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:16
|
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 50 条
  • [21] Gramine attenuates EGFR-mediated inflammation and cell proliferation in oral carcinogenesis via regulation of NF-κB and STAT3 signaling
    Ramu, Arunkumar
    Kathiresan, Suresh
    Ramadoss, Hemavardhini
    Nallu, Anandhi
    Kaliyan, Ramachandran
    Azamuthu, Theerthu
    BIOMEDICINE & PHARMACOTHERAPY, 2018, 98 : 523 - 530
  • [22] Calycosin Induces Gastric Cancer Cell Apoptosis via the ROS-Mediated MAPK/STAT3/NF-κB Pathway
    Zhang, Yu
    Zhang, Jian-Qiang
    Zhang, Tong
    Xue, Hui
    Zuo, Wen-Bo
    Li, Yan-Nan
    Zhao, Yue
    Sun, Geng
    Fu, Zhong-Ren
    Zhang, Qing
    Zhao, Xue
    Teng, Yue
    Wang, An-Qi
    Li, Jia-Zhu
    Wang, Ying
    Jin, Cheng-Hao
    ONCOTARGETS AND THERAPY, 2021, 14 : 2505 - 2517
  • [23] Baicalin reduces inflammation to inhibit lung cancer via targeting SOCS1/NF- κ B/STAT3 axis
    Guo, Lijuan
    Yue, Ming
    Ma, Chengyuan
    Wang, Yunjing
    Hou, Jiejie
    Li, Hong
    HELIYON, 2024, 10 (08)
  • [24] Sugiol inhibits STAT3 activity via regulation of transketolase and ROS-mediated ERK activation in DU145 prostate carcinoma cells
    Jung, Seung-Nam
    Shin, Dae-Seop
    Kim, Hye-Nan
    Jeon, Yoon Jung
    Yun, Jieun
    Lee, Yu-Jin
    Kang, Jong Soon
    Han, Dong Cho
    Kwon, Byoung-Mog
    BIOCHEMICAL PHARMACOLOGY, 2015, 97 (01) : 38 - 50
  • [25] Propapoptotic effects of NF-κB in LNCaP prostate cancer cells lead to serine protease activation
    Kimura, K
    Gelmann, E
    CELL DEATH AND DIFFERENTIATION, 2002, 9 (09) : 972 - 980
  • [26] Propapoptotic effects of NF-κB in LNCaP prostate cancer cells lead to serine protease activation
    K Kimura
    E P Gelmann
    Cell Death & Differentiation, 2002, 9 : 972 - 980
  • [27] TLR9 signaling through NF-κB/RELA and STAT3 promotes tumor-propagating potential of prostate cancer cells
    Moreira, Dayson
    Zhang, Qifang
    Hossain, Dewan Md S.
    Nechaev, Sergey
    Li, Haiqing
    Kowolik, Claudia M.
    D'Apuzzo, Massimo
    Forman, Stephen
    Jones, Jeremy
    Pal, Sumanta K.
    Kortylewski, Marcin
    ONCOTARGET, 2015, 6 (19) : 17302 - 17313
  • [28] Rig-G is a growth inhibitory factor of lung cancer cells that suppresses STAT3 and NF-κB
    Li, Dong
    Sun, Junjun
    Liu, Wenfang
    Wang, Xuan
    Bals, Robert
    Wu, Junlu
    Quan, Wenqiang
    Yao, Yiwen
    Zhang, Yu
    Zhou, Hong
    Wu, Kaiyin
    ONCOTARGET, 2016, 7 (40) : 66032 - 66050
  • [29] Tetrandrine suppresses -glucan-induced macrophage activation via inhibiting NF-B, ERK and STAT3 signaling pathways
    Xu, Jing
    Liu, Dabiao
    Yin, Qing
    Guo, Lanfang
    MOLECULAR MEDICINE REPORTS, 2016, 13 (06) : 5177 - 5184
  • [30] The gold compound auranofin induces apoptosis of human multiple myeloma cells through both down-regulation of STAT3 and inhibition of NF-κB activity
    Nakaya, Aya
    Sagawa, Morihiko
    Muto, Akihiro
    Uchida, Hideo
    Ikeda, Yasuo
    Kizaki, Masahiro
    LEUKEMIA RESEARCH, 2011, 35 (02) : 243 - 249