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Differential Expression of NOTCH-1 and Its Molecular Targets in Response to Metronomic Followed by Conventional Therapy in a Patient with Advanced Triple-Negative Breast Cancer

Authors :
Ilari, A
Cogliati, V
Sherif, N
Grassilli, E
Ramazzotti, D
Cordani, N
Cazzaniga, G
Di Bella, C
Lavitrano, M
Cazzaniga, M
Cerrito, M
Ilari, Alice
Cogliati, Viola
Sherif, Noorhan
Grassilli, Emanuela
Ramazzotti, Daniele
Cordani, Nicoletta
Cazzaniga, Giorgio
Di Bella, Camillo
Lavitrano, Marialuisa
Cazzaniga, Marina Elena
Cerrito, Maria Grazia
Ilari, A
Cogliati, V
Sherif, N
Grassilli, E
Ramazzotti, D
Cordani, N
Cazzaniga, G
Di Bella, C
Lavitrano, M
Cazzaniga, M
Cerrito, M
Ilari, Alice
Cogliati, Viola
Sherif, Noorhan
Grassilli, Emanuela
Ramazzotti, Daniele
Cordani, Nicoletta
Cazzaniga, Giorgio
Di Bella, Camillo
Lavitrano, Marialuisa
Cazzaniga, Marina Elena
Cerrito, Maria Grazia
Publication Year :
2024

Abstract

A group of 27 patients diagnosed with metastatic triple-negative breast cancer (mTNBC) was randomly distributed into two groups and underwent different lines of metronomic treatment (mCHT). The former group (N 14) received first-line mCHT and showed a higher overall survival rate than the second group (N 13), which underwent second-line mCHT. Analysis of one patient still alive from the first group, diagnosed with mTNBC in 2019, showed a complete metabolic response (CMR) after a composite approach implicating first-line mCHT followed by second-line epirubicin and third-line nab-paclitaxel, and was chosen for subsequent molecular characterization. We found altered expression in the cancer stemness-associated gene NOTCH-1 and its corresponding protein. Additionally, we found changes in the expression of oncogenes, such as MYC and AKT, along with their respective proteins. Overall, our data suggest that a first-line treatment with mCHT followed by MTD might be effective by negatively regulating stemness traits usually associated with the emergence of drug resistance.

Details

Database :
OAIster
Notes :
ELETTRONICO, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1427430984
Document Type :
Electronic Resource