Vojtesek B, Kovarik J, Dolezalova H, Nenutil R, Havlis P, Brentani R R, Lane D P
Department of Cellular and Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech.
Br J Cancer. 1995 Jun;71(6):1253-6. doi: 10.1038/bjc.1995.242.
We analysed antibodies specific for human p53 in sera from primary breast cancer patients using three different immunoassays and we related these results to the p53 level in tumour tissue detected by immunohistochemistry. Only 44% (11/25) of apparently enzyme-linked immunosorbent assay (ELISA)-positive sera were from patients with a high level of p53 protein in more than 50% of their tumour cells. Surprisingly, 36% (9/25) of the sera originated from patients with no detectable p53 protein at all. Immunoprecipitation data suggested that the reason for this discrepancy is that at least some of the antibodies detected as positive in the ELISA in these sera from patients with clinical stage I and stage II breast cancers may be induced by immunogens other than p53 protein. Many of these reactions give apparently positive signals in a variety of p53 assays, and very stringent analysis is required to avoid possible misinterpretation of these responses as a p53-specific B-cell response in human cancer patients.
我们使用三种不同的免疫测定法分析了原发性乳腺癌患者血清中针对人p53的特异性抗体,并将这些结果与通过免疫组织化学检测到的肿瘤组织中的p53水平相关联。在明显酶联免疫吸附测定(ELISA)阳性的血清中,只有44%(11/25)来自超过50%肿瘤细胞中p53蛋白水平较高的患者。令人惊讶的是,36%(9/25)的血清来自完全检测不到p53蛋白的患者。免疫沉淀数据表明,这种差异的原因是,在这些临床I期和II期乳腺癌患者的血清中,至少有一些在ELISA中检测为阳性的抗体可能是由p53蛋白以外的免疫原诱导产生的。许多这些反应在各种p53检测中都给出明显的阳性信号,因此需要非常严格的分析,以避免将这些反应误解释为人类癌症患者中p53特异性B细胞反应。