共 14 条
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.
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页码:501 / 510
页数:10
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