The polycomb group protein EZH2 is involved in progression of prostate cancer
- PMID: 12374981
- DOI: 10.1038/nature01075
The polycomb group protein EZH2 is involved in progression of prostate cancer
Abstract
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, that the polycomb group protein enhancer of zeste homolog 2 (EZH2) is overexpressed in hormone-refractory, metastatic prostate cancer. Small interfering RNA (siRNA) duplexes 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.
Comment in
-
Cancer. The silence of the genes.Nature. 2002 Oct 10;419(6907):572-3. doi: 10.1038/419572a. Nature. 2002. PMID: 12374961 No abstract available.
Similar articles
-
Essential role for activation of the Polycomb group (PcG) protein chromatin silencing pathway in metastatic prostate cancer.Cell Cycle. 2006 Aug;5(16):1886-901. doi: 10.4161/cc.5.16.3222. Epub 2006 Aug 15. Cell Cycle. 2006. PMID: 16963837
-
The EZH2 polycomb transcriptional repressor--a marker or mover of metastatic prostate cancer?Cancer Cell. 2002 Nov;2(5):349-50. doi: 10.1016/s1535-6108(02)00187-3. Cancer Cell. 2002. PMID: 12450788 Review.
-
Polycomb-group oncogenes EZH2, BMI1, and RING1 are overexpressed in prostate cancer with adverse pathologic and clinical features.Eur Urol. 2007 Aug;52(2):455-63. doi: 10.1016/j.eururo.2006.11.020. Epub 2006 Nov 17. Eur Urol. 2007. PMID: 17134822
-
Polycomb protein EZH2 regulates tumor invasion via the transcriptional repression of the metastasis suppressor RKIP in breast and prostate cancer.Cancer Res. 2012 Jun 15;72(12):3091-104. doi: 10.1158/0008-5472.CAN-11-3546. Epub 2012 Apr 13. Cancer Res. 2012. PMID: 22505648
-
Structural assembly of Polycomb group protein and Insight of EZH2 in cancer progression: A review.J Cancer Res Ther. 2021 Apr-Jun;17(2):311-326. doi: 10.4103/jcrt.JCRT_1090_19. J Cancer Res Ther. 2021. PMID: 33063698 Review.
Cited by
-
Development and epigenetic regulation of Atypical teratoid/rhabdoid tumors in the context of cell-of-origin and halted cell differentiation.Neurooncol Adv. 2024 Sep 23;6(1):vdae162. doi: 10.1093/noajnl/vdae162. eCollection 2024 Jan-Dec. Neurooncol Adv. 2024. PMID: 39465218 Free PMC article. Review.
-
The VEGFA-Induced MAPK-AKT/PTEN/TGFβ Signal Pathway Enhances Progression and MDR in Gastric Cancer.Genes (Basel). 2024 Sep 27;15(10):1266. doi: 10.3390/genes15101266. Genes (Basel). 2024. PMID: 39457390 Free PMC article.
-
Epithelial-Mesenchymal Plasticity and Epigenetic Heterogeneity in Cancer.Cancers (Basel). 2024 Sep 27;16(19):3289. doi: 10.3390/cancers16193289. Cancers (Basel). 2024. PMID: 39409910 Free PMC article. Review.
-
miR-4448/Girdin/Akt/AMPK axis inhibits EZH2-mediated EMT and tumorigenesis in small-cell lung cancer.Cancer Med. 2024 Oct;13(19):e70093. doi: 10.1002/cam4.70093. Cancer Med. 2024. PMID: 39400978 Free PMC article.
-
Exploring the role of EZH2 modulation in shaping the tumor microenvironment.Epigenomics. 2024;16(19-20):1265-1268. doi: 10.1080/17501911.2024.2410693. Epub 2024 Oct 10. Epigenomics. 2024. PMID: 39387445 No abstract available.
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases

