Epoxymicheliolide, a novelguaiane-type sesquiterpene lactone, inhibits NF-B/COX-2 signaling pathways by targeting leucine 281 and leucine 25 in IKK in renal cell carcinoma

被引:11
|
作者
Zhu, Jiabin [1 ,2 ]
Zhao, Jun [3 ]
Yu, Zhenlong [4 ]
Shrestha, Sandeep [1 ]
Song, Jing [5 ]
Liu, Wenwen [5 ]
Lan, Wen [5 ]
Xing, Jinshan [6 ]
Liu, Shuang [7 ]
Chen, Chen [8 ]
Cao, Momo [9 ]
Sun, Xiuzhen [10 ]
Wang, Qi [5 ]
Song, Xishuang [1 ]
机构
[1] Dalian Med Univ, Affiliated Hosp 1, Dept Urol, Dalian 116011, Liaoning, Peoples R China
[2] China Three Gorges Univ, Affiliated Renhe Hosp, Yichang 443000, Hubei, Peoples R China
[3] Dalian Med Univ, Affiliated Hosp 1, Dept Neurosurg, Dalian 116011, Liaoning, Peoples R China
[4] Dalian Med Univ, Coll Pharm, Dalian 116044, Liaoning, Peoples R China
[5] Dalian Med Univ, Dept Resp Med, Affiliated Hosp 2, Dalian 116023, Liaoning, Peoples R China
[6] Dalian Med Univ, Dept Neurosurg, Affiliated Hosp 2, Dalian 116023, Liaoning, Peoples R China
[7] Dalian Med Univ, Dept Gastroenterol, Affiliated Hosp 2, Dalian 116023, Liaoning, Peoples R China
[8] Dalian Med Univ, Affiliated Hosp 1, Dept Cardiovasc Med, Dalian 116011, Liaoning, Peoples R China
[9] Dalian Med Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Dalian 116011, Liaoning, Peoples R China
[10] Dalian Med Univ, Affiliated Hosp 2, Dept Otorhinolaryngol, Dalian 116023, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
epoxymicheliolide; renal cell carcinoma; nuclear factor-B; inhibitor of NF-B kinase; cyclooxygenase-2; NF-KAPPA-B; CANCER; PARTHENOLIDE; ACTIVATION; EXPRESSION; SUPPRESSION; INFLAMMATION; MECHANISMS; PREVENTION; APOPTOSIS;
D O I
10.3892/ijo.2018.4460
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Parthenolide (PTL) is a sesquiterpene lactone compound obtained from Tanacetum parthenium (feverfew) and inhibits the activation of nuclear factor (NF)-B. Epoxymicheliolide (EMCL) is a compound which is structurally related to PTL; however, EMCL is more stable under acidic and alkaline conditions. As a biologically active molecule, the detailed mechanism by which EMCL inhibits tumor activity remains to be elucidated. The present study evaluated the effect of EMCL on renal cell carcinoma (RCC) cells and identified the underlying mechanisms. It was found that treatment with EMCL significantly inhibited the proliferation of RCC cells in vitro and increased the induction of apoptosis by activating the mitochondria- and caspase-dependent pathway. Simultaneously, EMCL suppressed cell invasion and metastasis by inhibiting epithelial-mesenchymal transition, as observed in a microfluidic chip assay. Furthermore, using immunofluorescence analysis, an electrophoretic mobility shift assay and a dual-luciferase reporter assay, it was shown that treatment with EMCL significantly suppressed the expression of cyclooxygenase-2 by inhibiting the translocation of NF-B p50/p65 and the activity of NF-B. Collectively, the results indicated that EMCL suppressed tumor growth by inhibiting the activation of NF-B and suggested that EMCL may be a novel anticancer agent in the treatment of RCC.
引用
收藏
页码:987 / 1000
页数:14
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