Department of Urology, Cardarelli Hospital, Campobasso, Italy.
Department of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
Amino Acids. 2021 Jan;53(1):63-72. doi: 10.1007/s00726-020-02925-1. Epub 2021 Jan 4.
Differentiation of a human aggressive PC-3 cancer cell line was obtained, in a previous investigation, by the synergic effect of α-tocopherol (α-TOC) and naringenin (NG). This combined treatment induced apoptosis and subsequent reduction of the PC-3 cell proliferation and invasion, by a pro-differentiating action. Since one of the peculiar characteristics of NG and α-TOC is their strong antioxidant activity, this study aimed to investigate their potential effect on the activity of the main enzymes involved in the antioxidant mechanism in prostate cancer cells. NG and α-TOC administered singularly or combined in the PC-3 cell line, affected the activity of several enzymes biomarkers of the cellular antioxidant activity, as well as the concentration of total glutathione (GSH + GSSG) and thiobarbituric acid reactive substances (TBARS). The combined treatment increased the TBARS levels and superoxide dismutase (SOD) activity, while decreased the glutathione S-transferase (GST), glutathione reductase (GR), and glyoxalase I (GI) activities. The results obtained indicate that a combined treatment with these natural compounds mitigated the oxidative stress in the human PC-3 cell line. In addition, a significant reduction of both ornithine decarboxylase (ODC) expression and intracellular levels of polyamines, both well-known positive regulators of cell proliferation, accompanied the reduction of oxidative stress observed in the combined α-TOC and NG treatment. Considering the established role of polyamines in cell differentiation, the synergism with NG makes α-TOC a potential drug for further study on the differentiation therapy in prostate cancer patients.
在之前的一项研究中,α-生育酚(α-TOC)和柚皮素(NG)的协同作用获得了人类侵袭性 PC-3 癌细胞系的分化。这种联合治疗通过促分化作用诱导细胞凋亡和随后降低 PC-3 细胞的增殖和侵袭。由于 NG 和 α-TOC 的一个独特特征是它们具有很强的抗氧化活性,因此本研究旨在研究它们对前列腺癌细胞中抗氧化机制主要酶活性的潜在影响。NG 和 α-TOC 单独或联合给药于 PC-3 细胞系,影响了几种酶生物标志物的活性,这些标志物是细胞抗氧化活性的指标,以及总谷胱甘肽(GSH+GSSG)和硫代巴比妥酸反应物质(TBARS)的浓度。联合治疗增加了 TBARS 水平和超氧化物歧化酶(SOD)活性,同时降低了谷胱甘肽 S-转移酶(GST)、谷胱甘肽还原酶(GR)和甘油醛 3-磷酸脱氢酶 I(GI)的活性。研究结果表明,用这些天然化合物联合治疗减轻了人 PC-3 细胞系的氧化应激。此外,联合α-TOC 和 NG 治疗观察到氧化应激减少的同时,还显著降低了鸟氨酸脱羧酶(ODC)表达和细胞内多胺水平,多胺是细胞增殖的已知正调节剂。鉴于多胺在细胞分化中的既定作用,NG 的协同作用使 α-TOC 成为进一步研究前列腺癌患者分化治疗的潜在药物。