Nanohydroxyapatite exerts antitumor effects by preventing cellular proliferation and migration in glioma cells

Hydroxyapatite (Ca10(PO4)6(OH)2; HAP) is an essential component of the human bone inorganic phase. At the nanoscale level, nano-HAP (nHAP) presents marked emergent properties differing substantially from those of the bulk counterpart. Interestingly, these properties depend on nanoparticle characteri...

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Detalles Bibliográficos
Autor principal: Gorojod, Roxana Mayra
Otros Autores: Porte Alcon, Soledad, Dittler, María Laura, Gonzalez, Mónica Cristina, Kotler, Mónica L.
Formato: Artículo
Lenguaje:Inglés
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Acceso en línea:10.1093/toxsci/kfz019
Aporte de:Registro referencial: Solicitar el recurso aquí
Descripción
Sumario:Hydroxyapatite (Ca10(PO4)6(OH)2; HAP) is an essential component of the human bone inorganic phase. At the nanoscale level, nano-HAP (nHAP) presents marked emergent properties differing substantially from those of the bulk counterpart. Interestingly, these properties depend on nanoparticle characteristics. In this study, we investigated the cytotoxicity of rod-shaped crystalline nHAP (10 −20 nm x 50 −100 nm) in both normal (ARPE-19, BV-2) and tumoral (HepG20 HEp-2, A549 and C6) cells. We found that nHAP was cytotoxic in tumor HEp-2, A549, and C6 cells. Moreover, it induced an expansion of the lysosomal compartment at sublethal concentrations in different cell lines, while lysosomal membrane damage was not detected. In C6 glioma cells, the most sensitive cell line to nHAP, these nanoparticles increased reactive oxygen species (ROS) production and induced DNA damage measured by y-H2AX phosphorylation. Interestingly, our data also show for the first time that nHAP affects both cell unlimited proliferative capacity and cell migration, two of the major pathways involved in cancer progression. The present results showed the cytotoxic and antiproliferative effects of nHAP and suggest its potential as an alternative agent for glioma therapy.
Descripción Física:p.34-42
ISSN:ISSN 1096-0929. Nanohydroxyapatite cytotoxicity in glioma cells