Identification of a derivative of the alkaloid emetine as an inhibitor of the YAP-TEAD interaction and its potential as an anticancer agent

被引:1
|
作者
Sekine, Saaya [1 ,2 ]
Takase, Shohei [1 ]
Hayase, Runa [1 ]
Noritsugu, Kota [1 ]
Maemoto, Yuki [1 ]
Ichikawa, Yasue [3 ]
Ogawa, Kenji [3 ,4 ]
Kondoh, Yasumitsu [5 ]
Osada, Hiroyuki [5 ,6 ]
Yoshida, Minoru [2 ,3 ,7 ]
Ito, Akihiro [1 ,2 ]
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Life Sci, Lab Cell Signaling, Hachioji, Tokyo, Japan
[2] RIKEN Ctr Sustainable Resource Sci, Chem Genom Res Grp, Wako, Saitama, Japan
[3] RIKEN Ctr Sustainable Resource Sci, Drug Discovery Seed Cpds Exploratory Unit, Wako, Saitama, Japan
[4] Nihon Univ, Coll Bioresource Sci, Lab Vet Epizootiol, Fujisawa, Kanagawa, Japan
[5] RIKEN Ctr Sustainable Resource Sci, Chem Resource Dev Res Unit, Wako, Saitama, Japan
[6] Univ Shizuoka, Dept Pharmaceut Sci, Suruga Ku, Shizuoka, Japan
[7] Univ Tokyo, Dept Biotechnol, Bunkyo Ku, Tokyo, Japan
基金
日本学术振兴会;
关键词
YAP; TEAD; Hippo pathway; emetine; anticancer agent; HIPPO PATHWAY; PROTEIN INTERACTIONS; CELL-PROLIFERATION; YAP/TAZ; METHYLATION; STABILITY; APOPTOSIS;
D O I
10.1093/bbb/zbad022
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
TEAD is a transcription factor responsible for the output of the tumor suppressor Hippo pathway. The transcriptional activity of TEAD requires molecular interaction with its transcriptional coactivator, YAP. Aberrant activation of TEAD is deeply involved in tumorigenesis and is associated with poor prognosis, suggesting that inhibitors targeting the YAP-TEAD system are promising as antitumor agents. In this study, we identified NPD689, an analog of the natural product alkaloid emetine, as an inhibitor of the YAP-TEAD interaction. NPD689 suppressed the transcriptional activity of TEAD and reduced the viability of human malignant pleural mesothelioma and non-small cell lung cancer cells but not the viability of normal human mesothelial cells. Our results suggest that NPD689 is not only a new useful chemical tool for elucidating the biological role of the YAP-TEAD system but also has potential as a starting compound for developing a cancer therapeutic agent that targets the YAP-TEAD interaction.
引用
收藏
页码:501 / 510
页数:10
相关论文
共 14 条
  • [1] Identification of Celastrol as a Novel YAP-TEAD Inhibitor for Cancer Therapy by High Throughput Screening with Ultrasensitive YAP/TAZ-TEAD Biosensors
    Nouri, Kazem
    Azad, Taha
    Ling, Min
    van Rensburg, Helena J. Janse
    Pipchuk, Alexander
    Shen, He
    Hao, Yawei
    Zhang, Jianmin
    Yang, Xiaolong
    CANCERS, 2019, 11 (10)
  • [2] A high-affinity Optide (optimized peptide) inhibitor of the Hippo pathway's YAP-TEAD interaction
    Crook, Zachary R.
    Bradley, Philip
    Sevilla, Gregory
    Friend, Della
    King, Chris
    Mhyre, Andrew
    Strong, Roland
    Baker, David
    Olson, James M.
    CANCER RESEARCH, 2017, 77
  • [3] Antiproliferative and Antimigratory Effects of a Novel YAP-TEAD Interaction Inhibitor Identified Using in Silico Molecular Docking
    Smith, Sarah A.
    Sessions, Richard B.
    Shoemark, Deborah K.
    Williams, Christopher
    Ebrahimighaei, Reza
    McNeill, Madeleine C.
    Crump, Matthew P.
    McKay, Tristan R.
    Harris, Gemma
    Newby, Andrew C.
    Bond, Mark
    JOURNAL OF MEDICINAL CHEMISTRY, 2019, 62 (03) : 1291 - 1305
  • [4] Identification of small molecule Pan-TEAD inhibitors disrupting YAP-TEAD protein-protein interaction and targeting gastric cancer cells
    Kumar, Ramesh
    Toh, Joel
    Thian, Joanne
    Mohideen, Noorul Farzana
    Sun, Jialin
    Chakraborty, Sayan
    Gunaratne, Jayantha
    Hong, Wanjin
    CANCER RESEARCH, 2024, 84 (07)
  • [5] Hot Spot Analysis of YAP-TEAD Protein-Protein Interaction Using the Fragment Molecular Orbital Method and Its Application for Inhibitor Discovery
    Kim, Jongwan
    Lim, Hocheol
    Moon, Sungho
    Cho, Seon Yeon
    Kim, Minhye
    Park, Jae Hyung
    Park, Hyun Woo
    No, Kyoung Tai
    CANCERS, 2021, 13 (16)
  • [6] IDENTIFICATION OF A NOVEL YAP: TEAD INTERACTION INHIBITOR THAT DIFFERENTIALLY REGULATES PROLIFERATION AND MIGRATION IN VSMCS AND ECS
    Smith, Sarah
    Sessions, Richard B.
    Schoemark, Deborah
    Williams, Christopher
    Smith, Madeleine
    Crump, Matthew
    Newby, Andrew
    Bond, Mark
    CARDIOVASCULAR RESEARCH, 2018, 114 : S9 - S9
  • [7] A novel cyclic peptide inhibitor targeting the YAP-TEAD protein-protein interaction shows potent anti-tumor effect in a variety of human malignancies including mesothelioma
    Hu, Yi P.
    Wang, Yinghua M.
    Lee, Daniel
    Ren, Yi
    CANCER RESEARCH, 2020, 80 (16)
  • [8] Synthesis of naphthazarin derivatives and identification of novel thioredoxin reductase inhibitor as potential anticancer agent
    Zhang, Junmin
    Liu, Yaping
    Shi, Danfeng
    Hu, Guodong
    Zhang, Baoxin
    Li, Xinming
    Liu, Ruijuan
    Han, Xiao
    Yao, Xiaojun
    Fang, Jianguo
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 140 : 435 - 447
  • [9] In vitro and in vivo characterization of a benzofuran derivative, a potential anticancer agent, as a novel Aurora B kinase inhibitor
    Xie, Fang
    Zhu, Hengrui
    Zhang, Haoxing
    Lang, Qingyu
    Tang, Lisha
    Huang, Qiang
    Yu, Long
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2015, 89 : 310 - 319
  • [10] Identification of Flavone Derivative Displaying a 4′-Aminophenoxy Moiety as Potential Selective Anticancer Agent in NSCLC Tumor Cells
    Mobbili, Giovanna
    Romaldi, Brenda
    Sabbatini, Giulia
    Amici, Adolfo
    Marcaccio, Massimo
    Galeazzi, Roberta
    Laudadio, Emiliano
    Armeni, Tatiana
    Minnelli, Cristina
    MOLECULES, 2023, 28 (07):