| Literature DB >> 33525605 |
Vanessa Castelli1, Mariano Catanesi1, Margherita Alfonsetti1, Chiara Laezza2, Francesca Lombardi1, Benedetta Cinque1, Maria Grazia Cifone1, Rodolfo Ippoliti1, Elisabetta Benedetti1, Annamaria Cimini1,3, Michele d'Angelo1.
Abstract
Breast cancer is the most frequent cancer and the second leading cause of death among women. Triple-negative breast cancer is the most aggressive subtype of breast cancer and is characterized by the absence of hormone receptors and human epithelial growth factor receptor 2. Cancer stem cells (CSCs) represent a small population of tumor cells showing a crucial role in tumor progression, metastasis, recurrence, and drug resistance. The presence of CSCs can explain the failure of conventional therapies to completely eradicate cancer. Thus, to overcome this limit, targeting CSCs may constitute a promising approach for breast cancer treatment, especially in the triple-negative form. To this purpose, we isolated and characterized breast cancer stem cells from a triple-negative breast cancer cell line, MDA-MB-231. The obtained mammospheres were then treated with the specific PPARα antagonist GW6471, after which, glucose, lipid metabolism, and invasiveness were analyzed. Notably, GW6471 reduced cancer stem cell viability, proliferation, and spheroid formation, leading to apoptosis and metabolic impairment. Overall, our findings suggest that GW6471 may be used as a potent adjuvant for gold standard therapies for triple-negative breast cancer, opening the possibility for preclinical and clinical trials for this class of compounds.Entities:
Keywords: CSCs; MDA-MB-231; mammospheres; metabolism; spheroids; triple-negative breast cancer
Year: 2021 PMID: 33525605 PMCID: PMC7912302 DOI: 10.3390/biomedicines9020127
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059