Cargando…

Combination of plasma HA and circulating M2-like monocytes may serve as a diagnostic marker for breast cancer

Background: Breast cancer (BC)-derived hyaluronan (HA) can induce the formation of M2-like tumor-associated macrophages (TAMs) in tumor context. However, little is known about the correlation between circulating M2-like monocytes and plasma HA in BC patients. This study focused on evaluating the rel...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Boke, Cao, Manlin, He, Yiqing, Liu, Yiwen, Zhang, Guoliang, Yang, Cuixia, Du, Yan, Xu, Jing, Hu, Jiajie, Gao, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687167/
https://www.ncbi.nlm.nih.gov/pubmed/29151937
http://dx.doi.org/10.7150/jca.20227
Descripción
Sumario:Background: Breast cancer (BC)-derived hyaluronan (HA) can induce the formation of M2-like tumor-associated macrophages (TAMs) in tumor context. However, little is known about the correlation between circulating M2-like monocytes and plasma HA in BC patients. This study focused on evaluating the relationship between circulating M2-like monocytes and plasma HA, and further appraised the diagnostic value of them in BC. Methods: The expression of M2-like TAMs and HA was determined in pathological tissues by immunohistochemistry. Flow cytometry was used to detect the levels of circulating CD14(+)CD204(+) M2-like monocytes in 81 BC patients, 45 patients with breast benign diseases, and 46 healthy subjects. The levels of HA, CEA, and CA15-3 were measured in plasma samples using chemiluminescence method. Results: M2-like TAMs and HA expressions were elevated in BC tissues compared with benign tissues. In correspondence, the frequency of circulating CD14(+)CD204(+) M2-like monocytes and the plasma HA levels were significantly higher in patients with BC than those in control groups. Importantly, there was a positive correlation between circulating M2-like monocytes and the plasma HA (Spearman r = 0.404, p < 0.001). Area under receiver operating characteristic curve (ROC) for the combination of circulating M2-like monocytes and HA was 0.899 (95% CI: 0.853-0.946), which was higher than the panel of CEA and CA15-3. Conclusions: The frequency of circulating CD14(+)CD204(+) M2-like monocytes was positively correlated to plasma HA levels. The combination of circulating CD14(+)CD204(+) M2-like monocytes and plasma HA could provide considerable diagnostic value in BC.