» Articles » PMID: 27406875

Endocrine Resistance in Hormone-responsive Breast Cancer: Mechanisms and Therapeutic Strategies

Overview
Specialties Endocrinology
Oncology
Date 2016 Jul 14
PMID 27406875
Citations 65
Authors
Affiliations
Soon will be listed here.
Abstract

The majority of breast cancers may be considered hormone responsive due to expression of hormone receptors (HR+). Although endocrine therapy is always considered for advanced HR+ breast cancer, the emergence of resistance is inevitable over time and is present from the start in a proportion of patients. In this review, we explore the mechanisms underlying de novo and acquired resistance to endocrine therapy. We comprehensively review newly approved and emerging therapies that have been developed to counteract specific mechanisms of resistance. We discuss the challenges pertinent to this therapeutic arena including the potential relief of negative regulatory feedback inhibition with compensatory pathway activation and the evolution of molecular changes in HR+ breast cancers during treatment. We discuss strategies to address these challenges in order to develop rational therapy approaches for patients with advanced HR+ breast cancer.

Citing Articles

Expression and clinical significance of CCN5 and the oestrogen receptor in advanced breast cancer.

Zhou G, Qu W, Yang L, Huang A, Gui X BMC Womens Health. 2025; 25(1):89.

PMID: 40016720 PMC: 11866700. DOI: 10.1186/s12905-025-03608-3.


HDAC-driven mechanisms in anticancer resistance: epigenetics and beyond.

Minisini M, Mascaro M, Brancolini C Cancer Drug Resist. 2024; 7:46.

PMID: 39624079 PMC: 11609180. DOI: 10.20517/cdr.2024.103.


PRODH Regulates Tamoxifen Resistance through Ferroptosis in Breast Cancer Cells.

Zhang P, Qian N, Lai H, Chen S, Wu K, Luo X Genes (Basel). 2024; 15(10).

PMID: 39457440 PMC: 11507086. DOI: 10.3390/genes15101316.


Evolving Management of Breast Cancer in the Era of Predictive Biomarkers and Precision Medicine.

Afzal M, Vahdat L J Pers Med. 2024; 14(7).

PMID: 39063972 PMC: 11278458. DOI: 10.3390/jpm14070719.


The Effect of C-Reactive Protein/Lymphocyte Ratio (CLR) on PFS in Metastatic Breast Cancer Patients Treated with CDK4/6 Inhibitors: A Novel Biomarker.

Buyukbayram M, Hannarici Z, Duzkopru Y, Turhan A, Caglar A, Coban Esdur P Breast Cancer (Dove Med Press). 2024; 16:329-339.

PMID: 38974895 PMC: 11227876. DOI: 10.2147/BCTT.S464161.