Rüschoff J
Institut für Pathologie, Universität Marburg.
Veroff Pathol. 1992;139:1-144.
Morphology and biological behaviour of tumours are closely related to each other and are the main objects of diagnostic tumour pathology. Anaplasia, for example, a well-known cytomorphological criterion of malignancy, is however only an indirect sign of impaired cellular growth control mechanisms. Nowadays, it is a goal of cancer research to investigate these regulatory processes in order to elucidate new diagnostic criteria of malignancy. Silver staining of nucleolar organizer regions (AgNORs) basically meets this new concept. NORs (rDNA) encode for ribosomal RNA and are thus of central importance for the protein synthesis of a cell. Silver stains NOR associated proteins and indicates activated rDNA. Therefore, AgNOR staining covers the proliferative potential of a given cell or a tumour respectively. A prerequisite of reliable application of the AgNOR method to diagnostic tumour pathology is standardization of the technique, which should be based upon scientific results obtained by basic research. Accordingly, in interphasic cells AgNORs are primarily substructures of nucleoli corresponding to the fibrillar centers at the ultrastructural level. This has been shown to be an important criterion to determine the quality of the silver staining reaction. Most artifacts result from inadequate tissue preservation (fixation), unspecific argyrophilic structures and the staining procedure itself. They should either be excluded or--when ever possible--controlled by a proper staining technique, i.e. adjustment to the stainability of every individual specimen. In this respect, digital image analysis proved to be a useful tool. The mean size of AgNORs in small lymphocytes of the same tissue sample is an equivalent of the argyrophilia of a given histological and cytological specimen (internal staining standard). By use of such a standardized staining technique a high diagnostic accuracy is achieved. The proliferative potential of a cell or a tumour can be determined by number, size, staining intensity and distribution of the silver stained dots. In histological tissue sections the quotient of the mean number of AgNORs/cell and the mean area of one AgNOR dot/cell has been shown to be a very sensitive diagnostic parameter. In cytological specimens determination of the total silver stained area per cell is superior to counting of AgNORs simply by eye. Normal and malignant tissue can reliably be discriminated by these morphometric values. In addition, the malignancy potential of the different preneoplastic lesions, e.g. of the urinary bladder, can precisely be described. Flat urothelial lesions with moderate cytological atypia (D2) exhibit AgNOR values in the range of well differentiated papillary carcinomas.(ABSTRACT TRUNCATED AT 400 WORDS)
肿瘤的形态学和生物学行为密切相关,是肿瘤诊断病理学的主要研究对象。例如,间变作为一种众所周知的恶性细胞形态学标准,仅仅是细胞生长控制机制受损的间接标志。如今,癌症研究的一个目标是研究这些调控过程,以阐明新的恶性诊断标准。核仁组织区银染色(AgNORs)基本符合这一新概念。核仁组织区(rDNA)编码核糖体RNA,因此对细胞的蛋白质合成至关重要。银染与核仁组织区相关的蛋白质,并显示活化的rDNA。因此,AgNOR染色分别反映了给定细胞或肿瘤的增殖潜能。将AgNOR方法可靠地应用于肿瘤诊断病理学的一个前提是技术的标准化,这应以基础研究获得的科学结果为依据。因此,在间期细胞中,AgNORs主要是核仁的亚结构,在超微结构水平上对应于纤维中心。这已被证明是确定银染色反应质量的一个重要标准。大多数伪像源于组织保存(固定)不当、非特异性嗜银结构和染色过程本身。应通过适当的染色技术将它们排除或尽可能加以控制,即根据每个标本的可染性进行调整。在这方面,数字图像分析被证明是一个有用的工具。同一组织样本中小淋巴细胞中AgNORs的平均大小相当于给定组织学和细胞学标本的嗜银性(内部染色标准)。通过使用这种标准化染色技术可实现较高的诊断准确性。细胞或肿瘤的增殖潜能可通过银染点的数量、大小、染色强度和分布来确定。在组织学切片中,平均每个细胞的AgNORs数量与平均每个AgNOR点的面积之比已被证明是一个非常敏感的诊断参数。在细胞学标本中,测定每个细胞的总银染面积优于单纯肉眼计数AgNORs。通过这些形态学测量值可以可靠地区分正常组织和恶性组织。此外,还可以精确描述不同癌前病变(如膀胱)的恶性潜能。具有中度细胞异型性(D2)的扁平尿路上皮病变的AgNOR值处于高分化乳头状癌范围内。