| First Author | Drew BG | Year | 2015 |
| Journal | J Biol Chem | Volume | 290 |
| Issue | 9 | Pages | 5566-81 |
| PubMed ID | 25468909 | Mgi Jnum | J:329480 |
| Mgi Id | MGI:6835168 | Doi | 10.1074/jbc.M114.606459 |
| Citation | Drew BG, et al. (2015) Estrogen receptor (ER)alpha-regulated lipocalin 2 expression in adipose tissue links obesity with breast cancer progression. J Biol Chem 290(9):5566-81 |
| abstractText | Obesity is associated with increased breast cancer (BrCA) incidence. Considering that inactivation of estrogen receptor (ER)alpha promotes obesity and metabolic dysfunction in women and female mice, understanding the mechanisms and tissue-specific sites of ERalpha action to combat metabolic-related disease, including BrCA, is of clinical importance. To study the role of ERalpha in adipose tissue we generated fat-specific ERalpha knock-out (FERKO) mice. Herein we show that ERalpha deletion increased adipocyte size, fat pad weight, and tissue expression and circulating levels of the secreted glycoprotein, lipocalin 2 (Lcn2), an adipokine previously associated with BrCA development. Chromatin immunoprecipitation and luciferase reporter studies showed that ERalpha binds the Lcn2 promoter to repress its expression. Because adipocytes constitute an important cell type of the breast microenvironment, we examined the impact of adipocyte ERalpha deletion on cancer cell behavior. Conditioned medium from ERalpha-null adipocytes and medium containing pure Lcn2 increased proliferation and migration of a subset of BrCA cells in culture. The proliferative and promigratory effects of ERalpha-deficient adipocyte-conditioned medium on BrCA cells was reversed by Lcn2 deletion. BrCA cell responsiveness to exogenous Lcn2 was heightened in cell types where endogenous Lcn2 expression was minimal, but components of the Lcn2 signaling pathway were enriched, i.e. SLC22A17 and 3-hydroxybutyrate dehydrogenase (BDH2). In breast tumor biopsies from women diagnosed with BrCA we found that BDH2 expression was positively associated with adiposity and circulating Lcn2 levels. Collectively these data suggest that reduction of ERalpha expression in adipose tissue promotes adiposity and is linked with the progression and severity of BrCA via increased adipocyte-specific Lcn2 production and enhanced tumor cell Lcn2 sensitivity. |
