Nakopoulou L, Constantinides C, Papandropoulos J, Theodoropoulos G, Tzonou A, Giannopoulos A, Zervas A, Dimopoulos C
Department of Pathology and Urology, Athens University Medical School, Greece.
Urology. 1995 Sep;46(3):334-40. doi: 10.1016/S0090-4295(99)80216-7.
p53 tumor suppressor gene is considered to play a significant role in carcinogenesis. Mutations in the p53 are the most frequent genetic abnormalities encountered in human malignancies. Our aim was to investigate the expression of p53 oncoprotein in superficial and invasive transitional cell bladder cancer (TCC) as well as its correlation with established prognostic factors, such as histologic grade, tumor stage, DNA content, and survival.
Forty-five patients with superficial TCC (Ta-T1) and 42 with invasive TCC (T2-T4) were included in our study. Material from transurethral biopsy was examined using an immunohistochemical method and the monoclonal antibody Pab 1801.
p53 tumor suppressor protein was overexpressed in 48.3% of TCC cases and more frequently in invasive than superficial TCCs (P = 0.03) and undetectable in the tumor adjacent to normal tissue. p53 positivity was related to the degree of differentiation and with the stage of the disease of invasive TCCs (P = 0.03 and P = 0.004, respectively), whereas no statistical significance was documented for superficial TCCs. Moreover, p53 overexpression demonstrated a statistical significance with DNA ploidy in superficial Ta-T1 tumors (P = 0.04) and was suggestive in invasive T2-T4 tumors (P = 0.08). There was no correlation of recurrence related to p53-positive superficial tumors (P = 0.29). Patients with p53-positive invasive TCCs showed statistically significant worse survival (P = 0.007), but in multivariate analysis, p53 positivity is not independently related to poor overall survival (P = 0.30). When we combined ploidy and p53 status, we realized that the subset of patients with aneuploidy and p53 positivity had the worst prognosis (P = 0.008).
The results suggest the involvement of p53 protein as a late event in bladder carcinogenesis. p53 does not seem to be a prognostic marker for recurrences of superficial tumors and is not independently related to survival. The aneuploidy of tumors correlates with the p53 positivity in bladder cancer. The combined expression of aneuploidy and p53 positivity in invasive tumors has strong association with the survival of patients.
p53肿瘤抑制基因被认为在致癌过程中起重要作用。p53基因的突变是人类恶性肿瘤中最常见的基因异常。我们的目的是研究p53癌蛋白在浅表性和浸润性膀胱移行细胞癌(TCC)中的表达及其与既定预后因素的相关性,如组织学分级、肿瘤分期、DNA含量和生存率。
本研究纳入了45例浅表性TCC(Ta-T1)患者和42例浸润性TCC(T2-T4)患者。经尿道活检材料采用免疫组织化学方法和单克隆抗体Pab 1801进行检测。
p53肿瘤抑制蛋白在48.3%的TCC病例中过度表达,在浸润性TCC中比浅表性TCC更常见(P = 0.03),在正常组织相邻的肿瘤中未检测到。p53阳性与浸润性TCC的分化程度和疾病分期相关(分别为P = 0.03和P = 0.004),而浅表性TCC未显示统计学意义。此外,p53过度表达在浅表Ta-T1肿瘤中与DNA倍体具有统计学意义(P = 0.04),在浸润性T2-T4肿瘤中具有提示意义(P = 0.08)。p53阳性的浅表肿瘤与复发无相关性(P = 0.29)。p53阳性的浸润性TCC患者的生存率在统计学上显著较差(P = 0.007),但在多变量分析中,p53阳性与总体生存率差无独立相关性(P = 0.30)。当我们将倍体和p53状态结合起来时,我们发现非整倍体和p53阳性的患者亚组预后最差(P = 0.008)。
结果表明p53蛋白参与膀胱致癌过程中的晚期事件。p53似乎不是浅表肿瘤复发的预后标志物,且与生存率无独立相关性。肿瘤的非整倍体与膀胱癌中的p53阳性相关。浸润性肿瘤中非整倍体和p53阳性的联合表达与患者生存率密切相关。