Lee Ko-Chao, Wu Kuen-Lin, Chang Shun-Fu, Chang Hsin-I, Chen Cheng-Nan, Chen Yih-Yuan
Division of Colorectal Surgery, Department of Surgery, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Department of Medical Research and Development, Chang Gung Memorial Hospital Chiayi Branch, Chiayi 613, Taiwan.
Antioxidants (Basel). 2022 Oct 19;11(10):2057. doi: 10.3390/antiox11102057.
Ginger extracts have been shown to have health-promoting pharmacological activity and beneficial effects, including antioxidant and anticancer properties. The extraction of ginger by natural deep eutectic solvents (NaDES) has been shown to enhance bioactivity, but the cytotoxicity of NaDES extracts needs to be further determined. Signaling through the CXC chemokine receptor 4 (CXCR4) expressed on colorectal cancer (CRC) cells has a pivotal role in tumor cell chemosensitivity. Oxaliplatin is a third-generation platinum compound used as an effective chemotherapeutic drug for CRC treatment. However, whether ginger extract and oxaliplatin could induce a synergistic cytotoxic effect in oxaliplatin-resistant CRC cells through modulating CXCR4 expression is not known. In this study, oxaliplatin-resistant HCT-116 (HCT-116/R) cells were generated first. Ginger was extracted using the NaDES mixture betaine/lactate/water (1:2:2.5). Lactobacillus reuteri fermentation of NaDES-ginger extract increased the total polyphenol content (12.42 mg gallic acid/g in non-fermented NaDES-ginger extract and 23.66 mg gallic acid/g in fermented NaDES-ginger extract). It also increased the antioxidant activity by about 20−30% compared to non-fermented NaDES-ginger extract. In addition, it achieved low cytotoxicity to normal colonic mucosal cells and enhanced the anticancer effect on HCT-116/R cells. On the other hand, the inhibition of NF-κB activation by fermented NaDES-ginger extract significantly decreased the CXCR4 expression (p < 0.05) in HCT-116/R cells. The inactivation of NF-κB by pharmacological inhibitor pyrrolidine dithiocarbamate further enhanced the fermented NaDES-ginger extract-reduced CXCR4 expression levels (p < 0.05). Moreover, fermented NaDES-ginger extract could synergistically increase the cytotoxicity of oxaliplatin by inhibiting CXCR4 expression and inactivating NF-κB, resulting in HCT-116/R cell death. These findings demonstrate that fermented NaDES-ginger extract reduces the NF-kB-mediated activation of CXCR4 and enhances oxaliplatin-induced cytotoxicity in oxaliplatin-resistant CRC cells.
姜提取物已被证明具有促进健康的药理活性和有益作用,包括抗氧化和抗癌特性。天然深共熔溶剂(NaDES)提取姜已被证明可增强生物活性,但NaDES提取物的细胞毒性需要进一步确定。通过结肠直肠癌(CRC)细胞上表达的CXC趋化因子受体4(CXCR4)发出的信号在肿瘤细胞化学敏感性中起关键作用。奥沙利铂是一种第三代铂化合物,用作治疗CRC的有效化疗药物。然而,姜提取物和奥沙利铂是否能通过调节CXCR4表达在耐奥沙利铂的CRC细胞中诱导协同细胞毒性作用尚不清楚。在本研究中,首先产生了耐奥沙利铂的HCT-116(HCT-116/R)细胞。使用NaDES混合物甜菜碱/乳酸/水(1:2:2.5)提取姜。罗伊氏乳杆菌发酵NaDES-姜提取物增加了总多酚含量(未发酵的NaDES-姜提取物中为12.42mg没食子酸/g,发酵的NaDES-姜提取物中为23.66mg没食子酸/g)。与未发酵的NaDES-姜提取物相比,其抗氧化活性也提高了约20%-30%。此外,它对正常结肠黏膜细胞的细胞毒性较低,并增强了对HCT-116/R细胞的抗癌作用。另一方面,发酵的NaDES-姜提取物对NF-κB激活的抑制作用显著降低了HCT-116/R细胞中CXCR4的表达(p<0.05)。用药物抑制剂吡咯烷二硫代氨基甲酸盐使NF-κB失活进一步增强了发酵的NaDES-姜提取物降低的CXCR4表达水平(p<0.05)。此外,发酵的NaDES-姜提取物可通过抑制CXCR4表达和使NF-κB失活协同增加奥沙利铂的细胞毒性,导致HCT-116/R细胞死亡。这些发现表明,发酵的NaDES-姜提取物降低了NF-κB介导的CXCR4激活,并增强了奥沙利铂在耐奥沙利铂的CRC细胞中诱导的细胞毒性。