Back to Search Start Over

Moderate swimming suppressed the growth and metastasis of the transplanted liver cancer in mice model: with reference to nervous system.

Authors :
Zhang QB
Zhang BH
Zhang KZ
Meng XT
Jia QA
Zhang QB
Bu Y
Zhu XD
Ma DN
Ye BG
Zhang N
Ren ZG
Sun HC
Tang ZY
Source :
Oncogene [Oncogene] 2016 Aug 04; Vol. 35 (31), pp. 4122-31. Date of Electronic Publication: 2015 Dec 21.
Publication Year :
2016

Abstract

Physical activity has been shown to suppress tumor initiation and progression. The neurotransmitter dopamine (DA) is closely related to movement and exhibits antitumor properties. However, whether the suppressive effects of physical activity on tumors was mediated by the nervous system via increased DA level remains unknowns. Here we show that regular moderate swimming (8 min/day, 9 weeks) raised DA levels in the prefrontal cortex, serum and tumor tissue, suppressed growth, reduced lung metastasis of transplanted liver cancer, and prolonged survival in a C57BL/6 mouse model, while overload swimming (16 and 32 min/day, 9 weeks) had the opposite effect. In nude mice that were orthotopically implanted with human liver cancer cell lines, DA treatment significantly suppressed growth and lung metastasis by acting on the D2 receptor (DR2). Furthermore, DR2 blockade attenuated the suppressive effect of moderate swimming on liver cancer. Both moderate swimming and DA treatment suppressed the transforming growth factor-beta (TGF-β1)-induced epithelial-mesenchymal transition of transplanted liver cancer cells. At the molecular level, DR2 signaling inhibited extracellular signal-regulated kinase phosphorylation and expression of TGF-β1 in vitro. Together, these findings demonstrated a novel mechanism by which the moderate exercise suppressed liver cancer through boosting DR2 activity, while overload exercise had the opposite effect, highlighting the possible importance of the dopaminergic system in tumor growth and metastasis of liver cancer.

Details

Language :
English
ISSN :
1476-5594
Volume :
35
Issue :
31
Database :
MEDLINE
Journal :
Oncogene
Publication Type :
Academic Journal
Accession number :
26686088
Full Text :
https://doi.org/10.1038/onc.2015.484