Jeong Soyeon, Kim Bu Gyeom, Kim Dae Yeong, Kim Bo Ram, Kim Jung Lim, Park Seong Hye, Na Yoo Jin, Jo Min Jee, Yun Hye Kyeong, Jeong Yoon A, Kim Hong Jun, Lee Sun Il, Kim Han Do, Kim Dae Hyun, Oh Sang Cheul, Lee Dae-Hee
Division of Oncology/Hematology, Department of Internal Medicine, Korea University Guro Hospital, 148, Gurodong-gil, Guro-gu, Seoul 08308, Korea.
Graduate School of Medicine, College of Medicine, Korea University, Seoul 08308, Korea.
Cancers (Basel). 2019 Jun 5;11(6):781. doi: 10.3390/cancers11060781.
Although oxaliplatin is an effective chemotherapeutic drug for colorectal cancer (CRC) treatment, patients often develop resistance to it. Therefore, a new strategy for CRC treatment is needed. The purpose of this study was to determine the effect of cannabidiol (CBD), one of the components of the cannabis plant, in overcoming oxaliplatin resistance in CRC cells. We established oxaliplatin-resistant cell lines, DLD-1 R and colo205 R, in CRC DLD-1 and colo205 cells. Autophagic cell death was induced when oxaliplatin-resistant cells were treated with both oxaliplatin and CBD. Additionally, phosphorylation of nitric oxide synthase 3 (NOS3) was increased in oxaliplatin-resistant cells compared to that in parent cells. Combined treatment with oxaliplatin and CBD reduced phospho-NOS3 levels and nitric oxide (NO) production and resulted in the production of reactive oxygen species (ROS) by reducing the levels of superoxide dismutase 2, an antioxidant present in the mitochondria, causing mitochondrial dysfunction. Taken together, these results suggest that elevated phosphorylation of NOS3 is essential for oxaliplatin resistance. The combination of oxaliplatin and CBD decreased NOS3 phosphorylation, which resulted in autophagy, by inducing the overproduction of ROS through mitochondrial dysfunction, thus overcoming oxaliplatin resistance.
尽管奥沙利铂是一种用于治疗结直肠癌(CRC)的有效化疗药物,但患者常常会对其产生耐药性。因此,需要一种新的CRC治疗策略。本研究的目的是确定大麻植物成分之一的大麻二酚(CBD)在克服CRC细胞对奥沙利铂耐药性方面的作用。我们在CRC DLD-1和colo205细胞中建立了奥沙利铂耐药细胞系,即DLD-1 R和colo205 R。当用奥沙利铂和CBD处理奥沙利铂耐药细胞时,会诱导自噬性细胞死亡。此外,与亲本细胞相比,奥沙利铂耐药细胞中一氧化氮合酶3(NOS3)的磷酸化增加。奥沙利铂和CBD联合处理降低了磷酸化NOS3水平和一氧化氮(NO)的产生,并通过降低线粒体中存在的抗氧化剂超氧化物歧化酶2的水平导致活性氧(ROS)的产生,从而引起线粒体功能障碍。综上所述,这些结果表明NOS3磷酸化升高对于奥沙利铂耐药至关重要。奥沙利铂和CBD的联合使用降低了NOS3磷酸化,通过线粒体功能障碍诱导ROS的过量产生,从而导致自噬,进而克服了奥沙利铂耐药性。