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Se(2)Mo(10)V(3), a heteropoly compound containing selenium, inhibits tumor growth

Selenium compounds have strong anti-tumor effects and are well-tolerated. We examined the anti-tumor effects of (NH(4))(2)H(15)Se(2)(VI)Mo(10)V(3)O(52)·2H(2)O (Se(2)Mo(10)V(3)), a heteropoly compound containing selenium. Se(2)Mo(10)V(3) inhibited proliferation in K562 cells with a half-maximal inhib...

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Detalles Bibliográficos
Autores principales: Zhang, Hong-Ning, Feng, Wei-Li, An, Chun-Na, Li, Wen-Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620220/
https://www.ncbi.nlm.nih.gov/pubmed/28978080
http://dx.doi.org/10.18632/oncotarget.18909
Descripción
Sumario:Selenium compounds have strong anti-tumor effects and are well-tolerated. We examined the anti-tumor effects of (NH(4))(2)H(15)Se(2)(VI)Mo(10)V(3)O(52)·2H(2)O (Se(2)Mo(10)V(3)), a heteropoly compound containing selenium. Se(2)Mo(10)V(3) inhibited proliferation in K562 cells with a half-maximal inhibitory concentration of 78.72±2.82 mg/L after 48 h and 24.94±0.88 mg/L after 72 h. Typical apoptotic morphologies were also observed in K562 cells treated with Se(2)Mo(10)V(3), as were increased intracellular levels of Ca(2+), Mg(2+), H(+), and reactive oxygen species, and decreased mitochondrial membrane potential. In addition, Se(2)Mo(10)V(3) treatment triggered cytochrome C release and inhibited IκBα degradation and NF-κB translocation. In vivo experiments revealed that 5 or 10 mg/kg Se(2)Mo(10)V(3) inhibited the growth of sarcoma 180 and hepatoma 22 xenograft tumors. These results indicate that Se(2)Mo(10)V(3) inhibits tumor growth both in vitro and in vivo and induces apoptosis in K562 cells, possibly by inhibiting the NF-κB/IκBα pathway.