Askensten U
Department of Tumour Pathology, Karolinska Institute and Hospital, Stockholm, Sweden.
Arch Geschwulstforsch. 1988;58(6):431-9.
Cytochemical assessments of the nuclear DNA contents in carcinomas of the breast can be used for both prognostic and diagnostic purposes. Two main techniques are currently being used, viz. flow cytometry (FCM) and microspectrophotometry (MSP). An account of their advantages and disadvantages is given. In addition, an old, rather crude, cytophotometric technique can be used for histopathological sections of paraffin-embedded specimens. The principal sampling procedures are fine-needle aspiration biopsy and the so-called imprint technique, where the specimens are made from the cut surface of the freshly excised operation specimen. Paraffin-embedded histopathological material can also be used, applying a newly developed MSP procedure, where isolated nuclei from deparaffinized/disintegrated specimens are analyzed. Most important is that intact cell nuclei, representative for the whole tumour nodule, can be obtained. The simultaneous use of FCM and MSP is also of utmost importance for the reliability in the interpretation of the results. Then, a kind of "DNA malignancy grading" is obtained that in several investigations has proven itself to be an excellent prognosticating tool that can be used for making an adequate choice of therapy for the individual patient. The diagnostic value of the results of the cytochemically assessed nuclear DNA distribution patterns is not so high as the prognostic one. Tumours with a diploid type of nuclear DNA content can be found both among benign and malignant neoplasms. However, a neoplasm with an aneuploid DNA distribution pattern can almost certainly be considered highly malignant.
乳腺癌细胞核DNA含量的细胞化学评估可用于预后和诊断目的。目前主要使用两种技术,即流式细胞术(FCM)和显微分光光度法(MSP)。文中阐述了它们的优缺点。此外,一种古老且较为粗糙的细胞光度技术可用于石蜡包埋标本的组织病理学切片。主要的采样程序是细针穿刺活检和所谓的印片技术,标本取自新鲜切除手术标本的切面。也可使用石蜡包埋的组织病理学材料,应用一种新开发的MSP程序,分析从脱蜡/解离标本中分离出的细胞核。最重要的是能够获得代表整个肿瘤结节的完整细胞核。同时使用FCM和MSP对于结果解释的可靠性也至关重要。这样就能得出一种“DNA恶性分级”,在多项研究中已证明其是一种出色的预后工具,可用于为个体患者做出合适的治疗选择。细胞化学评估的细胞核DNA分布模式结果的诊断价值不如预后价值高。在良性和恶性肿瘤中都可发现核DNA含量为二倍体类型的肿瘤。然而,具有非整倍体DNA分布模式的肿瘤几乎肯定可被视为高度恶性。