Related Experiment Video
Updated: Jan 23, 2026

An Ex vivo Model to Study Hormone Action in the Human Breast
Published on: January 8, 2015
Endocrine Resistance in Hormone Receptor Positive Breast Cancer-From Mechanism to Therapy
Aradhana Rani1, Justin Stebbing2, Georgios Giamas3
1School of Life Sciences, University of Westminster, London, United Kingdom.
Abstract:
The importance and role of the estrogen receptor (ER) pathway has been well-documented in both breast cancer (BC) development and progression. The treatment of choice in women with metastatic breast cancer (MBC) is classically divided into a variety of endocrine therapies, 3 of the most common being: selective estrogen receptor modulators (SERM), aromatase inhibitors (AI) and selective estrogen receptor down-regulators (SERD). In a proportion of patients, resistance develops to endocrine therapy due to a sophisticated and at times redundant interference, at the molecular level between the ER and growth factor. The progression to endocrine resistance is considered to be a gradual, step-wise process. Several mechanisms have been proposed but thus far none of them can be defined as the complete explanation behind the phenomenon of endocrine resistance. Although multiple cellular, molecular and immune mechanisms have been and are being extensively studied, their individual roles are often poorly understood. In this review, we summarize current progress in our understanding of ER biology and the molecular mechanisms that predispose and determine endocrine resistance in breast cancer patients.
Related Concept Videos
Endocrine Signaling
Intracellular Hormone Receptors
Types of Hormones
Hormonal Regulation
Hormonal Regulation
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...

