Effects of thymoquinone and the curcumin analog EF-24 on the activity of the enzyme paraoxonase-1 in human glioblastoma cells U87MG.

IF 5.6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Enzyme Inhibition and Medicinal Chemistry Pub Date : 2024-12-01 Epub Date: 2024-06-12 DOI:10.1080/14756366.2024.2339901
Ender Simsek, Asuman Sunguroglu, Ahmet Kilic, Nurbanu Özgültekin, O Ozensoy Guler
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Abstract

The spices and aromatic herbs were used not only in cooking to add flavour and smell to dishes but also for medicinal use. Nigella sativa, also called black cumin, is one of the species that contains an important bioactive component, thymoquinone (TQ), which has antioxidant, anti-inflammatory, antimicrobial, and antidiabetic effects. Curcuma longa, which also includes curcumin, has numerous anti-cancer properties. However, the bioavailability of curcumin is lower than that of its analogs. An analog of curcumin (EF-24), which has better bioavailability than curcumin, is capable of exerting a high anti-cancer effect. In our study, we determined the effects of PON1 enzyme activity on the proliferation and aggressiveness of glioblastoma cancer treated with TQ and EF-24 from lysates of the glioblastoma cell line U87MG. The results were determined as increased PON1 activity after treatment with TQ and EF-24 in the U87MG cell line (p < 0.0001).

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胸腺醌和姜黄素类似物 EF-24 对人胶质母细胞瘤细胞 U87MG 中副氧合酶-1 活性的影响。
香料和芳香草药不仅用于烹饪,为菜肴增添风味和香气,还可用于药用。Nigella sativa(又称黑孜然)是其中一种含有重要生物活性成分胸腺醌(TQ)的香料,具有抗氧化、抗炎、抗菌和抗糖尿病作用。姜黄也包括姜黄素,具有多种抗癌特性。然而,姜黄素的生物利用率低于其类似物。姜黄素的类似物(EF-24)比姜黄素具有更好的生物利用度,能够发挥很强的抗癌效果。在我们的研究中,我们从胶质母细胞瘤细胞系 U87MG 的裂解物中测定了 PON1 酶活性对使用 TQ 和 EF-24 治疗的胶质母细胞瘤的增殖和侵袭性的影响。结果表明,经 TQ 和 EF-24 处理后,U87MG 细胞系的 PON1 活性增加(p
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来源期刊
CiteScore
10.30
自引率
10.70%
发文量
195
审稿时长
4-8 weeks
期刊介绍: Journal of Enzyme Inhibition and Medicinal Chemistry publishes open access research on enzyme inhibitors, inhibitory processes, and agonist/antagonist receptor interactions in the development of medicinal and anti-cancer agents. Journal of Enzyme Inhibition and Medicinal Chemistry aims to provide an international and interdisciplinary platform for the latest findings in enzyme inhibition research. The journal’s focus includes current developments in: Enzymology; Cell biology; Chemical biology; Microbiology; Physiology; Pharmacology leading to drug design; Molecular recognition processes; Distribution and metabolism of biologically active compounds.
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