Analysis of the cellular viability and migratory capacity of triple-negative breast cancer cells stimulated with doxorubicin used during neoadjuvant chemotherapy (#1479)
Read ArticleDate of Conference
July 15-17, 2026
Published In
"Engineering without Borders: Artificial Intelligence, Knowledge, Innovation, and Alliances for a Future from the Americas"
Location of Conference
Santiago (Chile)
Authors
Vallejos Paredes, María Fernanda
Buitron Mercado, Melissa Francesca
Carpio-Carpio, Jose Miguel
Ita Balta, Yuma Aracely
Riera Perez, Angeline Caprice
Villanueva-Salas, José Antonio
Choquenaira-Quispe, Celia
Abstract
Breast cancer remains a major public health problem, especially the triple-negative molecular subtype, due to its limited response to chemotherapy. Therefore, the objective of this study was to evaluate the cellular viability and migratory capacity of triple-negative breast cancer cells treated with doxorubicin, a drug used in neoadjuvant chemotherapy. For this purpose, the MDA-MB-231 cell line was used, cultured in DMEM medium supplemented with 10% fetal bovine serum and 1% antibiotic. Response to treatment was evaluated using MTT, clonogenic, and wound healing assays. The results showed an IC₅₀ value of 0.3 µM for doxorubicin in the MDA-MB-231 cell line. It was also observed that, despite treatment, the cells retained partial migratory capacity. Taken together, these findings indicate that doxorubicin reduces cell viability but does not completely inhibit the migration of MDA-MB-231 cells, which could contribute to doxorubicin favoring the survival of this triple-negative molecular phenotype.