Inactivation of transforming growth factor-β-activated kinase 1 promotes taxol efficacy in ovarian cancer cells

被引:5
作者
Bo, Li [1 ,2 ]
Cui, Huchuan [3 ]
Fang, Zhengxian [2 ]
Qun, Tao [2 ]
Xia, Caoyun [1 ]
机构
[1] Anhui Med Univ, Dept Obstet & Gynaecol, 81 Meishan Rd, Hefei 230032, Peoples R China
[2] Anhui Med Univ, Chaohu Hosp, Dept Obstet & Gynaecol, Chaohu 238000, Peoples R China
[3] Anhui Med Univ, Chaohu Hosp, Clin Lab, Chaohu 238000, Peoples R China
关键词
TAK1; Taxol; Ovarian cancer; 5Z-7-oxozeaenol; KAPPA-B ACTIVATION; PACLITAXEL RESISTANCE; TAK1; TUBULIN; CHEMOTHERAPY; RELAPSE; PROTEIN; AGENTS; JNK; DNA;
D O I
10.1016/j.biopha.2016.09.105
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Resistance to taxol represents a major obstacle for long-term remission in ovarian cancer. Transforming Growth Factor-beta-Activated Kinase 1 (TAK1) is a critical component in immune response pathway. However, the role of TAK1 in the development of chemoresistance in ovarian cancer remains unknown. Here, we showed that in vitro, taxol-resistant cells expressed higher TAK1, and the ratio of p-TAK1/TAK1 positively associated with taxol resistance in ovarian cancer cells. Inactivation of TAK1 by inhibitor 5Z-7-oxozeaenol or gene knockdown sensitized taxol cytotoxicity in vitro, promoting cell apoptosis and mitosis arrest. Moreover, resistant cells were much more sensitive to the combined TAK1 inhibitor and taxol treatment than their parental counterparts. Using xenograft mouse model, we found that 5Z-7-oxozeaenol significantly enhanced taxol efficacy in vivo. Thus, targeting TAK1 pathway is a promising strategy to enhance taxol response in ovarian cancer treatment. (C) 2016 Published by Elsevier Masson SAS.
引用
收藏
页码:917 / 924
页数:8
相关论文
共 30 条
[1]   Cell type-specific function of TAK1 in innate immune signaling [J].
Ajibade, Adebusola A. ;
Wang, Helen Y. ;
Wang, Rong-Fu .
TRENDS IN IMMUNOLOGY, 2013, 34 (07) :307-316
[2]   Mapping the Functional Binding Sites of Cholesterol in β2-Adrenergic Receptor by Long-Time Molecular Dynamics Simulations [J].
Cang, Xiaohui ;
Du, Yun ;
Mao, Yanyan ;
Wang, Yuanyuan ;
Yang, Huaiyu ;
Jiang, Hualiang .
JOURNAL OF PHYSICAL CHEMISTRY B, 2013, 117 (04) :1085-1094
[3]   Molecular determinants of chemotherapy resistance in ovarian cancer [J].
Cooley, Megan ;
Fang, Pingping ;
Fang, Fang ;
Nephew, Kenneth P. ;
Chien, Jeremy .
PHARMACOGENOMICS, 2015, 16 (16) :1763-1767
[4]   Acquisition of paclitaxel resistance via PI3K-dependent epithelial-mesenchymal transition in A2780 human ovarian cancer cells [J].
Du, Fangfang ;
Wu, Xiaohong ;
Liu, Yanjun ;
Wang, Teng ;
Qi, Xiaowei ;
Mao, Yong ;
Jiang, Li ;
Zhu, Yifei ;
Chen, Yun ;
Zhu, Ruiyu ;
Han, Xiaofeng ;
Jin, Jian ;
Ma, Xin ;
Hua, Dong .
ONCOLOGY REPORTS, 2013, 30 (03) :1113-1118
[5]   TGF-β1 Induced Transdifferentiation of RPE Cells is Mediated by TAK1 [J].
Dvashi, Zeev ;
Goldberg, Mordechai ;
Adir, Orit ;
Shapira, Michal ;
Pollack, Ayala .
PLOS ONE, 2015, 10 (04)
[6]   Hypoxia suppresses cylindromatosis (CYLD) expression to promote inflammation in glioblastoma: possible link to acquired resistance to anti-VEGF therapy [J].
Guo, Jianying ;
Shinriki, Satoru ;
Su, Yu ;
Nakamura, Takuya ;
Hayashi, Mitsuhiro ;
Tsuda, Yukimoto ;
Murakami, Yoshitaka ;
Tasaki, Masayoshi ;
Hide, Takuichiro ;
Takezaki, Tatsuya ;
Kuratsu, Jun-ichi ;
Yamashita, Satoshi ;
Ueda, Mitsuharu ;
Li, Jian-Dong ;
Ando, Yukio ;
Jono, Hirofumi .
ONCOTARGET, 2014, 5 (15) :6353-6364
[7]   The activation of c-Jun NH2-terminal kinase (JNK) by DNA-damaging agents serves to promote drug resistance via activating transcription factor 2 (ATF2)-dependent enhanced DNA repair [J].
Hayakawa, J ;
Depatie, C ;
Ohmichi, M ;
Mercola, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (23) :20582-20592
[8]   TLR4-MyD88-TRAF6-TAK1 Complex-Mediated NF-κB Activation Contribute to the Anti-Inflammatory Effect of V8 in LPS-Induced Human Cervical Cancer SiHa Cells [J].
He, Aiqin ;
Ji, Rui ;
Shao, Jia ;
He, Chenyun ;
Jin, Ming ;
Xu, Yunzhao .
INFLAMMATION, 2016, 39 (01) :172-181
[9]   OVARIAN CANCER: BEYOND RESISTANCE [J].
Holmes, David .
NATURE, 2015, 527 (7579) :S217-S217
[10]   Identifying patients unlikely to benefit from further chemotherapy: A descriptive study of outcome at each relapse in ovarian cancer [J].
Hoskins, PJ ;
Le, N .
GYNECOLOGIC ONCOLOGY, 2005, 97 (03) :862-869