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萝卜硫素与 CB-5083 协同作用并抑制 CB-5083 耐药的 HCT116 细胞集落形成。

Sulforaphane is Synergistic with CB-5083 and Inhibits Colony Formation of CB-5083-Resistant HCT116 Cells.

机构信息

Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

NExT Program Support, Applied/Developmental Research Directorate, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.

出版信息

ChemMedChem. 2022 Jun 3;17(11):e202200030. doi: 10.1002/cmdc.202200030. Epub 2022 Apr 22.

Abstract

Human p97 is a potential drug target in oncology. Mutation-driven drug resistance is an obstacle to the long-term efficacy of targeted therapy. We found that the ATPase activity for one of the CB-5083-resistant p97 mutants was reduced, which also attenuated the degradation of K48 ubiquitinated proteins in cells. To understand how p97 mutant cells with significantly reduced ATPase activity can still grow, we discovered reduced levels of CHOP and NF-κB activation in the p97 mutant cells and these cellular changes can potentially protect HCT116 cells from death due to lowered p97 activity. In addition, the NF-kB inhibitor Sulforaphane reduces proliferation of CB-5083 resistant cells and acts synergistically with CB-5083 to block proliferation of the parental HCT116 cells. The combination of Sulforaphane and CB-5083 may be a useful treatment strategy to combat CB-5083 resistance.

摘要

人类 p97 是肿瘤学中的一个潜在药物靶点。突变驱动的耐药性是靶向治疗长期疗效的障碍。我们发现,一种对 CB-5083 耐药的 p97 突变体的 ATP 酶活性降低,这也减弱了细胞中 K48 泛素化蛋白的降解。为了了解具有显着降低的 ATP 酶活性的 p97 突变细胞如何仍能生长,我们发现 p97 突变细胞中的 CHOP 和 NF-κB 激活水平降低,这些细胞变化可能潜在地保护 HCT116 细胞免于因 p97 活性降低而死亡。此外,NF-κB 抑制剂萝卜硫素降低 CB-5083 耐药细胞的增殖,并与 CB-5083 协同作用以阻断亲本 HCT116 细胞的增殖。萝卜硫素和 CB-5083 的联合使用可能是对抗 CB-5083 耐药性的有效治疗策略。

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