4.5 Article

Breast cancers from black women exhibit higher numbers of immunosuppressive macrophages with proliferative activity and of crown-like structures associated with lower survival compared to non-black Latinas and Caucasians

期刊

BREAST CANCER RESEARCH AND TREATMENT
卷 158, 期 1, 页码 113-126

出版社

SPRINGER
DOI: 10.1007/s10549-016-3847-3

关键词

Breast cancer; Race/ethnicities; Macrophages; Crown-like structures; Inflammation

类别

资金

  1. Braman Family Breast Cancer Institute Development Grant from Sylvester Comprehensive Cancer Center at University of Miami Miller School of Medicine
  2. NCI/NIH [R21CA176055]
  3. Breast Cancer Research Foundation
  4. Play for P.I.N.K.
  5. NIEHS [R01-ES024991]
  6. Women's Cancer Association of UM
  7. Sylvester Comprehensive Cancer Center
  8. [R21CA178675]
  9. [R01CA181115]
  10. [R01CA157012]

向作者/读者索取更多资源

Racial disparities in breast cancer incidence and outcome are a major health care challenge. Patients in the black race group more likely present with an early onset and more aggressive disease. The occurrence of high numbers of macrophages is associated with tumor progression and poor prognosis in solid malignancies. Macrophages are observed in adipose tissues surrounding dead adipocytes in crown-like structures (CLS). Here we investigated whether the numbers of CD163+ tumor-associated macrophages (TAMs) and/or CD163+ CLS are associated with patient survival and whether there are significant differences across blacks, non-black Latinas, and Caucasians. Our findings confirm that race is statistically significantly associated with the numbers of TAMs and CLS in breast cancer, and demonstrate that the highest numbers of CD163+ TAM/CLS are found in black breast cancer patients. Our results reveal that the density of CD206 (M2) macrophages is a significant predictor of progression-free survival univariately and is also significant after adjusting for race and for HER2, respectively. We examined whether the high numbers of TAMs detected in tumors from black women were associated with macrophage proliferation, using the Ki-67 nuclear proliferation marker. Our results reveal that TAMs actively divide when in contact with tumor cells. There is a higher ratio of proliferating macrophages in tumors from black patients. These findings suggest that interventions based on targeting TAMs may not only benefit breast cancer patients in general but also serve as an approach to remedy racial disparity resulting in better prognosis patients from minority racial groups.

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