Sullivan A, Lu X
Ludwig Institute for Cancer Research, University College London, 91 Riding House Street, London W1W 7BS, UK.
Br J Cancer. 2007 Jan 29;96(2):196-200. doi: 10.1038/sj.bjc.6603525. Epub 2007 Jan 9.
The apoptosis stimulating proteins of p53 (ASPP) family consists of three members, ASPP1, ASPP2 and iASPP. They bind to proteins that are key players in controlling apoptosis (p53, Bcl-2 and RelA/p65) and cell growth (APCL, PP1). So far, the best-known function of the ASPP family members is their ability to regulate the apoptotic function of p53 and its family members, p63 and p73. Biochemical and genetic evidence has shown that ASPP1 and ASPP2 activate, whereas iASPP inhibits, the apoptotic but not the cell-cycle arrest function of p53. The p53 tumour suppressor gene, one of the most frequently mutated genes in human cancer, is capable of suppressing tumour growth through its ability to induce apoptosis or cell-cycle arrest. Thus, the ASPP family of proteins helps to determine how cells choose to die and may therefore be a novel target for cancer therapy.
p53凋亡刺激蛋白(ASPP)家族由三个成员组成,即ASPP1、ASPP2和iASPP。它们与在控制细胞凋亡(p53、Bcl-2和RelA/p65)和细胞生长(APCL、PP1)中起关键作用的蛋白质结合。到目前为止,ASPP家族成员最广为人知的功能是它们调节p53及其家族成员p63和p73凋亡功能的能力。生化和遗传学证据表明,ASPP1和ASPP2激活p53的凋亡功能而非细胞周期阻滞功能,而iASPP则抑制该功能。p53肿瘤抑制基因是人类癌症中最常发生突变的基因之一,它能够通过诱导细胞凋亡或细胞周期阻滞来抑制肿瘤生长。因此,ASPP蛋白家族有助于确定细胞如何选择死亡,可能因此成为癌症治疗的新靶点。