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]
日期:2001-01-01
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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