Ozçelik H, Mousses S, Andrulis I L
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, and Departments of Cellular and Molecular Pathology, Toronto, Ontario M5G 1X5, Canada.
Clin Cancer Res. 1995 Aug;1(8):907-12.
Recently, several groups have isolated a cell cycle inhibitor gene (CIP1/WAF1) that is highly induced by wild-type, but not mutant forms of the p53 tumor suppressor. To test the hypothesis that p53 regulates CIP1/WAF1 expression in vivo, we evaluated CIP1/WAF1 mRNA expression levels in breast carcinomas from individuals with axillary node-negative disease with and without p53 mutations using quantitative reverse transcription-PCR. The data demonstrate that there is a strong negative correlation between the presence of p53 mutations and CIP1/WAF1 expression, suggesting that p53 mutations may reduce its ability to induce CIP1/WAF1 in vivo. In this study we observed tumors with low levels of CIP1/WAF1 mRNA in which there were no detectable p53 mutations. Determination of the CIP1/WAF1 levels in such specimens may provide a complementary strategy for analyzing the effects of p53 defects and/or may suggest the presence of alterations (such as coding mutations outside the conserved regions, promoter mutations, etc.) that may be missed by standard techniques.
最近,几个研究小组分离出了一种细胞周期抑制基因(CIP1/WAF1),该基因在野生型p53肿瘤抑制因子作用下会高度表达,而在其突变形式作用下则不会。为了验证p53在体内调节CIP1/WAF1表达的假说,我们使用定量逆转录PCR评估了腋窝淋巴结阴性乳腺癌患者中有无p53突变时CIP1/WAF1 mRNA的表达水平。数据表明,p53突变的存在与CIP1/WAF1表达之间存在强烈的负相关,这表明p53突变可能会降低其在体内诱导CIP1/WAF1的能力。在本研究中,我们观察到CIP1/WAF1 mRNA水平较低的肿瘤,其中未检测到p53突变。测定此类标本中的CIP1/WAF1水平可能为分析p53缺陷的影响提供一种补充策略,和/或可能提示存在标准技术可能遗漏的改变(如保守区域外的编码突变、启动子突变等)。