Remarkable Synergy When Combining EZH2 Inhibitors with YM155 Is H3K27me3-Independent

被引:1
|
作者
Yang, Jun [1 ,2 ,3 ]
Davidoff, Andrew M. [1 ,2 ,3 ,4 ]
机构
[1] St Jude Childrens Res Hosp, Dept Surg, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, St Jude Grad Sch Biomed Sci, Memphis, TN 38105 USA
[3] Univ Tennessee, Coll Med, Hlth Sci Ctr, Dept Pathol, Memphis, TN 38163 USA
[4] Univ Tennessee, Hlth Sci Ctr, Dept Surg, Div Pediat Surg, Memphis, TN 38105 USA
关键词
EZH2; BIRC5; YM155; EPZ5687; EPZ6438; GSK343; PRC2; neuroblastoma; METHYLTRANSFERASE EZH2; SOMATIC MUTATIONS; NEUROBLASTOMA; PHOSPHORYLATION; PRC2; METHYLATION; CELLS; DIFFERENTIATION; TRANSCRIPTION; CHECKPOINT;
D O I
10.3390/cancers15010208
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Systems biology analysis of gene expression across solid tumors identifies a 27 signature that centers on EZH2, the key component of polycomb repressive complex 2. Our study demonstrates that targeting the 27 gene network by the combination of BIRC5 and EZH2 inhibitors achieves remarkable anticancer synergy that is independent of the histone methyltransferase activity of EZH2.Globlal gene expression analysis in combination with pathway analysis shows that combination of YM155, the BIRC5 inhibitor, with EZH2 inhibitors induces unfolded protein response. Targeting multiple molecules in the same biological network may maximize therapeutic efficacy. In this study, we identified a 27-gene module that is highly expressed in solid tumors, encoding actionable targets including EZH2 and BIRC5. The combination of EZH2 inhibitors and a BIRC5 inhibitor, YM155, results in a remarkable synergistic effect. The action of EZH2 inhibitors in this process is independent of the histone methyltransferase activity of polycomb repressive complex 2. Our study reveals a potential therapeutic approach for treating solid tumors by simultaneously targeting EZH2 and BIRC5.
引用
收藏
页数:18
相关论文
共 50 条
  • [1] EZH2/H3K27Me3 and phosphorylated EZH2 predict chemotherapy response and prognosis in ovarian cancer
    Sun, Si
    Yang, Qiang
    Cai, E.
    Huang, Bangxing
    Yin, Feiquan
    Wen, Yiping
    Cai, Ling
    Yang, Ping
    PEERJ, 2020, 8
  • [2] Dynamics of genomic H3K27me3 domains and role of EZH2 during pancreatic endocrine specification
    Xu, Cheng-Ran
    Li, Lin-Chen
    Donahue, Greg
    Ying, Lei
    Zhang, Yu-Wei
    Gadue, Paul
    Zaret, Kenneth S.
    EMBO JOURNAL, 2014, 33 (19) : 2157 - 2170
  • [3] EZH2 regulates expression of FOXC1 by mediating H3K27me3 in breast cancers
    Zheng, Xiang-jin
    Li, Wan
    Yi, Jie
    Liu, Jin-yi
    Ren, Li-wen
    Zhu, Xiao-ming
    Liu, Shi-wei
    Wang, Jin-hua
    Du, Guan-hua
    ACTA PHARMACOLOGICA SINICA, 2021, 42 (07) : 1171 - 1179
  • [4] EZH2 -mediated H3K27me3 is a predictive biomarker and therapeutic target in uveal melanoma
    Hou, Chen
    Xiao, Lirong
    Ren, Xiang
    Cheng, Lin
    Guo, Bo
    Zhang, Meixia
    Yan, Naihong
    FRONTIERS IN GENETICS, 2022, 13
  • [5] Inhibition of Ezh2 In Vitro and the Decline of Ezh2 in Developing Midbrain Promote Dopaminergic Neurons Differentiation Through Modifying H3K27me3
    Hong, Feng
    Zhao, Mengxue
    Zhang, Lei
    Feng, Linyin
    STEM CELLS AND DEVELOPMENT, 2019, 28 (10) : 649 - 658
  • [6] The epigenetic EZH2/H3K27me3 axis modulates lactotroph tumor cell proliferation
    Zlocowski, N.
    Sosa, L. d, V
    De la Cruz-Thea, B.
    Guido, C. B.
    Martin, M. G.
    Mukdsi, J. H.
    Torres, A., I
    Petiti, J. P.
    JOURNAL OF ENDOCRINOLOGY, 2023, 257 (02)
  • [7] EZH2 Represses Target Genes through H3K27-Dependent and H3K27-Independent Mechanisms in Hepatocellular Carcinoma
    Gao, Shu-Bin
    Zheng, Qi-Fan
    Xu, Bin
    Pan, Chang-Bao
    Li, Kang-Li
    Zhao, Yue
    Zheng, Qi-Lin
    Lin, Xiao
    Xue, Li-Xiang
    Jin, Guang-Hui
    MOLECULAR CANCER RESEARCH, 2014, 12 (10) : 1388 - 1397
  • [8] EZH2 is a potential therapeutic target for H3K27M-mutant pediatric gliomas
    Mohammad, Faizaan
    Weissmann, Simon
    Leblanc, Benjamin
    Pandey, Deo P.
    Hojfeldt, Jonas W.
    Comet, Itys
    Zheng, Chunqin
    Johansen, Jens Vilstrup
    Rapin, Nicolas
    Porse, Bo T.
    Tvardovskiy, Andrey
    Jensen, Ole N.
    Olaciregui, Nagore G.
    Lavarino, Cinzia
    Sunol, Mariona
    de Torres, Carmen
    Mora, Jaume
    Carcaboso, Angel M.
    Helin, Kristian
    NATURE MEDICINE, 2017, 23 (04) : 483 - +
  • [9] A687V EZH2 Is a Driver of Histone H3 Lysine 27 ( H3K27) Hypertrimethylation
    Ott, Heidi M.
    Graves, Alan P.
    Pappalardi, Melissa B.
    Huddleston, Michael
    Halsey, Wendy S.
    Hughes, Ashley M.
    Groy, Arthur
    Dul, Edward
    Jiang, Yong
    Bai, Yuchen
    Annan, Roland
    Verma, Sharad K.
    Knight, Steven D.
    Kruger, Ryan G.
    Dhanak, Dashyant
    Schwartz, Benjamin
    Tummino, Peter J.
    Creasy, Caretha L.
    McCabe, Michael T.
    MOLECULAR CANCER THERAPEUTICS, 2014, 13 (12) : 3062 - 3073
  • [10] Evaluation of Histone 3 Lysine 27 Trimethylation (H3K27me3) and Enhancer of Zest 2 (EZH2) in Pediatric Glial and Glioneuronal Tumors Shows Decreased H3K27me3 in H3F3A K27M Mutant Glioblastomas
    Venneti, Sriram
    Garimella, Mihir T.
    Sullivan, Lisa M.
    Martinez, Daniel
    Huse, Jason T.
    Heguy, Adriana
    Santi, Mariarita
    Thompson, Craig B.
    Judkins, Alexander R.
    BRAIN PATHOLOGY, 2013, 23 (05) : 558 - 564