Flaherty Daniel P, Miller Justin R, Garshott Danielle M, Hedrick Michael, Gosalia Palak, Li Yujie, Milewski Monika, Sugarman Eliot, Vasile Stefan, Salaniwal Sumeet, Su Ying, Smith Layton H, Chung Thomas D Y, Pinkerton Anthony B, Aubé Jeffrey, Callaghan Michael U, Golden Jennifer E, Fribley Andrew M, Kaufman Randal J
Delbert M. Shankel Structural Biology Center, University of Kansas Specialized Chemistry Center , 2034 Becker Drive, Lawrence, Kansas 66047, United States.
Carmen and Ann Adams Department of Pediatrics, Division of Hematology and Oncology, and the Karmanos Cancer Institute Molecular Therapeutics Group, Wayne State University , 2228 Elliman Building, 421 East Canfield, Detroit, Michigan 48201, United States.
ACS Med Chem Lett. 2014 Oct 29;5(12):1278-1283. doi: 10.1021/ml5003234. eCollection 2014 Dec 11.
Cellular proteins that fail to fold properly result in inactive or disfunctional proteins that can have toxic functions. The unfolded protein response (UPR) is a two-tiered cellular mechanism initiated by eukaryotic cells that have accumulated misfolded proteins within the endoplasmic reticulum (ER). An adaptive pathway facilitates the clearance of the undesired proteins; however, if overwhelmed, cells trigger apoptosis by upregulating transcription factors such as C/EBP-homologous protein (CHOP). A high throughput screen was performed directed at identifying compounds that selectively upregulate the apoptotic CHOP pathway while avoiding adaptive signaling cascades, resulting in a sulfonamidebenzamide chemotype that was optimized. These efforts produced a potent and selective CHOP inducer (AC = 0.8 μM; XBP1 > 80 μM), which was efficacious in both mouse embryonic fibroblast cells and a human oral squamous cell cancer cell line, and demonstrated antiproliferative effects for multiple cancer cell lines in the NCI-60 panel.
无法正确折叠的细胞蛋白质会产生无活性或功能失调的蛋白质,这些蛋白质可能具有毒性功能。未折叠蛋白反应(UPR)是真核细胞启动的一种两级细胞机制,这些细胞在内质网(ER)中积累了错误折叠的蛋白质。一种适应性途径有助于清除不需要的蛋白质;然而,如果不堪重负,细胞会通过上调转录因子如C/EBP同源蛋白(CHOP)来触发细胞凋亡。进行了一项高通量筛选,旨在鉴定能够选择性上调凋亡CHOP途径同时避免适应性信号级联反应的化合物,从而得到了一种经过优化的磺酰胺苯甲酰胺化学类型。这些努力产生了一种强效且选择性的CHOP诱导剂(AC = 0.8 μM;XBP1 > 80 μM),它在小鼠胚胎成纤维细胞和人口腔鳞状细胞癌细胞系中均有效,并在NCI-60面板中的多种癌细胞系中显示出抗增殖作用。