化学
烟酰胺磷酸核糖转移酶
NAD+激酶
酶
癌症
癌症研究
生物化学
细胞凋亡
癌细胞
烟酰胺腺嘌呤二核苷酸
结直肠癌
烟酰胺
药理学
生长抑制
新陈代谢
腺嘌呤磷酸核糖转移酶
细胞生长
代谢途径
线粒体
毒性
糖酵解
磷酸核糖转移酶
结构-活动关系
致癌物
酶抑制剂
作者
Niccolò Paoletti,Simone Giovannuzzi,Massimiliano Gasparrini,Andrea Ammara,Zaroon Zaroon,Nadia Raffaelli,Filomena de Nigris,Paola Gratteri,Claudiu T. Supuran,Alessio Nocentini
标识
DOI:10.1021/acs.jmedchem.5c03157
摘要
We report the first dual inhibitors of the tumor-associated carbonic anhydrases (hCA IX and XII) and nicotinamide phosphoribosyltransferase (NAMPT), designed to target metabolic and pH-regulatory mechanisms critical for tumor growth and resistance. Enzymatic assays identified hits showing potent nanomolar inhibition of both targets and superior efficacy compared to reference inhibitors. Computational studies elucidated key ligand–target interactions and structure–activity relationship. In high-throughput screening cellular assays, several compounds outperformed monotherapies with strong antiproliferative effects against renal carcinoma, glioblastoma, and colorectal cancer cells under normoxic and hypoxic conditions, and limited toxicity toward nonmalignant cells. In three-dimensional (3D) spheroids, compound 45 reduced the cumulative spheroid area approximately 10-fold more than the single-target inhibitors FK866 or SLC-0111 and induced apoptosis through NAD depletion, mitochondrial dysfunction, and suppression of ERK/mTOR signaling. These results support dual hCA IX/XII–NAMPT inhibition as an effective strategy to impair tumor growth and survival under hypoxic stress.
科研通智能强力驱动
Strongly Powered by AbleSci AI