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[核仁组成区嗜银蛋白分析在恶性肿瘤中的重要性]

[Importance of AgNOR analysis in malignant tumors].

作者信息

Martin H

机构信息

Institut für Pathologie, Paritätisches Krankenhaus Berlin-Lichtenberg (Bereich Oskar-Ziethen-Krankenhaus), Deutschland.

出版信息

Zentralbl Pathol. 1994 Mar;140(1):15-22.

PMID:8204559
Abstract

For the assessment of proliferative activity of malignant tumors several methods can be used. The method having been used at first has been the determination of mitotic index, playing an important role as a part of various grading systems until now. Besides of DNA cytometry, flow cytometry, determination of bromodeoxyuridine labeling index (BrdUr-LI) and immunohistochemical analysis of proliferation-associated antigens (e.g. Ki-67, PCNA), for several years AgNOR analysis has been used as a new technique, giving reproducible, exact results of proliferative activity of malignant tumors. Valuable information about proliferative activity of cells can be gained already by counting the AgNOR number per nucleus. Moreover the use of digital image analysis provides information about size and distribution of AgNORs. Evidently these data are more important than AgNOR number. In the hands of experienced pathologists and under standardized conditions AgNOR staining and AgNOR quantification are a valuable completion of established methods.

摘要

对于恶性肿瘤增殖活性的评估,可以使用多种方法。最初使用的方法是有丝分裂指数的测定,直到现在它在各种分级系统中都起着重要作用。除了DNA细胞计数法、流式细胞术、溴脱氧尿苷标记指数(BrdUr-LI)的测定以及增殖相关抗原(如Ki-67、PCNA)的免疫组织化学分析外,多年来,核仁组成区嗜银蛋白(AgNOR)分析一直作为一种新技术使用,可给出恶性肿瘤增殖活性的可重复、准确结果。通过计算每个细胞核中的AgNOR数量,已经可以获得有关细胞增殖活性的有价值信息。此外,数字图像分析的使用提供了有关AgNOR大小和分布的信息。显然,这些数据比AgNOR数量更重要。在经验丰富的病理学家手中并在标准化条件下,AgNOR染色和AgNOR定量是对现有方法的有价值补充。

相似文献

1
[Importance of AgNOR analysis in malignant tumors].[核仁组成区嗜银蛋白分析在恶性肿瘤中的重要性]
Zentralbl Pathol. 1994 Mar;140(1):15-22.
2
[Nucleolus organizer regions in pathomorphologic tumor diagnosis].[核仁组织区在肿瘤病理形态学诊断中的应用]
Veroff Pathol. 1992;139:1-144.
3
[AgNOR analysis of astrocytoma in childhood].[儿童星形细胞瘤的银染核仁组成区分析]
Zentralbl Neurochir. 1996;57(1):5-11.
4
[Significance of the AgNOR in tumor pathology].
Pathologica. 2002 Feb;94(1):2-9.
5
AgNOR quantification with special reference to staining patterns.
Zentralbl Pathol. 1994 Mar;140(1):23-30.
6
In vivo bromodeoxyuridine labelling index, AgNOR protein expression and DNA content in human tumours.人体肿瘤中的体内溴脱氧尿苷标记指数、核仁组成区嗜银蛋白表达及DNA含量
Eur J Histochem. 1996;40(1):17-26.
7
Standardized demonstration of silver-stained nucleolar organizer regions-associated proteins in archival oral squamous cell carcinomas and adjacent non-neoplastic mucosa.存档口腔鳞状细胞癌及相邻非肿瘤性黏膜中银染核仁组织区相关蛋白的标准化展示
Mod Pathol. 1997 Feb;10(2):98-104.
8
An improved system for quantifying AgNOR and PCNA in canine tumors.
Anticancer Res. 2000 Sep-Oct;20(5A):3273-80.
9
AgNOR proteins as a parameter of the rapidity of cell proliferation.
Zentralbl Pathol. 1994 Mar;140(1):7-10.
10
Sequential quantification of AgNOR area and number during silver staining by means of an image analysing system.通过图像分析系统对银染色过程中AgNOR面积和数量进行连续定量分析。
Zentralbl Pathol. 1994 Mar;140(1):37-40.

引用本文的文献

1
Improvement of the method for demonstration of nucleolar organizer regions (NORs) in formalin fixed and paraffin embedded tissue using microwave pretreatment.利用微波预处理改进在福尔马林固定石蜡包埋组织中显示核仁组织区(NORs)的方法。
Pflugers Arch. 1996;431(6 Suppl 2):R269-70. doi: 10.1007/BF02346372.