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细胞核p53的积累与膀胱癌的肿瘤进展

Accumulation of nuclear p53 and tumor progression in bladder cancer.

作者信息

Esrig D, Elmajian D, Groshen S, Freeman J A, Stein J P, Chen S C, Nichols P W, Skinner D G, Jones P A, Cote R J

机构信息

Department of Urology, University of Southern California School of Medicine, Los Angeles 90033.

出版信息

N Engl J Med. 1994 Nov 10;331(19):1259-64. doi: 10.1056/NEJM199411103311903.

Abstract

BACKGROUND

We have previously demonstrated a strong association between nuclear accumulation of p53 protein, as determined by immunohistochemical analysis, and mutations in the p53 gene. The purpose of this study was to determine the relation between nuclear accumulation of p53 and tumor progression in transitional-cell carcinoma of the bladder.

METHODS

Histologic specimens of transitional-cell carcinoma of the bladder (stages Pa, noninvasive disease, to P4, disease with direct extension into adjacent organs or structures) from 243 patients who were treated by radical cystectomy were examined for the immunohistochemical detection of p53 protein. Nuclear p53 reactivity was then analyzed in relation to time to recurrence and overall survival.

RESULTS

The detection of nuclear p53 was significantly associated with an increased risk of recurrence of bladder cancer (P < 0.001) and with decreased overall survival (P < 0.001). In patients with cancer confined to the bladder, the rates of recurrence for stage P1, P2, and P3a tumors that had no detectable nuclear p53 reactivity at five years were 7, 12, and 11 percent, respectively, as compared with 62, 56, and 80 percent, respectively, for tumors that had p53 immunoreactivity. Similar results were obtained when the presence or absence of p53 in the nuclei of the tumor cells was studied in relation to overall survival. In a multivariable analysis stratified according to grade, pathological stage, and lymph-node status, nuclear p53 status was an independent predictor (and in cancer confined to the bladder, the only independent predictor) of recurrence and overall survival (P < 0.001).

CONCLUSIONS

In patients with transitional-cell carcinoma confined to the bladder, an accumulation of p53 in the tumor-cell nuclei detected by immunohistochemical methods predicts a significantly increased risk of recurrence and death, independently of tumor grade, stage, and lymph-node status. Patients with transitional-cell carcinoma confirmed to the bladder that demonstrates nuclear p53 reactivity should be considered for protocols of adjuvant treatment.

摘要

背景

我们之前通过免疫组织化学分析证明,p53蛋白的核内积聚与p53基因突变之间存在密切关联。本研究的目的是确定膀胱移行细胞癌中p53核内积聚与肿瘤进展之间的关系。

方法

对243例行根治性膀胱切除术患者的膀胱移行细胞癌组织标本(分期从Pa期,非浸润性疾病,到P4期,直接侵犯相邻器官或结构的疾病)进行p53蛋白的免疫组织化学检测。然后分析核p53反应性与复发时间和总生存期的关系。

结果

核p53的检测与膀胱癌复发风险增加显著相关(P < 0.001),与总生存期缩短显著相关(P < 0.001)。在局限于膀胱的癌症患者中,五年时未检测到核p53反应性的P1、P2和P3a期肿瘤的复发率分别为7%、12%和11%,而有p53免疫反应性的肿瘤复发率分别为62%、56%和80%。当研究肿瘤细胞核中p53的有无与总生存期的关系时,也得到了类似结果。在根据分级、病理分期和淋巴结状态进行分层的多变量分析中,核p53状态是复发和总生存期的独立预测因素(在局限于膀胱的癌症中,是唯一的独立预测因素)(P < 0.001)。

结论

在局限于膀胱的移行细胞癌患者中,通过免疫组织化学方法检测到肿瘤细胞核中p53积聚预示复发和死亡风险显著增加,且独立于肿瘤分级、分期和淋巴结状态。对于经证实局限于膀胱且显示核p53反应性的移行细胞癌患者,应考虑给予辅助治疗方案。

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