Leek R D, Lewis C E, Whitehouse R, Greenall M, Clarke J, Harris A L
Imperial Cancer Research Fund Molecular Oncology Laboratory, University of Oxford Institute of Molecular Medicine, England.
Cancer Res. 1996 Oct 15;56(20):4625-9.
Angiogenesis is a key process in tumor growth and metastasis and is a major independent prognostic factor in breast cancer. A range of cytokines stimulate the tumor neovasculature, and tumor-associated macrophages have been shown recently to produce several important angiogenic factors. We have quantified macrophage infiltration using Chalkley count morphometry in a series of invasive breast carcinomas to investigate the relationship between tumor-associated macrophage infiltration and tumor angiogenesis, and prognosis. There was a significant positive correlation between high vascular grade and increased macrophage index (P = 0.03), and a strong relationship was observed between increased macrophage counts and reduced relapse-free survival (P = 0.006) and reduced overall survival (P = 0.004) as an independent prognostic variable. These data indicate a role for macrophages in angiogenesis and prognosis in breast cancer and that this cell type may represent an important target for immunoinhibitory therapy in breast cancer.
血管生成是肿瘤生长和转移的关键过程,也是乳腺癌主要的独立预后因素。一系列细胞因子刺激肿瘤新生血管生成,最近研究表明肿瘤相关巨噬细胞可产生多种重要的血管生成因子。我们采用Chalkley计数形态学方法对一系列浸润性乳腺癌中的巨噬细胞浸润情况进行定量分析,以研究肿瘤相关巨噬细胞浸润与肿瘤血管生成及预后之间的关系。高血管分级与巨噬细胞指数增加之间存在显著正相关(P = 0.03),并且作为独立预后变量,巨噬细胞计数增加与无复发生存期缩短(P = 0.006)和总生存期缩短(P = 0.004)之间存在密切关系。这些数据表明巨噬细胞在乳腺癌血管生成和预后中发挥作用,并且这种细胞类型可能是乳腺癌免疫抑制治疗的重要靶点。