Efrat S, Baekkeskov S, Lane D, Hanahan D
Cold Spring Harbor Laboratory, NY 11724.
EMBO J. 1987 Sep;6(9):2699-704. doi: 10.1002/j.1460-2075.1987.tb02562.x.
The expression of p53 has been evaluated during oncogenesis of the pancreatic beta cells in transgenic mice harboring hybrid insulin-SV40 T antigen genes. Significant levels of p53 are detected in all cells expressing large T antigen. In contrast, the protein is undetectable in normal beta cells. There is a complete correspondence between the onset of expression of T antigen and the appearance of the endogenous p53 protein. In tumors, the two proteins are found in a complex. In addition, free uncomplexed T antigen is detected in every cell which expresses the transgene. These results are consistent with the participation of p53 in T antigen-induced tumorigenesis in vivo. The early appearance of p53 in all beta cells expressing large T cannot readily explain the progression of a small fraction of these cells into solid tumors.
在携带胰岛素 - SV40 T抗原基因杂交体的转基因小鼠胰腺β细胞的肿瘤发生过程中,对p53的表达进行了评估。在所有表达大T抗原的细胞中均检测到显著水平的p53。相比之下,在正常β细胞中检测不到该蛋白。T抗原表达的开始与内源性p53蛋白的出现完全一致。在肿瘤中,这两种蛋白存在于一个复合物中。此外,在每个表达转基因的细胞中都检测到了游离的未复合的T抗原。这些结果与p53参与体内T抗原诱导的肿瘤发生一致。在所有表达大T的β细胞中p53的早期出现并不能轻易解释这些细胞中的一小部分发展为实体瘤的过程。