RETRACTED: Hispidulin suppresses cell growth and metastasis by targeting PIM1 through JAK2/STAT3 signaling in colorectal cancer (Retracted article. See vol. 111, pg. 2196, 2020)

被引:71
|
作者
Liu, Kaili [1 ]
Gao, Hui [1 ]
Wang, Qiaoyun [2 ]
Wang, Longyuan [2 ]
Zhang, Bin [2 ]
Han, Zhiwu [2 ]
Chen, Xuehong [3 ]
Han, Mei [1 ]
Gao, Mingquan [1 ]
机构
[1] Qingdao Univ, Sch Pharm, Dept Pharmacol, Qingdao, Peoples R China
[2] Qingdao Univ, Dept Pharm, Affiliated Hosp, Qingdao, Peoples R China
[3] Qingdao Univ, Coll Med, Qingdao, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; hispidulin; PIM1; ROS; STAT3; KINASE INHIBITION; CYCLE PROGRESSION; CARCINOMA; APOPTOSIS; PROLIFERATION; EXPRESSION; MYC; DIFFERENTIATION; FLAVONOIDS; INVASION;
D O I
10.1111/cas.13575
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) accounts for over 600000 deaths annually worldwide. The current study aims to evaluate the value of proto-oncogene PIM1 as a therapeutic target in CRC and investigate the anticancer activity of hispidulin, a naturally occurring phenolic flavonoid compound, against CRC. Immunohistochemistry analysis showed that PIM1 was upregulated in CRC tissue. The role of PIM1 as an oncogene was evidenced by the fact that PIM1 knockdown inhibits cell growth, induces apoptosis, and suppresses invasion. Our results showed that hispidulin exerts antitumor activity in CRC through inhibiting the expression of PIM1. Moreover, our findings revealed that hispidulin downregulated the expression of PIM1 by inhibiting JAK2/STAT3 signaling by generating reactive oxygen species. Furthermore, our invivo studies showed that hispidulin can significantly inhibit tumor growth and metastasis in CRC. Collectively, our results provide an experimental basis for trialing hispidulin in CRC treatment. PIM1 can be considered a potential therapeutic target in CRC.
引用
收藏
页码:1369 / 1381
页数:13
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