| Literature DB >> 33316954 |
Emma Zattarin1, Rita Leporati1, Francesca Ligorio1, Riccardo Lobefaro1, Andrea Vingiani1, Giancarlo Pruneri1,2, Claudio Vernieri1,3.
Abstract
Hormone receptor-positive breast cancer (HR+ BC) accounts for approximately 75% of new BC diagnoses. Despite the undisputable progresses obtained in the treatment of HR+ BC in recent years, primary or acquired resistance to endocrine therapies still represents a clinically relevant issue, and is largely responsible for disease recurrence after curative surgery, as well as for disease progression in the metastatic setting. Among the mechanisms causing primary or acquired resistance to endocrine therapies is the loss of estrogen/progesterone receptor expression, which could make BC cells independent of estrogen stimulation and, consequently, resistant to estrogen deprivation or the pharmacological inhibition of estrogen receptors. This review aims at discussing the molecular mechanisms and the clinical implications of HR loss as a result of the therapies used in the neoadjuvant setting or for the treatment of advanced disease in HR+ BC patients.Entities:
Keywords: (neo)adjuvant therapy; breast cancer; clonal selection; conversion; endocrine therapies; hormone receptors; intratumor heterogeneity; re-characterization; tumor recurrences
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Year: 2020 PMID: 33316954 PMCID: PMC7764472 DOI: 10.3390/cells9122644
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600