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IMB5036 inhibits human pancreatic cancer growth primarily through activating necroptosis
被引:10
|作者:
Zhao, Qi
[1
,2
]
Zheng, Yanbo
[2
]
Lv, Xing
[3
]
Gong, Jianhua
[2
]
Yang, Lijun
[1
]
机构:
[1] Shanxi Med Univ, Minist Educ, Key Lab Cellular Physiol, Dept Pharmacol, Taiyuan 030001, Shanxi, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Biotechnol, Dept Oncol, Beijing 100050, Peoples R China
[3] Shanxi Med Univ, Minist Educ, Key Lab Cellular Physiol, Dept Biochem & Mol Biol, Taiyuan, Peoples R China
基金:
中国国家自然科学基金;
关键词:
cell death;
MLKL;
necroptosis;
pancreatic cancer;
pyridazinone;
MIXED LINEAGE KINASE;
DOMAIN-LIKE PROTEIN;
MOLECULAR-MECHANISMS;
CELL-DEATH;
APOPTOSIS;
GEMCITABINE;
SURVIVAL;
THERAPY;
D O I:
10.1111/bcpt.13694
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
IMB5036 is a novel pyridazinone compound with potent cytotoxicity. In this study, we reported its antitumour activity against pancreatic cancer and the underlying mechanism. We found that IMB5036 induced rapid cell swelling and increased membrane permeability in pancreatic cancer cells. IMB5036 increased the ratio of PI+ cells, which could be rescued by necroptosis inhibitor. Furthermore, MLKL inhibitor NSA attenuated the killing effect of IMB5036 on pancreatic cancer cells. IMB5036 stimulated translocation of MLKL and p-MLKL from cytoplasm to cell membrane. IMB5036 upregulated the level of p-RIPK1, p-RIPK3, and p-MLKL. At the same time, IMB5036 also partially activated apoptosis and pyroptosis. IMB5036 inhibited tumour growth in pancreatic xenograft. IMB5036 induced larger necrosis area, increased p-MLKL level, and inhibited Ki67 expression in tumour mass. The study indicates that IMB5036 inhibits human pancreatic cancer growth primarily activating necroptosis.
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页码:375 / 384
页数:10
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