Afsharmoghadam Noushin, Haghighatian Zahra, Mazdak Hamid, Mirkheshti Nooshin, Mehrabi Koushki Razieh, Alavi Sayyed Ali
Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran. Email:
Asian Pac J Cancer Prev. 2017 Dec 28;18(12):3225-3230. doi: 10.22034/APJCP.2017.18.12.3225.
Purpose: Curcumin (Cur), a herbal ingredient with anticancer properties, has been shown to inhibit growth of malignant cells in vivo and in vitro. However, studies on combination therapy of Cur with chemotherapeutic drugs have been limited. Here, effects of Cur on the cytotoxicity of 5-Fluorouracil (FU) were investigated with epithelial bladder cancer cells (EJ138) in vitro. Methods: EJ138 cells were treated with 5 and 15 μM of Cur and/ or 100 μM of FU. Cell viability was measured by sulforhodamine B colorimetric assay. The glucose concentration as an index of cell metabolism was evaluated by an enzymatic method. Total oxidant and antioxidant capacities were estimated by the ferrous oxidation-xylenol (FOX1) method and ferric reducing antioxidant power assay (FRAP), respectively. Results: Combination of 5 μM Cur with FU significantly reduced its cytotoxicity in EJ138 cells, while 15 μM Cur caused an opposite increase. Significant increase in glucose concentration at 24 h and decrease in the FRAP value at 48 h incubation was observed in cells treated with FU in combination with Cur. There were no significant changes in total oxidant capacity with the combination therapy. Conclusion: Our findings suggest a crucial role of Cur concentration in regulating chemotherapeutic agent-induced cytotoxicity. Further investigations are needed to understand the precise mechanisms of action of Cur and determine appropriate doses with combination therapy for clinical application against human cancers.
姜黄素(Cur)是一种具有抗癌特性的草药成分,已被证明在体内和体外均可抑制恶性细胞的生长。然而,关于Cur与化疗药物联合治疗的研究有限。在此,我们在体外研究了Cur对5-氟尿嘧啶(FU)对上皮性膀胱癌细胞(EJ138)细胞毒性的影响。方法:用5和15 μM的Cur和/或100 μM的FU处理EJ138细胞。通过磺基罗丹明B比色法测定细胞活力。通过酶法评估作为细胞代谢指标的葡萄糖浓度。分别通过亚铁氧化-二甲苯酚(FOX1)法和铁还原抗氧化能力测定法(FRAP)评估总氧化剂和抗氧化剂能力。结果:5 μM的Cur与FU联合使用可显著降低其对EJ138细胞的细胞毒性,而15 μM的Cur则产生相反的效果。在用FU与Cur联合处理的细胞中,在孵育24小时时观察到葡萄糖浓度显著增加,在48小时时FRAP值降低。联合治疗对总氧化剂能力没有显著变化。结论:我们的研究结果表明Cur浓度在调节化疗药物诱导的细胞毒性中起关键作用。需要进一步研究以了解Cur的精确作用机制,并确定联合治疗用于临床治疗人类癌症的合适剂量。