Toll-like receptor 4–induced inflammatory responses contribute to the tumor-associated macrophages formation and infiltration in patients with diffuse large B-cell lymphoma

Abstract To evaluate the expression of tumor-associated macrophages (TAMs) and Toll-like receptor 4 (TLR4) in diffuse large B-cell lymphoma (DLBCL) and their correlation with patient clinical characteristics, we detected using immunohistochemistry in 81 specimens of patients with DLBCL. The correlat...

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Veröffentlicht in:Annals of diagnostic pathology 2015-08, Vol.19 (4), p.232-238
Hauptverfasser: Wang, Xiaofang, MD, Li, Xiangli, MS, Zhang, Xiaoying, MS, Zang, Li, MS, Yang, Hongliang, MS, Zhao, Weipeng, MD, Zhao, Haifeng, MD, Li, Qian, MS, Xia, Bing, MS, Yu, Yong, MD, Wang, Yafei, MD, Zhao, Zhigang, MD, Zhang, Yizhuo, PhD
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Sprache:eng
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Zusammenfassung:Abstract To evaluate the expression of tumor-associated macrophages (TAMs) and Toll-like receptor 4 (TLR4) in diffuse large B-cell lymphoma (DLBCL) and their correlation with patient clinical characteristics, we detected using immunohistochemistry in 81 specimens of patients with DLBCL. The correlation between protein expression levels and clinical parameters, as well as the association between CD68 and TLR4 were analyzed. The number of CD68 TAMs was closely related to β2 -microglobulin ( P = .028 and P < .05), whereas there was no significant correlation between the number of CD68 TAMs and other clinical factors. Toll-like receptor 4 was related to tumor size and peripheral blood lymphocyte to monocyte ratio. The Spearman correlation coefficient indicated a significant positive correlation between CD68 TAMs and TLR4 expression ( r = 0.240; P = .038, P = .05). These results, on one hand, indicated that TLR4-induced inflammatory responses may affect TAM infiltration and accumulation, and that TAMs and TLR4 may interact to play important roles in DLBCL microenvironment regulating the tumor growth, but, on the other hand demonstrated that both of TAMs and TLR4 had not only one side on DLBCL growth.
ISSN:1092-9134
1532-8198
DOI:10.1016/j.anndiagpath.2015.04.008