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金丝桃素在光照与黑暗中:同一硬币的两面

Hypericin in the Light and in the Dark: Two Sides of the Same Coin.

作者信息

Jendželovská Zuzana, Jendželovský Rastislav, Kuchárová Barbora, Fedoročko Peter

机构信息

Department of Cellular Biology, Faculty of Science, Pavol Jozef Šafárik University in Košice Košice, Slovakia.

出版信息

Front Plant Sci. 2016 May 6;7:560. doi: 10.3389/fpls.2016.00560. eCollection 2016.

Abstract

Hypericin (4,5,7,4',5',7'-hexahydroxy-2,2'-dimethylnaphtodianthrone) is a naturally occurring chromophore found in some species of the genus Hypericum, especially Hypericum perforatum L. (St. John's wort), and in some basidiomycetes (Dermocybe spp.) or endophytic fungi (Thielavia subthermophila). In recent decades, hypericin has been intensively studied for its broad pharmacological spectrum. Among its antidepressant and light-dependent antiviral actions, hypericin is a powerful natural photosensitizer that is applicable in the photodynamic therapy (PDT) of various oncological diseases. As the accumulation of hypericin is significantly higher in neoplastic tissue than in normal tissue, it can be used in photodynamic diagnosis (PDD) as an effective fluorescence marker for tumor detection and visualization. In addition, light-activated hypericin acts as a strong pro-oxidant agent with antineoplastic and antiangiogenic properties, since it effectively induces the apoptosis, necrosis or autophagy of cancer cells. Moreover, a strong affinity of hypericin for necrotic tissue was discovered. Thus, hypericin and its radiolabeled derivatives have been recently investigated as potential biomarkers for the non-invasive targeting of tissue necrosis in numerous disorders, including solid tumors. On the other hand, several light-independent actions of hypericin have also been described, even though its effects in the dark have not been studied as intensively as those of photoactivated hypericin. Various experimental studies have revealed no cytotoxicity of hypericin in the dark; however, it can serve as a potential antimetastatic and antiangiogenic agent. On the contrary, hypericin can induce the expression of some ABC transporters, which are often associated with the multidrug resistance (MDR) of cancer cells. Moreover, the hypericin-mediated attenuation of the cytotoxicity of some chemotherapeutics was revealed. Therefore, hypericin might represent another St. John's wort metabolite that is potentially responsible for negative herb-drug interactions. The main aim of this review is to summarize the benefits of photoactivated and non-activated hypericin, mainly in preclinical and clinical applications, and to uncover the "dark side" of this secondary metabolite, focusing on MDR mechanisms.

摘要

金丝桃素(4,5,7,4',5',7'-六羟基-2,2'-二甲基萘并二蒽酮)是一种天然存在的发色团,存在于金丝桃属的某些物种中,尤其是贯叶连翘(圣约翰草),以及一些担子菌(皮伞属物种)或内生真菌(嗜热栖热放线菌)中。近几十年来,人们对金丝桃素广泛的药理作用进行了深入研究。在其抗抑郁和光依赖性抗病毒作用中,金丝桃素是一种强大的天然光敏剂,可应用于各种肿瘤疾病的光动力疗法(PDT)。由于金丝桃素在肿瘤组织中的积累明显高于正常组织,它可作为一种有效的荧光标记物用于光动力诊断(PDD),以检测和可视化肿瘤。此外,光激活的金丝桃素作为一种强大的促氧化剂,具有抗肿瘤和抗血管生成特性,因为它能有效诱导癌细胞的凋亡、坏死或自噬。此外,还发现金丝桃素对坏死组织具有很强的亲和力。因此,金丝桃素及其放射性标记衍生物最近被研究作为多种疾病(包括实体瘤)中组织坏死非侵入性靶向的潜在生物标志物。另一方面,尽管金丝桃素在黑暗中的作用没有像光激活的金丝桃素那样得到深入研究,但也有一些关于其非光依赖性作用的描述。各种实验研究表明,金丝桃素在黑暗中没有细胞毒性;然而,它可作为一种潜在的抗转移和抗血管生成剂。相反,金丝桃素可诱导一些ABC转运蛋白的表达,这些转运蛋白通常与癌细胞的多药耐药性(MDR)有关。此外,还发现金丝桃素介导了一些化疗药物细胞毒性的减弱。因此,金丝桃素可能代表了圣约翰草的另一种代谢产物,它可能是导致不良草药-药物相互作用的潜在原因。本综述的主要目的是总结光激活和未激活的金丝桃素的益处,主要是在临床前和临床应用方面,并揭示这种次生代谢产物的“阴暗面”,重点关注多药耐药机制。

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Photoactivated hypericin is not genotoxic.光活化金丝桃素无基因毒性。
Gen Physiol Biophys. 2016 Apr;35(2):223-30. doi: 10.4149/gpb_2015045. Epub 2016 Feb 18.

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