Suppression of ferroportin expression by cadmium stimulates proliferation, EM, and migration in triple-negative breast cancer cells

被引:43
|
作者
Shan, Zhongguo [1 ]
Wei, Zhengxi [1 ,2 ]
Shaikh, Zahir A. [1 ]
机构
[1] Univ Rhode Isl, Coll Pharm, Ctr Mol Toxicol, Dept Biomed & Pharmaceut Sci, Kingston, RI 02881 USA
[2] NIH, Div Preclin Innovat, Natl Ctr Advancing Translat Sci, 9800 Med Ctr Dr, Rockville, MD 20850 USA
关键词
Cadmium; Iron; Ferroportin; Breast cancer; EMT; ER-ALPHA; IRON; EXPOSURE; GROWTH; METASTASIS; PROMOTES; HEPCIDIN; ACTIVATION; MECHANISMS; BIOMARKERS;
D O I
10.1016/j.taap.2018.07.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cadmium (Cd) has been linked to a variety of cancers, including breast cancer; however, the molecular mechanism of its carcinogenic activity is not fully understood. To this end, the present study investigated the roles of ferroportin (FPN), a prognostic marker of breast cancer, in Cd-induced stimulation of cell proliferation and cell migration. Triple-negative MDA-MB-231 cells were treated with 1-3 mu M Cd. The cells exhibited significant reduction in FPN expression and concomitant increase in iron concentration. Cells treated with Cd for 8 weeks displayed elevated proliferative and migratory activities which were inversely related with FPN expression. Reduced FPN expression also resulted in EMT as indicated by an increase in the expression of E-cadherin, and a decrease in the expression of N-cadherin, Twist and Slug. Further investigation revealed that Cd suppressed FPN expression at least partially by activating TGF-beta, a known regulator of FPN expression. Taken together, these results indicate that Cd-induced stimulation of MDA-MB-231 cell proliferation, EMT, and migration is brought about by suppression of FPN expression and associated disruption of iron homeostasis.
引用
收藏
页码:36 / 43
页数:8
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