Stephenson T J, Royds J A, Bleehen S S, Silcocks P B, Rees R C
Department of Pathology, University of Sheffield Medical School, UK.
Dermatology. 1993;187(2):95-9. doi: 10.1159/000247214.
An inverse correlation has been demonstrated between nm23 gene expression and metastasis. The gene is located on chromosome 17q (q1.1-q2.1), a region distinct from tumour suppressor gene p53. We have previously reported expression of mutant products of p53 gene to be significantly associated with worsening degrees of differentiation in squamous cell carcinoma. nm23 gene product, which shows complete identity to human erythrocyte nucleoside diphosphate kinase, was used to raise an affinity-purified polyclonal antibody Ab-11 which is applicable to formalin-fixed and paraffin-embedded tissues. Keratoacanthomas and squamous cell carcinomas of the epidermis form a fascinating human tumour model in which to test the hypothesis that the nm23 gene confers 'anti-metastatic' properties, since the former never metastasise while the latter have this potential. Two observers rated immunohistochemistry for the nm23 gene product as the proportion of tumour positive from grades 1-4 (corresponding to 25, 50, 75 and 100% of tumour cells stained). Nineteen typical keratoacanthomas, 20 well, 21 moderately and 8 poorly differentiated epidermal squamous cell carcinomas were studied. The Jonckheere-Terpstra test statistic of association between staining grade and lesion type was 762.5, p = 0.189 (2 tails), p = 0.0945 (1 tail). There was no statistically significant trend in tumour staining from keratoacanthoma through decreasing grades of differentiation of squamous cell carcinoma. nm23 product expression does not appear to correlate with differentiation, itself an indicator of metastatic potential, in this system of human squamous cell neoplasms.(ABSTRACT TRUNCATED AT 250 WORDS)
已证实nm23基因表达与转移之间存在负相关。该基因位于17号染色体q(q1.1 - q2.1)上,这是一个与肿瘤抑制基因p53不同的区域。我们之前曾报道,p53基因的突变产物表达与鳞状细胞癌的分化程度恶化显著相关。nm23基因产物与人红细胞核苷二磷酸激酶完全相同,用于制备适用于福尔马林固定和石蜡包埋组织的亲和纯化多克隆抗体Ab - 11。表皮的角化棘皮瘤和鳞状细胞癌构成了一个引人入胜的人类肿瘤模型,可用于检验nm23基因赋予“抗转移”特性这一假说,因为前者从不转移而后者有转移的可能。两名观察者将nm23基因产物的免疫组织化学结果评定为肿瘤阳性比例,分为1 - 4级(分别对应25%、50%、75%和100%的肿瘤细胞染色)。研究了19例典型角化棘皮瘤、20例高分化、21例中分化和8例低分化的表皮鳞状细胞癌。染色分级与病变类型之间关联的Jonckheere - Terpstra检验统计量为762.5,p = 0.189(双侧),p = 0.0945(单侧)。从角化棘皮瘤到鳞状细胞癌分化程度降低,肿瘤染色无统计学显著趋势。在这个人类鳞状细胞肿瘤系统中,nm23产物表达似乎与分化无关,而分化本身是转移潜能的一个指标。(摘要截选至250字)