Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy

被引:20
作者
Li, Rui [1 ,2 ]
Zhou, Yue [1 ,2 ]
Zhang, Xinxin [1 ,2 ]
Yang, Lujia [1 ,2 ]
Liu, Jieyu [1 ,2 ]
Wightman, Samantha M. [3 ]
Lv, Ling [1 ,2 ]
Liu, Zhiqing [1 ,2 ]
Wang, Chang-Yun [1 ,2 ]
Zhao, Chenyang [1 ,2 ]
机构
[1] Ocean Univ China, Inst Evolut & Marine Biodivers, Coll Food Sci & Engn, Sch Med, Qingdao 266003, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao 266237, Peoples R China
[3] Cleveland Clin, Lerner Res Inst, Dept Canc Biol, Cleveland, OH 44195 USA
基金
中国国家自然科学基金;
关键词
Pretrichodermamide B; Signal transducer and activator of transcription 3 (STAT3); Marine natural products; Target protein; In vivo anti-cancer efficacy; CANCER; SIGNALS;
D O I
10.1007/s42995-022-00162-x
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
The Janus kinase (JAK)/signal transducer and activator of transcription 3 (STAT3) regulates the expression of various critical mediators of cancer and is considered as one of the central communication nodes in cell growth and survival. Marine natural products (MNP) represent great resources for discovery of bioactive lead compounds, especially anti-cancer agents. Through the medium-throughput screening of our in-house MNP library, Pretrichodermamide B, an epidithiodiketopiperazine, was identified as a JAK/STAT3 signaling inhibitor. Further studies identified that Pretrichodermamide B directly binds to STAT3, preventing phosphorylation and thus inhibiting JAK/STAT3 signaling. Moreover, it suppressed cancer cell growth, in vitro, at low micromolar concentrations and demonstrated efficacy in vivo by decreasing tumor growth in a xenograft mouse model. In addition, it was shown that Pretrichodermamide B was able to induce cell cycle arrest and promote cell apoptosis. This study demonstrated that Pretrichodermamide B is a novel STAT3 inhibitor, which should be considered for further exploration as a promising anti-cancer therapy.
引用
收藏
页码:94 / 101
页数:8
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