Mineta H, Borg A, Dictor M, Wahlberg P, Akervall J, Wennerberg J
Department of Otorhinolaryngology/H&N Surgery, University Hospital, Lund, Sweden.
Br J Cancer. 1998 Oct;78(8):1084-90. doi: 10.1038/bjc.1998.632.
Survival in squamous cell carcinoma of the head and neck (HNSCC) was compared with overexpression and mutation of the p53 gene. Archival tissue from 77 tumours was analysed for protein expression using immunohistochemistry (IHC) with the monoclonal antibody Do-7, and for the presence of mutation in exons 5-8 using single-stranded conformation polymorphism (SSCP), followed by DNA sequencing in SSCP-positive cases. p53 expression was scored as high (>70% nuclei stained) in 25 (32%) tumours, as intermediate (10-70% nuclei stained) in 19 (25%) tumours and as low (<10% nuclei stained) in 33 (43%) tumours. Twelve (18%) tumours exhibited gene mutation (ten missense and two nonsense mutations) and an additional five tumours contained changes that could not result in amino acid substitution or protein truncation. There was no correlation between gene expression and mutation, mutations being equally frequent in tumours with either high (4/25), intermediate (4/19) or low protein expression (4/33). Fifty-eight patients were eligible for survival analysis. There was a strong correlation between p53 mutation and cause-specific survival; median survival among mutated cases was 12.5 months compared with >160 months among non-mutated patients (P < 0.005). There was no correlation between p53 overexpression and survival. The results suggest that p53 mutation status is an important prognostic factor in HNSCC, and that IHC analysis of protein overexpression is an inadequate measure of gene mutation in these tumours.
对头颈部鳞状细胞癌(HNSCC)患者的生存情况与p53基因的过表达及突变情况进行了比较。采用单克隆抗体Do-7通过免疫组织化学(IHC)分析了77例肿瘤存档组织的蛋白表达情况,并采用单链构象多态性(SSCP)分析了外显子5 - 8的突变情况,对SSCP阳性病例进行DNA测序。p53表达情况评分如下:25例(32%)肿瘤为高表达(>70%细胞核染色),19例(25%)肿瘤为中等表达(10% - 70%细胞核染色),33例(43%)肿瘤为低表达(<10%细胞核染色)。12例(18%)肿瘤出现基因突变(10例错义突变和2例无义突变),另有5例肿瘤存在不会导致氨基酸替代或蛋白质截短的变化。基因表达与突变之间无相关性,在高表达(4/25)、中等表达(4/19)或低蛋白表达(4/33)的肿瘤中,突变频率相同。58例患者符合生存分析条件。p53突变与特定病因生存率之间存在强相关性;突变病例的中位生存期为12.5个月,而未突变患者的中位生存期>160个月(P < 0.005)。p53过表达与生存率之间无相关性。结果表明,p53突变状态是HNSCC的一个重要预后因素,并且对这些肿瘤进行蛋白过表达的IHC分析不足以衡量基因突变情况。