Significant correlation of monocyte chemoattractant protein-1 expression with neovascularization and progression of breast carcinoma

医学 川地68 病理 血管生成 新生血管 免疫组织化学 趋化因子 单核细胞 乳腺癌 肿瘤进展 分级(工程) 乳腺癌 癌症研究 炎症 癌症 免疫学 生物 内科学 生态学
作者
Hisashi Saji,Morio Koike,Takao Yamori,Shigehira Saji,Motoharu Seiki,Kouji Matsushima,Masakazu Toi
出处
期刊:Cancer [Wiley]
卷期号:92 (5): 1085-1091 被引量:286
标识
DOI:10.1002/1097-0142(20010901)92:5<1085::aid-cncr1424>3.0.co;2-k
摘要

BACKGROUND: Macrophages often infiltrate into solid tumor tissues. Tumor-associated macrophages (TAMs) are known to play a crucial role in tumor progression. Monocyte chemoattractant protein-1 (MCP-1) is one of the major chemokines capable of inducing chemotactic migration of monocytes. METHODS: With the objective of investigating the clinical significance of MCP-1, the authors analyzed the expression of MCP-1 and of some other molecules by immunohistochemistry in 230 samples of primary breast carcinoma tissue. MCP-1 staining was performed using an anti-MCP-1 monoclonal antibody, and it was assessed by grading the percentage of stained cells. RESULTS: It was found that 117 breast tumor specimens (51%) had intensive staining in tumor cells. The expression of MCP-1 in tumor cells had a significant correlation with the expression of thymidine phosphorylase and membrane type 1-matrix metalloproteinase. In addition, MCP-1 expression tended to be associated with the accumulation of TAMs, which were counted by CD68 staining, and with microvessel density. MCP-1 expression in TAMs was correlated significantly with the histologic vessel invasion of tumor cells. CONCLUSIONS: The results of this study suggest that MCP-1 may play key roles in macrophage recruitment, in the expression of angiogenic factors, and in the activation of matrix metalloproteinases in patients with breast carcinoma.

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