Labrecque S, Naor N, Thomson D, Matlashewski G
Institute of Parasitology, McGill University, Ste-Anne-de Bellevue, Quebec, Canada.
Cancer Res. 1993 Aug 1;53(15):3468-71.
Mutations in the p53 tumor suppressor gene giving rise to mutant p53 proteins are among the most common genetic alterations associated with tumor cells. Mutant p53 gene products lose the wild type ability to suppress transformation in vitro or regulate cellular gene transcription. Mutant and wild type p53 protein conformations differ and mutant p53 is often present at high levels in the tumor cell relative to the low levels found in normal cells. Despite the major advances made to characterize the structure and biology of mutant and wild type p53, the humoral immune response against mutant p53s remains to be clearly defined. In the present study we have examined the anti-p53 response from cancer patients against the native and denatured state of mutant and wild type p53. Western blot analysis, immunoprecipitation analysis, and dilution analysis demonstrate that the anti-p53 sera recognize both wild type and mutant p53 conformational and denaturation resistant epitopes. There was no evidence that the mutant p53 molecules contain dominant antigenic epitopes which are not present on the wild type p53 protein. We also demonstrate that patients with ovarian cancer are also among those which can produce anti-p53 antibodies.
p53肿瘤抑制基因发生突变产生突变型p53蛋白,是与肿瘤细胞相关的最常见基因改变之一。突变型p53基因产物丧失了在体外抑制转化或调节细胞基因转录的野生型能力。突变型和野生型p53蛋白的构象不同,相对于正常细胞中发现的低水平,突变型p53在肿瘤细胞中通常以高水平存在。尽管在表征突变型和野生型p53的结构和生物学方面取得了重大进展,但针对突变型p53的体液免疫反应仍有待明确界定。在本研究中,我们检测了癌症患者针对突变型和野生型p53的天然状态和变性状态的抗p53反应。蛋白质印迹分析、免疫沉淀分析和稀释分析表明,抗p53血清识别野生型和突变型p53的构象和抗变性表位。没有证据表明突变型p53分子含有野生型p53蛋白上不存在的显性抗原表位。我们还证明,卵巢癌患者也能够产生抗p53抗体。