Zhu Q, White F H, Tipoe G L
Department of Anatomy, University of Hong Kong, Hong Kong.
Oral Oncol. 1997 Jan;33(1):29-35. doi: 10.1016/s0964-1955(96)00038-3.
Immunoreactivity of proliferating cell nuclear antigen (PCNA) was assessed in formalin-fixed, paraffin-embedded sections from human normal parotid gland (N; n = 12), chronic sialadenitis (CS; n = 8), Warthin's tumour (W; n = 10), benign pleomorphic adenoma (BPA; n = 11), mucoepidermoid carcinoma (MEC; n = 14), carcinoma in pleomorphic adenoma (CPA; n = 10) and adenoid cystic carcinoma (ACC; n = 12) of the parotid gland, using the monoclonal antibody PC 10. The morphometric parameters measured comprised PCNA labelling induces (PI = the numerical percentage of PCNA positive nuclei) and volume densities of PCNA positive nuclei(VV, PEP = the relative volume of positive nuclei per unit volume of reference epithelium). All parameters were expressed in relation to total positive, as well as to strongly- and weakly-positive nuclei. In general, the values of PCNA parameters increased progressively in benign lesions in comparison with the N group, and in malignant neoplasms in comparison with non-neoplastic groups and benign lesions. The strongly-positive parameters showed more statistically significant differences than weakly-positive ones, suggesting that weakly-stained nuclei may include some non-cycling cells and, therefore, that weakly-positive parameters may not be reliable proliferation markers. Values for all parameters in CPA were significantly higher than those in BPA, suggesting that these parameters may be used as diagnostic discriminators. Spearman rank correlation analysis showed a highly positive correlation between the morphometric parameters and the severity of the lesions. Furthermore, the mean values of PISP were significantly higher in patients who died of the malignant tumours than in those patients who survived. Our results indicate that PCNA indices might be useful markers for discriminating between benign (BPA) and malignant tumours of the parotid gland and that the parameter PISP may have prognostic applications.
使用单克隆抗体PC 10,对来自人类正常腮腺(N;n = 12)、慢性涎腺炎(CS;n = 8)、沃辛瘤(W;n = 10)、良性多形性腺瘤(BPA;n = 11)、黏液表皮样癌(MEC;n = 14)、多形性腺瘤癌变(CPA;n = 10)和腮腺腺样囊性癌(ACC;n = 12)的福尔马林固定、石蜡包埋切片中的增殖细胞核抗原(PCNA)免疫反应性进行评估。所测量的形态计量学参数包括PCNA标记指数(PI = PCNA阳性细胞核的数字百分比)和PCNA阳性细胞核的体积密度(VV,PEP = 每单位参考上皮体积中阳性细胞核的相对体积)。所有参数均相对于总阳性以及强阳性和弱阳性细胞核表示。一般来说,与N组相比,良性病变中PCNA参数的值逐渐增加,与非肿瘤组和良性病变相比,恶性肿瘤中PCNA参数的值逐渐增加。强阳性参数比弱阳性参数显示出更多的统计学显著差异,这表明弱阳性细胞核可能包括一些非循环细胞,因此弱阳性参数可能不是可靠的增殖标志物。CPA中所有参数的值均显著高于BPA中的值,这表明这些参数可作为诊断鉴别指标。Spearman等级相关分析显示形态计量学参数与病变严重程度之间存在高度正相关。此外,死于恶性肿瘤的患者的PISP平均值显著高于存活患者。我们的结果表明,PCNA指数可能是区分腮腺良性(BPA)和恶性肿瘤的有用标志物,并且参数PISP可能具有预后应用价值。