| Author |
Iyengar, Neil M. Morris, Patrick G. Zhou, Xi Kathy Gucalp, Ayca Giri, Dilip Harbus, Michael D. Falcone, Domenick J. Krasne, Margaret D. Vahdat, Linda T. Subbaramaiah, Kotha Morrow, Monica Hudis, Clifford A. Dannenberg, Andrew J. |
| Description |
Author Affiliation: Iyengar NM ( Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York. Department of Medicine, Weill Cornell Medical College, New York, New York.); Morris PG ( Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.); Zhou XK ( Department of Healthcare Policy and Research, Weill Cornell Medical College, New York, New York.); Gucalp A ( Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York. Department of Medicine, Weill Cornell Medical College, New York, New York.); Giri D ( Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.); Harbus MD ( Department of Medicine, Weill Cornell Medical College, New York, New York.); Falcone DJ ( Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.); Krasne MD ( Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.); Vahdat LT ( Department of Medicine, Weill Cornell Medical College, New York, New York.); Subbaramaiah K ( Department of Medicine, Weill Cornell Medical College, New York, New York.); Morrow M ( Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.); Hudis CA ( Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York. Department of Medicine, Weill Cornell Medical College, New York, New York.); Dannenberg AJ ( Department of Medicine, Weill Cornell Medical College, New York, New York. ajdannen@med.cornell.edu.) |
| Abstract |
Chronic inflammation is recognized as a risk factor for the development of several malignancies. Local white adipose tissue (WAT) inflammation, defined by the presence of dead or dying adipocytes encircled by macrophages that form crown-like structures (CLS), occurs in the breasts (CLS-B) of most overweight and obese women. Previously, we showed that the presence of CLS-B is associated with elevated tissue levels of proinflammatory mediators and aromatase, the rate-limiting enzyme for estrogen biosynthesis. The associated increased levels of aromatase in the breast provide a plausible mechanistic link between WAT inflammation and estrogen-dependent breast cancers. Thus, breast WAT inflammation could be relevant for explaining the high incidence of estrogen-dependent tumors with aging despite diminished circulating estrogen levels after menopause. To explore this possibility, we determined whether menopause in addition to body mass index (BMI) is associated with breast WAT inflammation among 237 prospectively enrolled women. The presence of CLS-B and its severity (CLS-B/cm(2)) as indicators of WAT inflammation correlated with menopausal status (P = 0.008 and P < 0.001) and BMI (P < 0.001 for both). In multivariable analyses adjusted for BMI, the postmenopausal state was independently associated with the presence (P = 0.03) and severity of breast WAT inflammation (P = 0.01). Mean adipocyte size increased in association with CLS-B (P < 0.001). Our findings demonstrate that breast WAT inflammation, which is associated with elevated aromatase levels, is increased in association with the postmenopausal state independent of BMI. Breast WAT inflammation, a process that can potentially be targeted, may help to explain the high incidence of estrogen-dependent tumors in postmenopausal women. |
