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
Alice Ilari,
Viola Cogliati,
Noorhan Sherif,
Emanuela Grassilli,
Daniele Ramazzotti,
Nicoletta Cordani,
Giorgio Cazzaniga,
Camillo Di Bella,
Marialuisa Lavitrano,
Marina Elena Cazzaniga,
Maria Grazia Cerrito
Affiliations
Alice Ilari
School of Medicine and Surgery, Milano-Bicocca University, 20900 Monza, Italy
Viola Cogliati
Phase 1 Research Centre, Fondazione IRCCS San Gerardo dei Tintori, Via Pergolesi 33, 20900 Monza, Italy
Noorhan Sherif
School of Medicine and Surgery, Milano-Bicocca University, 20900 Monza, Italy
Emanuela Grassilli
School of Medicine and Surgery, Milano-Bicocca University, 20900 Monza, Italy
Daniele Ramazzotti
School of Medicine and Surgery, Milano-Bicocca University, 20900 Monza, Italy
Nicoletta Cordani
School of Medicine and Surgery, Milano-Bicocca University, 20900 Monza, Italy
Giorgio Cazzaniga
Department of Pathology, Fondazione IRCCS San Gerardo dei Tintori, Via Pergolesi 33, 20900 Monza, Italy
Camillo Di Bella
Department of Pathology, Fondazione IRCCS San Gerardo dei Tintori, Via Pergolesi 33, 20900 Monza, Italy
Marialuisa Lavitrano
School of Medicine and Surgery, Milano-Bicocca University, 20900 Monza, Italy
Marina Elena Cazzaniga
School of Medicine and Surgery, Milano-Bicocca University, 20900 Monza, Italy
Maria Grazia Cerrito
School of Medicine and Surgery, Milano-Bicocca University, 20900 Monza, Italy
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.