| Literature DB >> 33922898 |
Sílvia Rocha-Rodrigues1,2,3, Andreia Matos3,4, José Afonso5, Miguel Mendes-Ferreira3, Eduardo Abade6, Eduardo Teixeira1,7,8, Bruno Silva1,2, Eugenia Murawska-Ciałowicz9, Maria José Oliveira3, Ricardo Ribeiro3,10,11.
Abstract
Increased visceral adiposity may influence the development of prostate cancer (PCa) aggressive tumors and cancer mortality. White adipose tissue (WAT), usually referred to as periprostatic adipose tissue (PPAT), surrounds the prostatic gland and has emerged as a potential mediator of the tumor microenvironment. Exercise training (ET) induces several adaptations in both skeletal muscle and WAT. Some of these effects are mediated by ET-induced synthesis and secretion of several proteins, known as myo- and adipokines. Together, myokines and adipokines may act in an endocrine-like manner to favor communication between skeletal muscle and WAT, as they may work together to improve whole-body metabolic health. This crosstalk may constitute a potential mechanism by which ET exerts its beneficial role in the prevention and treatment of PCa-related disorders; however, this has not yet been explored. Therefore, we reviewed the current evidence on the effects of skeletal muscle-WAT-tumor crosstalk in PCa, and the potential mediators of this process to provide a better understanding of underlying ET-related mechanisms in cancer.Entities:
Keywords: cancer; periprostatic fat; physical activity; skeletal muscle; tumor microenvironment; visceral adiposity
Year: 2021 PMID: 33922898 DOI: 10.3390/ijms22094469
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923