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Targeting the cross-talk between the hedgehog and NF-κB signaling pathways in multiple myeloma
被引:16
|作者:
Cai, Ke
[1
]
Na, Wenxiu
[1
]
Guo, Mengjie
[2
]
Xu, Ruirong
[1
]
Wang, Xinfeng
[1
]
Qin, Yi
[1
]
Wu, Yan
[1
]
Jiang, Jie
[1
]
Huang, Hongming
[1
]
机构:
[1] Nantong Univ, Affiliated Hosp, Dept Hematol, 20 Xisi Rd, Nantong 226001, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Sch Med & Life Sci, Nanjing 210023, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Multiple myeloma;
Hedgehog;
NF-kappa B;
SMO;
GLI1;
SONIC HEDGEHOG;
CANCER CELLS;
ACTIVATION;
PROTEINS;
GENE;
D O I:
10.1080/10428194.2018.1493727
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Multiple myeloma (MM) is an incurable plasma cell malignancy. Aberrant activation of the Hedgehog (Hh) and NF-kappa B signaling pathways is observed in MM and plays a pivotal role in the development of MM by promoting myeloma cell growth, survival, and drug resistance. In this study, we found that the Sonic Hh (SHh) ligand in the bone marrow microenvironment is responsible for the enhancement of NF-kappa B activity in MM cell lines NCI-H929 and U266. Notably, we discovered that Hh signaling regulates NF-kappa B through its classical pathway (SHh/PTCH1/SMO/GLI1) in MM cells. Meanwhile, non-classical pathway by SMO recruitment of TRAF6 to ubiquitination is also involved in it. Moreover, the SMO inhibitor cyclopamine enhances the cytotoxic effects of bortezomib in MM cell lines. Our study reveals the cross-talk between Hh members and the NF-kappa B pathway in the myeloma cells and provides a theoretical basis for combined utilization of Hh members and proteasome inhibition in MM.
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页码:772 / 781
页数:10
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