Asker C, Wiman K G, Selivanova G
Cancer Center Karolinska, Karolinska Institute, Stockholm, SE-171 77, Sweden.
Biochem Biophys Res Commun. 1999 Nov;265(1):1-6. doi: 10.1006/bbrc.1999.1446.
p53 acts as a potent tumor suppressor largely through its ability to induce cell death by apoptosis. Diverse cellular stress conditions, e.g., DNA damage, hypoxia, and oncogene activation, trigger p53-dependent apoptosis. ARF is a 14-kDa protein encoded by an alternative reading frame within the human INK4a locus that also encodes the p16 protein. ARF induces p53 in response to oncogene activation by preventing its degradation. This ensures the elimination of emerging tumor cells by p53-dependent apoptosis. p53 promotes apoptosis through multiple mechanisms, including transactivation of specific target genes, down-regulation of a distinct set of genes, and transcription-independent mechanisms. This may explain the frequent inactivation of ARF/p53 rather than downstream effectors during tumor development.
p53主要通过其诱导细胞凋亡导致细胞死亡的能力,发挥强大的肿瘤抑制作用。多种细胞应激条件,如DNA损伤、缺氧和癌基因激活,均可触发p53依赖的细胞凋亡。ARF是一种由人类INK4a基因座内的一个可读框编码的14 kDa蛋白,该基因座也编码p16蛋白。ARF通过阻止p53降解来响应癌基因激活,进而诱导p53表达。这确保了通过p53依赖的细胞凋亡消除新出现的肿瘤细胞。p53通过多种机制促进细胞凋亡,包括特定靶基因的反式激活、一组不同基因的下调以及转录非依赖机制。这可能解释了在肿瘤发生过程中ARF/p53而非下游效应器频繁失活的现象。