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光动力疗法和化学动力疗法中谷胱甘肽消耗的新策略:综述

Novel strategies of glutathione depletion in photodynamic and chemodynamic therapy: A review.

作者信息

Wolny Daniel, Stojko Mateusz, Zajdel Alicja

机构信息

Department of Biopharmacy, Faculty of Pharmaceutical Sciences, Medical University of Silesia, Sosnowiec, Poland.

Centre of Polymer and Carbon Materials, Polish Academy of Sciences, Zabrze, Poland.

出版信息

Adv Clin Exp Med. 2024 Sep 20. doi: 10.17219/acem/191025.

Abstract

Cancer remains a health problem worldwide; therefore, developing new therapies to increase the effectiveness of anticancer treatments is necessary. Two such methods are photodynamic therapy (PDT) and chemodynamic therapy (CDT). The intensive growth and increased metabolism of tumors lead to elevated levels of reactive oxygen species (ROS) within cancer cells. These cells develop several antioxidant mechanisms to protect them from this oxidative stress. Antioxidants also make tumors more resistant to chemotherapy and radiation. Glutathione (GSH) is an important and the most abundant endogenous cellular antioxidant. Photodynamic therapy and CDT are new methods that are based on the production of ROS,‑ therefore increasing oxidative stress in cancer cells. A significant problem with these therapies is the increased GSH levels, which is an adaptation of cancer cells to augmented metabolic processes. This paper presents various GSH depletion strategies that are used to improve PDT and CDT. While the main goal of GSH depletion in both PDT and CDT is to prevent its interaction with the ROS generated by these therapies, it should be remembered that the reduction of its level itself may initiate pathways leading to cancer cell death.

摘要

癌症仍然是一个全球性的健康问题;因此,开发新的疗法以提高抗癌治疗的有效性是必要的。光动力疗法(PDT)和化学动力疗法(CDT)就是这样的两种方法。肿瘤的快速生长和新陈代谢增加导致癌细胞内活性氧(ROS)水平升高。这些细胞发展出几种抗氧化机制来保护它们免受这种氧化应激。抗氧化剂也使肿瘤对化疗和放疗更具抗性。谷胱甘肽(GSH)是一种重要且最丰富的内源性细胞抗氧化剂。光动力疗法和化学动力疗法是基于ROS产生的新方法,因此会增加癌细胞中的氧化应激。这些疗法的一个重大问题是GSH水平升高,这是癌细胞对增强的代谢过程的一种适应。本文介绍了用于改善光动力疗法和化学动力疗法的各种GSH消耗策略。虽然在光动力疗法和化学动力疗法中消耗GSH的主要目标是防止其与这些疗法产生ROS相互作用,但应该记住,其水平的降低本身可能会启动导致癌细胞死亡的途径。

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