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Environmental and Genetic Activation of a Brain-Adipocyte BDNF/Leptin Axis Causes Cancer Remission and Inhibition
Author(s) -
Lei Cao,
Xianglan Liu,
EnJu D. Lin,
Chuansong Wang,
Eugene Choi,
Véronique Riban,
Benjamin C. Lin,
Matthew J. During
Publication year - 2010
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2010.05.029
Subject(s) - leptin , biology , endocrinology , downregulation and upregulation , neurotrophic factors , medicine , gene knockdown , adipocyte , cancer , brain derived neurotrophic factor , adipokine , neurotrophin , cancer research , adipose tissue , cell culture , obesity , gene , receptor , genetics
Cancer is influenced by its microenvironment, yet broader, environmental effects also play a role but remain poorly defined. We report here that mice living in an enriched housing environment show reduced tumor growth and increased remission. We found this effect in melanoma and colon cancer models, and that it was not caused by physical activity alone. Serum from animals held in an enriched environment (EE) inhibited cancer proliferation in vitro and was markedly lower in leptin. Hypothalamic brain-derived neurotrophic factor (BDNF) was selectively upregulated by EE, and its genetic overexpression reduced tumor burden, whereas BDNF knockdown blocked the effect of EE. Mechanistically, we show that hypothalamic BDNF downregulated leptin production in adipocytes via sympathoneural beta-adrenergic signaling. These results suggest that genetic or environmental activation of this BDNF/leptin axis may have therapeutic significance for cancer.

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