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一种有前景的天然蒽醌类化合物,通过光动力疗法用于癌症治疗。

A promising natural anthraquinones mediated by photodynamic therapy for anti-cancer therapy.

机构信息

Department of Clinical and Experimental Pathology, Division of General and Experimental Pathology, Wroclaw Medical University, Karola Marcinkowskiego 1 Street, 50-368, Wroclaw, Poland.

Department of Clinical and Experimental Pathology, Division of General and Experimental Pathology, Wroclaw Medical University, Karola Marcinkowskiego 1 Street, 50-368, Wroclaw, Poland.

出版信息

Phytomedicine. 2023 Oct;119:155035. doi: 10.1016/j.phymed.2023.155035. Epub 2023 Aug 16.

Abstract

BACKGROUND

Experimental studies emphasize the therapeutic potential of plant-derived photosensitizers used in photodynamic therapy. Moreover, several in vitro and in vivo research present the promising roles of less-known anthraquinones that can selectively target cancer cells and eliminate them after light irradiation. This literature review summarizes the current knowledge of chosen plant-based-photosensitizers in PDT to show the results of emodin, aloe-emodin, parietin, rubiadin, hypericin, and soranjidiol in photodynamic therapy of cancer treatment and describe the comprehensive perspective of their role as natural photosensitizers.

METHODS

Literature searches of chosen anthraquinones were conducted on PubMed.gov with keywords: "emodin", "aloe-emodin", "hypericin", "parietin", "rubiadin", "soranjidiol" with "cancer" and "photodynamic therapy".

RESULTS

According to literature data, this review concentrated on all existing in vitro and in vivo studies of emodin, aloe-emodin, parietin, rubiadin, soranjidiol used as natural photosensitizers emphasizing their effectiveness and detailed mechanism of action in anticancer therapy. Moreover, comprehensive preclinical and clinical studies on hypericin reveal that the above-described substances may be included in the phototoxic treatment of different cancers.

CONCLUSIONS

Overall, this review presented less-known anthraquinones with their promising molecular mechanisms of action. It is expected that in the future they may be used as natural PSs in cancer treatment as well as hypericin.

摘要

背景

实验研究强调了用于光动力疗法的植物源性光敏剂的治疗潜力。此外,几项体外和体内研究表明,不太为人知的蒽醌类化合物具有有前途的作用,它们可以选择性地靶向癌细胞,并在光照后消除它们。本文综述总结了选定的植物基光敏剂在 PDT 中的现有知识,以展示大黄素、芦荟大黄素、帕里汀、红紫素、金丝桃素和山奈二醇在癌症治疗的光动力疗法中的结果,并描述它们作为天然光敏剂的作用的综合观点。

方法

在 PubMed.gov 上使用关键词“大黄素”、“芦荟大黄素”、“金丝桃素”、“帕里汀”、“红紫素”和“山奈二醇”进行了选定蒽醌的文献检索,并结合“癌症”和“光动力疗法”。

结果

根据文献数据,本综述集中于所有现有的大黄素、芦荟大黄素、帕里汀、红紫素、山奈二醇作为天然光敏剂的体外和体内研究,强调了它们在癌症治疗中的有效性和详细作用机制。此外,对金丝桃素的全面临床前和临床研究表明,上述物质可能被纳入不同癌症的光毒性治疗。

结论

总的来说,本综述提出了鲜为人知的蒽醌类化合物及其有前途的分子作用机制。预计在未来,它们可能被用作癌症治疗中的天然 PSs 以及金丝桃素。

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