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黑色素瘤的氧化还原生物学与耐药性的出现。

Melanoma redox biology and the emergence of drug resistance.

机构信息

Mātai Hāora-Centre for Redox Biology and Medicine, Department of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand.

Mātai Hāora-Centre for Redox Biology and Medicine, Department of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand.

出版信息

Adv Cancer Res. 2024;162:145-171. doi: 10.1016/bs.acr.2024.06.004. Epub 2024 Jul 2.

Abstract

Melanoma is the deadliest form of skin cancer, with the loss of approximately 60,000 lives world-wide each year. Despite the development of targeted therapeutics, including compounds that have selectivity for mutant oncoproteins expressed only in cancer cells, many patients are either unresponsive to initial therapy or their tumors acquire resistance. This results in five-year survival rates of below 25%. New strategies that either kill drug-resistant melanoma cells or prevent their emergence would be extremely valuable. Melanoma, like other cancers, has long been described as being under increased oxidative stress, resulting in an increased reliance on antioxidant defense systems. Changes in redox homeostasis are most apparent during metastasis and during the metabolic reprogramming associated with the development of treatment resistance. This review discusses oxidative stress in melanoma, with a particular focus on targeting antioxidant pathways to limit the emergence of drug resistant cells.

摘要

黑色素瘤是最致命的皮肤癌形式,全球每年约有 60,000 人因此失去生命。尽管已经开发了针对治疗的方法,包括针对仅在癌细胞中表达的突变致癌蛋白的选择性化合物,但许多患者要么对初始治疗无反应,要么其肿瘤产生了耐药性。这导致五年生存率低于 25%。能够杀死耐药性黑色素瘤细胞或防止其出现的新策略将具有极高的价值。黑色素瘤与其他癌症一样,长期以来一直被描述为处于增加的氧化应激下,这导致对抗氧化防御系统的依赖性增加。氧化还原平衡的变化在转移过程中和与治疗耐药性发展相关的代谢重编程过程中最为明显。本文讨论了黑色素瘤中的氧化应激,特别关注靶向抗氧化途径以限制耐药细胞的出现。

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