Amorphous silica nanoparticles exhibit antitumor activity in triple‐negative breast cancer cells

Author:

Ibarra Agustina1,Ferronato María Julia1,Clemente Valentina1,Barrientos Anabel2,Alonso Eliana Noelia1,Fermento María Eugenia1,Coló Georgina Pamela1,Facchinetti María Marta1ORCID,Curino Alejandro Carlos1,Agotegaray Mariela3ORCID

Affiliation:

1. Laboratorio de Biología del Cáncer, Departamento de Biología Bioquímica y Farmacia (UNS), Instituto de Investigaciones Bioquímicas de Bahía Blanca (INIBIBB) Universidad Nacional del Sur (UNS)—CONICET Bahía Blanca Argentina

2. Servicio de Patología Hospital Interzonal General de Agudos Dr. José Penna Bahía Blanca Argentina

3. Laboratorio de Nanomateriales Híbridos Aplicados, Departamento de Química (UNS), Instituto de Química del Sur Universidad Nacional del Sur (UNS)—CONICET Bahía Blanca Argentina

Abstract

AbstractTriple‐negative breast cancer (TNBC) is an aggressive subtype of breast cancer that is mainly treated with cytotoxic chemotherapy. However, this treatment is not always effective, and an important percentage of patients develop recurrence. Nanomaterials are emerging as alternative treatment options for various diseases, including cancer. This work reports the synthesis, characterization, antitumor activity evaluation, and sub‐acute toxicity studies of two formulations based on amorphous silica nanoparticles (SiNPs). They are functionalized with 3‐aminopropyltriethoxisilane (Si@NH2) and folic acid (FA; Si@FA). The results show that SiNPs reduce the viability and migration of TNBC MDA‐MB‐231 and 4T1 cell lines and Si@FA do not affect the growth of the mammary nonmalignant HC11 cells. In addition, Si@FA induces reactive oxygen species (ROS) generation and displays antiproliferative and subsequently proapoptotic effects in MDA‐MB‐231 cells. Moreover, none of the SiNPs cause signs of sub‐acute toxicity in mice when administered at 30 mg/kg over a month. In conclusion, these nanosystems display intrinsic antitumor activity without causing toxic in vivo effects, being a promising therapeutic alternative for TNBC.

Publisher

Wiley

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