Author(s): Martins, Sara A. ; Costa, Rui R. ; Brito, Alexandra ; Reis, R. L. ; Alves, N. M. ; Pashkuleva, I. ; Soares da Costa, Diana
Date: 2024
Persistent ID: https://hdl.handle.net/1822/93817
Origin: RepositóriUM - Universidade do Minho
Subject(s): Breast cancer; Calcium overload; Cell spheroids; Core/shell nanoparticles; Doxorubicin; Hyaluronic acid
Targeted breast cancer therapies hold the potential to improve the efficiency of drug delivery to the pathology site without impacting the viability and function of healthy cells. Herein, we developed multifunctional nanocarriers that target simultaneously several downstream signaling processes in triple negative breast cancer cells. The system comprises pH sensitive CaCO3 nanoparticles (NPs) as carriers of the anticancer drug doxorubicin (DOX). The NPs were coated in a layer-by-layer (LbL) fashion using poly-L-lysine and hyaluronic acid to target receptors overexpressed in breast cancer (e.g. CD44, RHAMM). Spheroids of the triple-negative Hs578T cell line were used as a 3D model to assess the therapeutic potential of this system. Our results showed that the NPs act via a synergistic mechanism that combines Ca2+ overload causing cell calcification and DNA damage by DOX. The LbL coating was crucial for the protection of the healthy cells, i.e. it provides NPs with targeting capacity. The overall data suggests that the LbL-coated NPs loaded with DOX hold great potential for the treatment of breast cancer.
