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

机译:镉抑制铁转运蛋白表达可刺激三阴性乳腺癌细胞增殖EMT和迁移

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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 μM 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-ß, 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.
机译:镉(Cd)与多种癌症有关,包括乳腺癌。然而,其致癌活性的分子机制尚不完全清楚。为此,本研究调查了铁转运蛋白(FPN)(一种乳腺癌的预后标志物)在Cd诱导的细胞增殖和细胞迁移刺激中的作用。用1-3μMCd处理三阴性MDA-MB-231细胞。细胞表现出FPN表达的显着降低和铁浓度的同时升高。 Cd处理8周的细胞显示出较高的增殖和迁移活性,与FPN表达成反比。 FPN表达降低也导致EMT,如E-钙粘蛋白表达增加,N-钙粘蛋白,Twist和Slug表达减少所表明。进一步的研究表明,Cd通过激活TPN-ß(一种已知的FPN表达调节剂)至少部分抑制了FPN表达。综上所述,这些结果表明,镉诱导的MDA-MB-231细胞增殖,EMT和迁移的刺激是通过抑制FPN表达和相关的铁稳态破坏而引起的。

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