Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States.
National Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, Maryland 20850, United States.
ACS Chem Biol. 2022 Dec 16;17(12):3290-3297. doi: 10.1021/acschembio.2c00710. Epub 2022 Dec 5.
Autophagy is a conserved metabolic pathway that is central to many diseases. Recently, there has been a lot of interest in targeting autophagy with small molecule inhibitors as a possible therapeutic strategy. However, many of the compounds used for autophagy are nonselective. Here, we explored the inhibition of autophagy in pancreatic cancer cells using established selective small molecule inhibitors and discovered an unexpected link between the autophagy pathway and progression through the cell cycle. Our findings revealed that treatments with inhibitors that have different autophagy pathway targets block cell replication and activate other metabolic pathways to compensate for the blockade in autophagy. An unbiased screen looking for known drugs that might synergize with autophagy inhibition revealed new combination treatments that might provide a blueprint for therapeutic approaches to pancreatic cancer. The drugs quizartinib and THZ1 showed a strong synergistic effect in pancreatic cells with autophagy inhibition.
自噬是一种保守的代谢途径,对许多疾病都很重要。最近,人们对使用小分子抑制剂靶向自噬作为一种潜在的治疗策略产生了浓厚的兴趣。然而,许多用于自噬的化合物是非选择性的。在这里,我们使用已建立的选择性小分子抑制剂来探索胰腺癌细胞中自噬的抑制,并发现自噬途径与细胞周期通过之间存在意外的联系。我们的研究结果表明,用不同自噬途径靶点的抑制剂处理会阻断细胞复制,并激活其他代谢途径来补偿自噬的阻断。一项寻找可能与自噬抑制协同作用的已知药物的无偏见筛选揭示了新的联合治疗方法,为胰腺癌的治疗方法提供了蓝图。药物 quizartinib 和 THZ1 在具有自噬抑制的胰腺细胞中表现出强烈的协同作用。