Montironi R, Santinelli A, Magi Galluzzi C, Giannulis I
Institute of Morbid Anatomy and Histopathology, School of Medicine, University of Ancona, Nuovo Ospedale Regionale, Torrette di Ancona, Italy.
In Vivo. 1993 Jul-Aug;7(4):343-6.
The aim of this study was to emphasise the importance of the measurement sites in tumours from the biological point of view. In particular, two distinct aspects regarding locations were investigated for Proliferating Cell Nuclear Antigen (PCNA) expression in the cribriform adenocarcinoma of the prostate as an example. The first aspect was the identification of the most suitable part of the tumour nodule to be analysed, that is, periphery or marginal zone vs central. The second aspect consisted of the precise location of the objects in relation to the histologic pattern and its components, such as the different cell layers in the cribriform pattern. The results obtained showed that the proportion of PCNA-immunostained nuclei in the marginal zone of the tumour decreased from the basal position, or adjacent to the stroma, towards the lumen: 14.40% (standard error, SE, 0.61%) in the basal position, 11.84% (SE 1.30%) in the intermediate and 9.26% (SE 0.66%) in the lumenal position. In the central zone of the tumour the trend of value changes was similar to that obtained in the marginal zone. However, the proportions were lower and the differences statistically significant. In conclusion, the degree of PCNA expression is related to both locations. Thus, adequate information on the biology of the lesions can only be obtained when the precise site of the objects to be evaluated is identified. Otherwise, misleading results about the lesions being measured can be derived.
本研究的目的是从生物学角度强调肿瘤测量部位的重要性。特别是,以前列腺筛状腺癌中增殖细胞核抗原(PCNA)的表达为例,研究了与位置相关的两个不同方面。第一个方面是确定肿瘤结节中最适合分析的部分,即周边或边缘区与中央区。第二个方面包括根据组织学模式及其组成部分,如筛状模式中的不同细胞层,精确确定物体的位置。所得结果表明,肿瘤边缘区PCNA免疫染色细胞核的比例从基底位置(即靠近基质处)向管腔方向逐渐降低:基底位置为14.40%(标准误差,SE,0.61%),中间位置为11.84%(SE 1.30%),管腔位置为9.26%(SE 0.66%)。在肿瘤中央区,数值变化趋势与边缘区相似。然而,比例较低且差异具有统计学意义。总之,PCNA表达程度与两个位置均相关。因此,只有在确定待评估物体的精确位置时,才能获得有关病变生物学的充分信息。否则,可能会得出有关所测量病变的误导性结果。