Fox S B, Persad R A, Royds J, Kore R N, Silcocks P B, Collins C C
Department of Pathology, University of Sheffield Medical School, United Kingdom.
J Urol. 1993 Aug;150(2 Pt 1):490-4. doi: 10.1016/s0022-5347(17)35533-7.
Forty-five stage A1 prostatic adenocarcinomas from patients with a mean age of 65 years were examined for p53 and c-myc expression to determine whether the presence or absence of these proteins could predict tumor behavior. Thirteen (6 of 45) and seventy-three percent (33 of 45) of cases were respectively p53 and c-myc positive. p53 expression was confirmed to the tumor cells, whereas c-myc immunoreactivity was present in both malignant and surrounding hyperplastic prostate. Statistical analysis showed that although p53 and c-myc expression were positively correlated, expression of neither nuclear protein was associated with a significantly worse survival (p53: p = 0.0791 exact two-tailed; c-myc: p = 0.738 exact two-tailed). These results suggest that while both p53 and c-myc may play a role in prostatic carcinogenesis, neither appears to identify patients who may benefit from treatment in stage A disease.
对45例平均年龄65岁患者的A1期前列腺腺癌进行p53和c-myc表达检测,以确定这些蛋白的有无能否预测肿瘤行为。45例病例中分别有13例(45例中的6例)和73%(45例中的33例)为p53和c-myc阳性。p53表达在肿瘤细胞中得到证实,而c-myc免疫反应性在恶性及周围增生性前列腺组织中均有存在。统计分析表明,虽然p53和c-myc表达呈正相关,但两种核蛋白的表达均与生存率显著降低无关(p53:精确双侧检验p = 0.0791;c-myc:精确双侧检验p = 0.738)。这些结果表明,虽然p53和c-myc可能都在前列腺癌发生中起作用,但两者似乎都无法识别出可能从A期疾病治疗中获益的患者。