Nobiletin, a citrus polymethoxyflavone, enhances the effects of bicalutamide on prostate cancer cells via down regulation of NF-κB, STAT3, and ERK activation

被引:17
作者
Ma, Yuran [1 ]
Ren, Xiang [1 ]
Patel, Nandini [2 ]
Xu, Xuetao [1 ,3 ]
Wu, Panpan [1 ]
Liu, Wenfeng [1 ,3 ]
Zhang, Kun [1 ,3 ]
Goodin, Susan [4 ]
Li, Dongli [1 ,3 ]
Zheng, Xi [2 ,4 ]
机构
[1] Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen 529020, Guangdong, Peoples R China
[2] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Chem Biol, 164 Frelinghuysen Rd, Piscataway, NJ 08854 USA
[3] Int Healthcare Innovat Inst Jiangmen, Jiangmen 529020, Guangdong, Peoples R China
[4] Rutgers Canc Inst New Jersey, New Brunswick, NJ 08903 USA
关键词
SIGNALING PATHWAYS; COMBINATION; PROLIFERATION; INFLAMMATION; MECHANISMS; RESISTANCE; DOCETAXEL; APOPTOSIS;
D O I
10.1039/c9ra10020b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Natural products have shown potential to be combined with current cancer therapies to improve patient outcomes. Nobiletin (NBT) is a citrus polymethoxyflavone and has been shown to exert an anticancer effect in various cancer cells. We investigated the effects and mechanisms of NBT in combination with bicalutamide (BCT), a commonly used anti-androgen drug in prostate cancer therapy, on prostate cancer cells. Our results demonstrate that the combined treatment with NBT and BCT produces an enhanced inhibitory effect on the growth of prostate cancer cells compared to either compound alone. The synergistic action of NBT and BCT was confirmed using isobologram analysis. Moreover, this study has shown that NBT and BCT synergistically inhibited colony formation and migration as well as induced apoptosis. Mechanistic studies demonstrate that NBT and BCT combination reduced key cellular signaling regulators including: p-Erk/Erk, p-STAT3/STAT3 and NF-kappa B. Overall, these results suggest that NBT combination with BCT may be an effective treatment for prostate cancer.
引用
收藏
页码:10254 / 10262
页数:9
相关论文
共 45 条
[1]  
[Anonymous], CANCERS
[2]  
[Anonymous], 2019, Cancers (Basel)
[3]   Nobiletin suppresses cell viability through AKT Pathways in PC-3 and DU-145 prostate cancer cells [J].
Chen, Jianchu ;
Creed, Ashley ;
Chen, Allen Y. ;
Huang, Haizhi ;
Li, Zhaoliang ;
Rankin, Gary O. ;
Ye, Xingqian ;
Xu, Guihua ;
Chen, Yi Charlie .
BMC PHARMACOLOGY & TOXICOLOGY, 2014, 15 :59
[4]   Nobiletin Down-Regulates c-KIT Gene Expression and Exerts Antileukemic Effects on Human Acute Myeloid Leukemia Cells [J].
Chen, Pei-Yi ;
Chen, Yu-Ting ;
Gao, Wan-Yun ;
Wu, Ming-Jiuan ;
Yen, Jui-Hung .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2018, 66 (51) :13423-13434
[5]   Nobiletin inhibits human osteosarcoma cells metastasis by blocking ERK and JNK-mediated MMPs expression [J].
Cheng, Hsin-Lin ;
Hsieh, Ming-Ju ;
Yang, Jia-Sin ;
Lin, Chiao-Wen ;
Lue, Ko-Haung ;
Lu, Ko-Hsiu ;
Yang, Shun-Fa .
ONCOTARGET, 2016, 7 (23) :35208-35223
[6]   Drug Combination Studies and Their Synergy Quantification Using the Chou-Talalay Method [J].
Chou, Ting-Chao .
CANCER RESEARCH, 2010, 70 (02) :440-446
[7]   Bicalutamide failure in prostate cancer treatment: Involvement of Multi Drug Resistance proteins [J].
Colabufo, Nicola Antonio ;
Pagliarulo, Vincenzo ;
Berardi, Francesco ;
Contino, Marialessandra ;
Inglese, Carmela ;
Niso, Mauro ;
Ancona, Patrizia ;
Albo, Giancarlo ;
Pagliarulo, Arcangelo ;
Perrone, Roberto .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2008, 601 (1-3) :38-42
[8]   Androgen Receptor Targeted Treatments of Prostate Cancer: 35 Years of Progress with Antiandrogens [J].
Crawford, E. David ;
Schellhammer, Paul F. ;
McLeod, David G. ;
Moul, Judd W. ;
Higano, Celestia S. ;
Shore, Neal ;
Denis, Louis ;
Iversen, Peter ;
Eisenberger, Mario A. ;
Labrie, Fernand .
JOURNAL OF UROLOGY, 2018, 200 (05) :956-966
[9]   Synergistic Effects of Nobiletin and Sorafenib Combination on Metastatic Prostate Cancer Cells [J].
Eskiler, Gamze Guney ;
Deveci, Asuman Ozkan ;
Bilir, Cemil ;
Kaleli, Suleyman .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2019, 71 (08) :1299-1312
[10]   NF-κB and STAT3 signaling pathways collaboratively link inflammation to cancer [J].
Fan, Yihui ;
Mao, Renfang ;
Yang, Jianhua .
PROTEIN & CELL, 2013, 4 (03) :176-185