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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Folic acid-doxorubicin polymeric nanocapsules: A promising formulation for the treatment of triple-negative breast cancer

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Autor(es):
Ce, Rodrigo [1] ; Couto, Gabriela Klein [2] ; Pacheco, Barbara Zoche [3] ; Dallemole, Danieli Rosane [1] ; Paschoal, Julia Dame [2] ; Pacheco, Bruna Silveira [2] ; Guterres, Silvia Staniscuaski [1] ; Seixas, Fabiana [2] ; Collares, Tiago [2] ; Pohlmann, Adriana Raffin [1, 3]
Número total de Autores: 10
Afiliação do(s) autor(es):
[1] Univ Fed Rio Grande do Sul, Fac Farm, Programa Posgrad Ciencias Farmaceut, Av Ipiranga 2752, BR-90610000 Porto Alegre, RS - Brazil
[2] Univ Fed Pelotas, Lab Biotecnol Canc, Grp Pesquisa Oncol Celular & Mol, Programa Posgrad Biotecnol, Biotecnol Ctr Desenvol, Pelotas, RS - Brazil
[3] Univ Fed Rio Grande do Sul, Inst Quim, Dept Quim Organ, Av Bento Gonsalves 9500, BR-91501970 Porto Alegre, RS - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: European Journal of Pharmaceutical Sciences; v. 165, OCT 1 2021.
Citações Web of Science: 0
Resumo

Breast cancer is the most common cancers among women and is one of the main causes of morbidity and mortality in this population. In this study, we aimed to conjugate doxorubicin (DOX), a drug widely used in cancer chemotherapy, and folic acid (FA), a ligand targeted for cancer therapy, to lipid-core nanocapsules (LNC), and evaluate the efficacy of the nanoformulation against triple-negative breast cancer (TNBC) MDA-MB-231 cells that overexpress folate receptors (FRs). We performed cell viability assays, quantitative real-time PCR (qRTPCR), cell migration assay, and clonogenic assay, as well as measured the levels of nitric oxide (NO) generated and cellular uptake. The results showed that the nanoformulation reduced cell viability. The results of qRT-PCR analysis revealed that the nanoformulation induced apoptosis of MDA-MB-231 cells. The mRNA expression levels of Cat and MnSod were increased when the nanoformulation was compared to the doxorubicin solution. Furthermore, the nanoformulation significantly decreased the migration of breast cancer cells in vitro and inhibited colony formation. Additionally, the expression of iNOS in MDA-MB-231 cells was higher when the nanoformulation was used compared to the doxorubicin solution. Cellular uptake was observed after incubating the MDA-MB-231 cells with the fluorescent-labeled nanoformulation. In conclusion, we developed a promising nanoformulation for the treatment of TNBC. Further studies are necessary to demonstrate the in vivo efficacy of this formulation. (AU)

Processo FAPESP: 14/50928-2 - INCT 2014: Nanotecnologia Farmacêutica: uma abordagem transdisciplinar
Beneficiário:Maria Vitória Lopes Badra Bentley
Modalidade de apoio: Auxílio à Pesquisa - Temático