Selivanova G, Kawasaki T, Ryabchenko L, Wiman K G
Microbiology and Tumor Biology Center, Karolinska Institute, Stockholm, Sweden.
Semin Cancer Biol. 1998;8(5):369-78. doi: 10.1006/scbi.1998.0099.
The specific DNA binding activity of p53 is crucial for its tumor suppression function. Naturally occurring mutant forms of p53 are deficient for specific DNA binding. However, several studies have indicated that their specific DNA binding can be reactivated. Short peptides derived from the p53 C-terminus can reactivate at least some mutant p53 proteins and trigger a p53-dependent biological response. These results may provide the basis for the design of p53-reactivating anti-cancer drugs.
p53的特异性DNA结合活性对其肿瘤抑制功能至关重要。p53的天然突变形式缺乏特异性DNA结合能力。然而,多项研究表明其特异性DNA结合可被重新激活。源自p53 C末端的短肽可重新激活至少部分突变型p53蛋白并引发p53依赖性生物学反应。这些结果可能为设计p53重新激活抗癌药物提供依据。