Decreased Ferroportin Promotes Myeloma Cell Growth and Osteoclast Differentiation

被引:109
作者
Gu, Zhimin [1 ]
Wang, He [1 ]
Xia, Jiliang [1 ]
Yang, Ye [1 ]
Jin, Zhendong [2 ]
Xu, Hongwei [1 ]
Shi, Jumei [3 ]
De Domenico, Ivana [4 ]
Tricot, Guido [1 ]
Zhan, Fenghuang [1 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Pharm, Dept Pharmaceut Sci & Expt Therapeut, Iowa City, IA 52242 USA
[3] Tongji Univ, Sch Med, Dept Hematol, Shanghai Peoples Hosp 10, Shanghai 200092, Peoples R China
[4] Univ Utah, Dept Internal Med, Salt Lake City, UT 84112 USA
基金
中国国家自然科学基金;
关键词
MULTIPLE-MYELOMA; HEPCIDIN EXPRESSION; IRON HOMEOSTASIS; DRUG-RESISTANCE; CANCER; ACTIVATION; STAT3; INTERNALIZATION; METABOLISM; INDUCTION;
D O I
10.1158/0008-5472.CAN-14-3804
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Iron homeostasis is disrupted in multiple myeloma, a difficult-to-cure plasma cell malignancy with lytic bone lesions. Here, we systematically analyzed iron gene expression signature and demonstrated that mRNA expression of iron exporter ferroportin (FPN1) is significantly downregulated in myeloma cells and correlates negatively with clinic outcome. Restoring expression of FPN1 reduces intracellular liable iron pool, inhibits STAT3-MCL-1 signaling, and suppresses myeloma cells growth. Furthermore, we demonstrated that mRNA of FPN1 is also downregulated at the initial stages of osteoclast differentiation and suppresses myeloma cell-induced osteoclast differentiation through regulating iron regulator TFRC, NF-kappa B, and JNK pathways. Altogether, we demonstrated that down-regulation of FPN1 plays critical roles in promoting myeloma cell growth and bone resorption in multiple myeloma. (C) 2015 AACR.
引用
收藏
页码:2211 / 2221
页数:11
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