrations of EZH2 show a poorer prognosis. Thus, dysregulated expression of EZH2 may be involved in the progression of prostate cancer, as well as being a marker that distinguishes indolent prostate cancer from those at risk of lethal progression.
引用
收藏
页码:624 / 629
页数:7
相关论文
共 28 条
  • [1] Androgen responsive adult human prostatic epithelial cell lines immortalized by human papillomavirus 18
    Bello, D
    Webber, MM
    Kleinman, HK
    Wartinger, DD
    Rhim, JS
    [J]. CARCINOGENESIS, 1997, 18 (06) : 1215 - 1223
  • [2] Web-based tissue microarray image data analysis: Initial validation testing through prostate cancer Gleason grading
    Bova, GS
    Parmigiani, G
    Epstein, JI
    Wheeler, T
    Mucci, NR
    Rubin, MA
    [J]. HUMAN PATHOLOGY, 2001, 32 (04) : 417 - 427
  • [3] Delineation of prognostic biomarkers in prostate cancer
    Dhanasekaran, SM
    Barrette, TR
    Ghosh, D
    Shah, R
    Varambally, S
    Kurachi, K
    Pienta, KJ
    Rubin, MA
    Chinnaiyan, AM
    [J]. NATURE, 2001, 412 (6849) : 822 - 826
  • [4] Cluster analysis and display of genome-wide expression patterns
    Eisen, MB
    Spellman, PT
    Brown, PO
    Botstein, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) : 14863 - 14868
  • [5] Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells
    Elbashir, SM
    Harborth, J
    Lendeckel, W
    Yalcin, A
    Weber, K
    Tuschl, T
    [J]. NATURE, 2001, 411 (6836) : 494 - 498
  • [6] Mechanisms of transcriptional memory
    Francis, NJ
    Kingston, RE
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2001, 2 (06) : 409 - 421
  • [7] NOVEL ZINC FINGER GENE IMPLICATED AS MYC COLLABORATOR BY RETROVIRALLY ACCELERATED LYMPHOMAGENESIS IN E-MU-MYC TRANSGENIC MICE
    HAUPT, Y
    ALEXANDER, WS
    BARRI, G
    KLINKEN, SP
    ADAMS, JM
    [J]. CELL, 1991, 65 (05) : 753 - 763
  • [8] The oncogene and Polycomb-group gene bmi-1 regulates cell proliferation and senescence through the ink4a locus
    Jacobs, JJL
    Kieboom, K
    Marino, S
    DePinho, RA
    van Lohuizen, M
    [J]. NATURE, 1999, 397 (6715) : 164 - 168
  • [9] Cellular memory of transcriptional states by Polycomb-group proteins
    Jacobs, JJL
    van Lohuizen, M
    [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 1999, 10 (02) : 227 - 235
  • [10] Bmi-1 collaborates with c-Myc in tumorigenesis by inhibiting c-Myc-induced apoptosis via INK4a/ARF
    Jacobs, JJL
    Scheijen, B
    Voncken, JW
    Kieboom, K
    Berns, A
    van Lohuizen, M
    [J]. GENES & DEVELOPMENT, 1999, 13 (20) : 2678 - 2690