Systemic Correlates of White Adipose Tissue Inflammation in Early-Stage Breast Cancer

Clin Cancer Res. 2016 May 1;22(9):2283-9. doi: 10.1158/1078-0432.CCR-15-2239. Epub 2015 Dec 28.

Abstract

Purpose: Obesity, insulin resistance, and elevated levels of circulating proinflammatory mediators are associated with poorer prognosis in early-stage breast cancer. To investigate whether white adipose tissue (WAT) inflammation represents a potential unifying mechanism, we examined the relationship between breast WAT inflammation and the metabolic syndrome and its prognostic importance.

Experimental design: WAT inflammation was defined by the presence of dead/dying adipocytes surrounded by macrophages forming crown-like structures (CLS) of the breast. Two independent groups were examined in cross-sectional (cohort 1) and retrospective (cohort 2) studies. Cohort 1 included 100 women undergoing mastectomy for breast cancer risk reduction (n = 10) or treatment (n = 90). Metabolic syndrome-associated circulating factors were compared by CLS-B status. The association between CLS of the breast and the metabolic syndrome was validated in cohort 2, which included 127 women who developed metastatic breast cancer. Distant recurrence-free survival (dRFS) was compared by CLS-B status.

Results: In cohorts 1 and 2, breast WAT inflammation was detected in 52 of 100 (52%) and 52 of 127 (41%) patients, respectively. Patients with breast WAT inflammation had elevated insulin, glucose, leptin, triglycerides, C-reactive protein, and IL6 and lower high-density lipoprotein cholesterol and adiponectin (P < 0.05) in cohort 1. In cohort 2, breast WAT inflammation was associated with hyperlipidemia, hypertension, and diabetes (P < 0.05). Compared with patients without breast WAT inflammation, the adjusted HR for dRFS was 1.83 (95% CI, 1.07-3.13) for patients with inflammation.

Conclusions: WAT inflammation, a clinically occult process, helps to explain the relationship between metabolic syndrome and worse breast cancer prognosis. Clin Cancer Res; 22(9); 2283-9. ©2015 AACR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Adipocytes / pathology
  • Adipose Tissue, White / metabolism
  • Adipose Tissue, White / pathology*
  • Adult
  • Aged
  • Breast / metabolism
  • Breast / pathology
  • Breast Neoplasms / etiology
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology*
  • C-Reactive Protein / metabolism
  • Cross-Sectional Studies
  • Female
  • Glucose / metabolism
  • Humans
  • Inflammation / etiology
  • Inflammation / metabolism
  • Inflammation / pathology*
  • Insulin / metabolism
  • Interleukin-6 / metabolism
  • Leptin / metabolism
  • Macrophages / metabolism
  • Macrophages / pathology
  • Metabolic Syndrome / metabolism
  • Metabolic Syndrome / pathology
  • Middle Aged
  • Obesity / complications
  • Obesity / metabolism
  • Obesity / pathology
  • Retrospective Studies
  • Triglycerides / metabolism

Substances

  • Insulin
  • Interleukin-6
  • Leptin
  • Triglycerides
  • C-Reactive Protein
  • Glucose