4.6 Article

Blood biomarkers reflect the effects of obesity and inflammation on the human breast transcriptome

Journal

CARCINOGENESIS
Volume 42, Issue 10, Pages 1281-1292

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/carcin/bgab066

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Funding

  1. National Institutes of Health/National Cancer Institute [U54CA210184-01]
  2. Breast Cancer Research Foundation
  3. ICONIIC seed grant
  4. Botwinick-Wolfensohn Foundation
  5. Memorial Sloan Kettering Cancer Center Support Grant/Core Grant [P30 CA008748]

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Obesity and breast white adipose tissue inflammation are associated with increased risk of post-menopausal breast cancer. Through analyzing molecular changes in breast tissues and blood biomarkers, this study helps to explain the link between obesity and breast cancer, highlighting the potential utility of blood biomarkers in determining risk and prognosis.
Obesity is a risk factor for the development of post-menopausal breast cancer. Breast white adipose tissue (WAT) inflammation, which is commonly found in women with excess body fat, is also associated with increased breast cancer risk. Both local and systemic effects are probably important for explaining the link between excess body fat, adipose inflammation and breast cancer. The first goal of this cross-sectional study of 196 women was to carry out transcriptome profiling to define the molecular changes that occur in the breast related to excess body fat and WAT inflammation. A second objective was to determine if commonly measured blood biomarkers of risk and prognosis reflect molecular changes in the breast. Breast WAT inflammation was assessed by immunohistochemistry. Bulk RNA-sequencing was carried out to assess gene expression in non-tumorous breast. Obesity and WAT inflammation were associated with a large number of differentially expressed genes and changes in multiple pathways linked to the development and progression of breast cancer. Altered pathways included inflammatory response, complement, KRAS signaling, tumor necrosis factor alpha signaling via NFkB, interleukin (IL)6-JAK-STAT3 signaling, epithelial mesenchymal transition, angiogenesis, interferon gamma response and transforming growth factor (TGF)-beta signaling. Increased expression of several drug targets such as aromatase, TGF-beta 1, IDO-1 and PD-1 were observed. Levels of various blood biomarkers including high sensitivity C-reactive protein, IL6, leptin, adiponectin, triglycerides, high-density lipoprotein cholesterol and insulin were altered and correlated with molecular changes in the breast. Collectively, this study helps to explain both the link between obesity and breast cancer and the utility of blood biomarkers for determining risk and prognosis.

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