Department of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27858, USA.
Department of Biomedical and Neuromotor Sciences, Università di Bologna, 40126 Bologna, Italy.
Biomolecules. 2022 Feb 8;12(2):276. doi: 10.3390/biom12020276.
Pancreatic ductal adenocarcinoma (PDAC) is the most common form of pancreatic cancer. In ~75% of PDAC, the tumor suppressor gene is mutated. Novel approaches to treat cancer involve compounds called mutant TP53 reactivators. They interact with mutant TP53 proteins and restore some of their growth suppressive properties, but they may also interact with other proteins, e.g., TP63 and TP73. We examined the ability of the TP53 reactivator APR-246 to interact with eleven modified berberine compounds (NAX compounds) in the presence and absence of WT-TP53 in two PDAC cell lines: the MIA-PaCa-2, which has gain of function (GOF) TP53 mutations on both alleles, and PANC-28, which lacks expression of the WT TP53 protein. Our results indicate the TP53 reactivator-induced increase in therapeutic potential of many modified berberines.
胰腺导管腺癌 (PDAC) 是最常见的胰腺癌形式。在大约 75%的 PDAC 中,肿瘤抑制基因发生了突变。治疗癌症的新方法涉及一种称为突变 TP53 激活剂的化合物。它们与突变的 TP53 蛋白相互作用,恢复了其部分生长抑制特性,但它们也可能与其他蛋白质相互作用,例如 TP63 和 TP73。我们在两种 PDAC 细胞系中研究了 TP53 激活剂 APR-246 在 WT-TP53 存在和不存在的情况下与 11 种修饰小檗碱化合物 (NAX 化合物) 相互作用的能力:MIA-PaCa-2,其两个等位基因上都有功能获得 (GOF) TP53 突变,而 PANC-28 则缺乏 WT TP53 蛋白的表达。我们的结果表明,TP53 激活剂诱导了许多修饰小檗碱的治疗潜力的增加。