4.5 Article

The Relationship Between White Adipose Tissue Inflammation and Overweight/Obesity in Chinese Female Breast Cancer: A Retrospective Study

Journal

ADVANCES IN THERAPY
Volume 37, Issue 6, Pages 2734-2747

Publisher

SPRINGER
DOI: 10.1007/s12325-020-01368-0

Keywords

Breast neoplasms; Crown-like structures; Inflammation; Obesity; White adipose tissue

Funding

  1. Medical Science and Technology Development Foundation, Nanjing Department of Health [YKK18083]
  2. Medical Science Technology Innovation Platform Project of Nanjing Health Committee [ZDX16006]
  3. Jiangsu Biobank of Clinical Resources [BM2015004]
  4. National Human Genetic Resources Sharing Service Platform [2005DKA21300]

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Introduction This study aims to investigate the relationship between breast white adipose tissue (WAT) inflammation and being overweight or obese, menopausal status, and metabolic syndrome-related indicators in breast cancer patients as well as the association between adipocyte size and the severity of WAT inflammation and body mass index (BMI). Methods The crown-like structures (CLS-B) formed by macrophages surrounding dying or dead adipocytes can be used to identify breast WAT inflammation. In this study, breast WAT and fasting blood from 136 Chinese women with breast cancer were collected for analysis. Cluster of differentiation 68 (CD68) immunohistochemical staining was performed to identify CLS-B, and the adipocyte size was measured by hematoxylin and eosin staining. Results The results showed that breast WAT inflammation usually occurs in overweight/obese breast cancer patients, and the severity of inflammation is positively correlated with adipocyte hypertrophy. We did not observe a direct association between WAT inflammation and menopausal status. In addition, the presence of WAT inflammation is associated with abnormalities in circulating factors associated with metabolic syndrome such as higher serum lipid, glucose, and C-reactive protein levels. Conclusion Overweight/obese breast cancer patients may be more prone to breast WAT inflammation and may be associated with abnormalities in circulatory markers associated with metabolic syndrome.

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