Werness B A, Freedman A N, Piver M S, Romero-Gutierrez M, Petrow E
Division of Pathology, Roswell Park Cancer Institute, Buffalo, New York 14263, USA.
Gynecol Oncol. 1999 Dec;75(3):413-8. doi: 10.1006/gyno.1999.5601.
Theprognostic value of p53 expression in epithelial ovarian cancer remains unresolved. We hypothesized that prognosis may relate more to expression of p21(waf1/cip1), the major downstream effector of p53, which can also be induced through p53-independent mechanisms. We therefore studied the relationship of p53 and p21(waf1/cip1) expression in epithelial ovarian cancers to clinicopathological variables and prognosis.
Fixed, embedded tumors from 85 patients with untreated, primary epithelial ovarian cancer were immunostained with antibodies to p53 and p21(waf1/cip1). Expression was correlated with clinicopathological features and prognosis. Survival curves were calculated by the Kaplan-Meier method and compared using the log-rank test for p53, p21(waf1/cip1), and all combinations of expression of the two markers.
Sixty-two percent of tumors expressed p53, and 42% expressed p21(waf1/cip1). There was no correlation between p53 and p21(waf1/cip1) expression. Advanced stage, grade, age >/=50, and p53 expression were associated with worse disease-free survival. Patients whose tumors were p53(+)/waf1(-), however, had a particularly strong association with poorer disease-free survival when compared with other combinations of p53 and p21(waf1/cip1) expression (P = 0.003). Neither p53, nor p21(waf1/cip1), nor combinations of expression were independently related to survival when histology, age, stage, and differentiation were considered.
p53 expression in the absence of p21(waf1/cip1) expression is a better marker of poor prognosis than either p53 or p21(waf1/cip1) expression status alone in univariate analysis. Absence of independent prognostic significance may be related to the paucity of early stage cases in the current study.
p53表达在上皮性卵巢癌中的预后价值仍未明确。我们推测预后可能与p21(waf1/cip1)的表达关系更为密切,p21(waf1/cip1)是p53的主要下游效应分子,其也可通过p53非依赖机制诱导产生。因此,我们研究了上皮性卵巢癌中p53和p21(waf1/cip1)的表达与临床病理变量及预后的关系。
对85例未经治疗的原发性上皮性卵巢癌患者的固定、包埋肿瘤组织用p53和p21(waf1/cip1)抗体进行免疫染色。将表达情况与临床病理特征及预后进行关联分析。采用Kaplan-Meier法计算生存曲线,并使用对数秩检验对p53、p21(waf1/cip1)以及两种标志物表达的所有组合进行比较。
62%的肿瘤表达p53,42%表达p21(waf1/cip1)。p53与p21(waf1/cip1)的表达之间无相关性。晚期、高级别、年龄≥50岁以及p53表达与无病生存期较差相关。然而,与p53和p21(waf1/cip1)表达的其他组合相比,肿瘤为p53(+)/waf1(-)的患者与较差的无病生存期具有特别强的相关性(P = 0.003)。当考虑组织学、年龄、分期和分化情况时,p53、p21(waf1/cip1)及其表达组合均与生存无独立相关性。
在单变量分析中,p53表达而无p21(waf1/cip1)表达比单独的p53或p21(waf1/cip1)表达状态更能提示预后不良。缺乏独立的预后意义可能与本研究中早期病例较少有关。