[Human mammary carcinoma. A model for the relationship between tumor proliferation, tumor-associate macrophages, and prognostic factors].

H Müller
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Abstract

As compared with the lymphatic system, the mononuclear phagocyte system (MPS) represents the older defense system in the course of evolution. Organisms with defective or with no lymphocytic function are able to live for a certain time while metazoa cannot develop and exist without cells capable of phagocytosis. It is known that up to 80% of the mass of malignant experimental tumors may consist of macrophages. The biological relevance of these tumor-associated macrophages (TAM), however, is contested to date. Besides well-known tasks in specific and non-specific defense, the cells of the MPS possess nutritive functions. The different functions of TAM have been essentially examined in animal experiments in vivo and in vitro up to now. These studies have shown, e.g., that TAM of different phenotypes to some extent are assigned to different functions and that each tumor or tumor cell line has a specific TAM pattern. The available number of monoclonal antibodies (MAB) able to recognize different groups of human macrophages has only increased in the recent past. This also provided evidence of the phenotypic heterogeneity of macrophages in the human system. On the other hand, there is little knowledge to date of the possible biological cause of the presence of numerous macrophages also in the stroma of malignant tumors in man and on the functional relevance of particular macrophage phenotypes. In the present studies, the phenotypic pattern of tumor-associated cells was examined by immunohistochemistry in the model of human mammary carcinoma, using 18 monoclonal antibodies (Ki-M1-8, Leu-M1-3, Leu-M5, EBM11, CD1, anti-transferrin receptor [TFR], anti-MHC I, anti-MHC II or anti HLA-DR) and one polyclonal antibody (anti protein-S100). The first part of the study contains a semiquantitative evaluation of 216 cases of mammary carcinoma. The analytical results are correlated with established prognostic factors available in the case of malignant tumors in general and in that of mammary carcinomas in particular (age, menopausal status of patients, axillary lymph node and estrogen/progesterone receptor status, size of tumor, tumor type according to WHO, degree of malignancy according to histopathological and nuclear grading). As tumor parameters of absolute biological relevance, proliferating activity (Ki67) and MHC phenotype of tumor cells and amount or types of tumor-associated lymphocytes (TAL) are examined in order to analyze their correlation with prognostic factors and their importance in the tumor-macrophage system.(ABSTRACT TRUNCATED AT 400 WORDS)

人类乳腺癌。肿瘤增殖、肿瘤相关巨噬细胞和预后因素之间关系的模型[d]。
与淋巴系统相比,单核吞噬细胞系统(MPS)是进化过程中较古老的防御系统。有淋巴细胞功能缺陷或没有淋巴细胞功能的生物体能够存活一段时间,而后生动物没有能够吞噬的细胞就不能发育和存在。据了解,高达80%的恶性实验性肿瘤肿块可能由巨噬细胞组成。然而,这些肿瘤相关巨噬细胞(TAM)的生物学相关性至今仍有争议。除了众所周知的特异性和非特异性防御任务外,MPS细胞还具有营养功能。迄今为止,TAM的不同功能在体内和体外的动物实验中已经得到了基本的研究。例如,这些研究表明,不同表型的TAM在一定程度上具有不同的功能,每种肿瘤或肿瘤细胞系具有特定的TAM模式。能够识别不同人群的人巨噬细胞的单克隆抗体(MAB)的数量在最近才有所增加。这也为巨噬细胞在人体系统中的表型异质性提供了证据。另一方面,迄今为止,对于人类恶性肿瘤间质中大量巨噬细胞存在的可能生物学原因以及特定巨噬细胞表型的功能相关性知之甚少。本研究利用18种单克隆抗体(Ki-M1-8、Leu-M1-3、Leu-M5、EBM11、CD1、抗转铁蛋白受体[TFR]、抗mhc I、抗mhc II或抗HLA-DR)和1种多克隆抗体(抗蛋白- s100),采用免疫组化方法检测人乳腺癌模型中肿瘤相关细胞的表型。研究的第一部分包括对216例乳腺癌的半定量评估。分析结果与一般恶性肿瘤,特别是乳腺癌的既定预后因素相关(患者的年龄、绝经状态、腋窝淋巴结和雌激素/孕激素受体状态、肿瘤大小、世界卫生组织规定的肿瘤类型、组织病理学和核分级规定的恶性程度)。作为具有绝对生物学相关性的肿瘤参数,我们检测肿瘤细胞的增殖活性(Ki67)和MHC表型以及肿瘤相关淋巴细胞(TAL)的数量或类型,以分析它们与预后因素的相关性及其在肿瘤-巨噬细胞系统中的重要性。(摘要删节为400字)
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