Sharma Satish, Cwiklinski Katherine, Mahajan Supriya D, Schwartz Stanley A, Aalinkeel Ravikumar
Department of Medicine, Clinical and Translational Research Center, Division of Allergy, Immunology and Rheumatology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14203, USA.
Department of Urology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14203, USA.
Cancers (Basel). 2023 Jan 31;15(3):902. doi: 10.3390/cancers15030902.
The standard of care chemotherapy drug presently used to treat castration-resistant prostate cancer (CRPC), docetaxel (Doc), also develops chemoresistance, thereby reducing its clinical utility. Since resistance to chemotherapy drugs can be overcome by co-treatment with plant-based bio-active compounds we undertook the present study to evaluate if quercetin (Que), a flavonoid present in plants such as onions, apples, olives, and grapes can enhance the efficacy of Doc. We studied the separate and combined effects of Que and Doc at different doses and different combination approaches in two different prostate cancer cell lines, DU-145 (moderately aggressive) and PC-3 (very aggressive), and assessed the effects of these combinations on viability, proliferation, and apoptosis. Monotherapy with these drugs showed dose-dependent cytotoxicity; however, only Doc monotherapy showed a statistically significant difference in IC levels (IC = 4.05 ± 0.52 nM for PC-3 and IC = 2.26 ± 0.22 nM for DU-145). In combination treatment, we used three different treatment approaches (TAP). The concentrations and range analyzed were chosen based on the approximate cytotoxicity of 30-50% when the drugs were used individually. Our observations indicate that the most beneficial effect of the Que and Doc combination was obtained with the TAP-2 approach, which is pre-treatment with all doses of Que for 24 h followed by low doses of Doc for another 24 h. Using this approach, we observed synergism at low concentrations of Doc (0.5 and 1.0 nM) and all concentrations of Que. An additive effect was observed at moderate and high concentrations of Doc (1.5, 2.0, and 2.5 nM) and all concentrations of Que in both cell lines. The TAP-2 strategy was also helpful in overcoming Doc resistance in resistant CaP cells. In summary, Que improved the therapeutic effect of Doc in CRPC, and it is proposed that this improvement is mediated through multiple mechanisms. This study provides a novel therapeutic modality for an effective combination using Doc and Que to enhance the efficacy of Doc in an innocuous manner for Doc resistance and CRPC treatment.
目前用于治疗去势抵抗性前列腺癌(CRPC)的标准护理化疗药物多西他赛(Doc)也会产生化疗耐药性,从而降低其临床效用。由于与植物来源的生物活性化合物联合治疗可克服对化疗药物的耐药性,我们开展了本研究,以评估槲皮素(Que)——一种存在于洋葱、苹果、橄榄和葡萄等植物中的类黄酮——是否能增强多西他赛的疗效。我们在两种不同的前列腺癌细胞系DU - 145(中度侵袭性)和PC - 3(高度侵袭性)中,研究了不同剂量和不同联合方式下槲皮素和多西他赛单独及联合使用的效果,并评估了这些联合用药对细胞活力、增殖和凋亡的影响。这些药物的单药治疗均显示出剂量依赖性细胞毒性;然而,只有多西他赛单药治疗在IC水平上显示出统计学显著差异(PC - 3细胞系的IC = 4.05 ± 0.52 nM,DU - 145细胞系的IC = 2.26 ± 0.22 nM)。在联合治疗中,我们采用了三种不同的治疗方法(TAP)。所分析的浓度和范围是根据药物单独使用时约30 - 50%的近似细胞毒性来选择的。我们的观察结果表明,槲皮素和多西他赛联合使用的最有益效果是通过TAP - 2方法获得的,即先用所有剂量的槲皮素预处理24小时,然后再用低剂量的多西他赛处理24小时。采用这种方法,我们在低浓度多西他赛(0.5和1.0 nM)以及所有浓度的槲皮素下均观察到协同作用。在两种细胞系中,在中等和高浓度多西他赛(1.5、2.0和2.5 nM)以及所有浓度的槲皮素下均观察到相加作用。TAP - 2策略在克服耐药性前列腺癌细胞对多西他赛的耐药性方面也有帮助。总之,槲皮素提高了多西他赛在CRPC中的治疗效果,并且推测这种改善是通过多种机制介导的。本研究为有效联合使用多西他赛和槲皮素提供了一种新的治疗模式,以无害的方式增强多西他赛在治疗多西他赛耐药性和CRPC方面的疗效。