Obesity and endocrine therapy resistance in breast cancer: Mechanistic insights and perspectives.
Ines BaroneAmanda CarusoLuca GelsominoCinzia GiordanoDaniela BonofiglioStefania CatalanoSebastiano AndòPublished in: Obesity reviews : an official journal of the International Association for the Study of Obesity (2021)
The incidence of obesity, a recognized risk factor for various metabolic and chronic diseases, including numerous types of cancers, has risen dramatically over the recent decades worldwide. To date, convincing research in this area has painted a complex picture about the adverse impact of high body adiposity on breast cancer onset and progression. However, an emerging but overlooked issue of clinical significance is the limited efficacy of the conventional endocrine therapies with selective estrogen receptor modulators (SERMs) or degraders (SERDs) and aromatase inhibitors (AIs) in patients affected by breast cancer and obesity. The mechanisms behind the interplay between obesity and endocrine therapy resistance are likely to be multifactorial. Therefore, what have we actually learned during these years and which are the main challenges in the field? In this review, we will critically discuss the epidemiological evidence linking obesity to endocrine therapeutic responses and we will outline the molecular players involved in this harmful connection. Given the escalating global epidemic of obesity, advances in understanding this critical node will offer new precision medicine-based therapeutic interventions and more appropriate dosing schedule for treating patients affected by obesity and with breast tumors resistant to endocrine therapies.
Keyphrases
- insulin resistance
- weight loss
- metabolic syndrome
- high fat diet induced
- weight gain
- type diabetes
- end stage renal disease
- ejection fraction
- estrogen receptor
- newly diagnosed
- adipose tissue
- chronic kidney disease
- skeletal muscle
- emergency department
- risk factors
- prognostic factors
- mesenchymal stem cells
- peritoneal dialysis
- lymph node
- single molecule
- patient reported
- replacement therapy
- breast cancer risk