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癌症中维生素C的转运

Transport of Vitamin C in Cancer.

作者信息

Muñoz-Montesino Carola, Peña Eduardo, Roa Francisco J, Sotomayor Kirsty, Escobar Elizabeth, Rivas Coralia I

机构信息

Departamento de Fisiología and Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.

Departamento de Fisiopatología, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.

出版信息

Antioxid Redox Signal. 2021 Jul;35(1):61-74. doi: 10.1089/ars.2020.8166. Epub 2021 Apr 23.

Abstract

Vitamin C is a powerful antioxidant that has an intricate relationship with cancer and has been studied for more than 60 years. However, the specific mechanisms that allow malignant cells to uptake, metabolize, and compartmentalize vitamin C remain unclear. In normal human cells, two different transporter systems are responsible for its acquisition: glucose transporters (GLUTs) transport the oxidized form of vitamin C (dehydroascorbic acid) and sodium-coupled ascorbic acid transporters (SVCTs) transport the reduced form (ascorbic acid [AA]). In this study, we review the mechanisms described for vitamin C uptake and metabolization in cancer. Several studies performed recently and have provided the scientific community a better understanding of the differential capacities of cancer cells to acquire vitamin C: tumors from different origins do not express SVCTs in the plasma membrane and are only able to acquire vitamin C in its oxidized form. Interestingly, cancer cells differentially express a mitochondrial form of SVCT2. Why tumors have reduced AA uptake capacity at the plasma membrane, but develop the capacity of AA transport within mitochondria, remains a mystery. However, it shows that understanding vitamin C physiology in tumor survival might be key to decipher the controversies in its relationship with cancer. A comprehensive analysis of the mechanisms by which cancer cells acquire, compartmentalize, and use vitamin C will allow the design of new therapeutic approaches in human cancer. 35, 61-74.

摘要

维生素C是一种强大的抗氧化剂,与癌症有着复杂的关系,相关研究已开展60多年。然而,恶性细胞摄取、代谢和分隔维生素C的具体机制仍不清楚。在正常人体细胞中,两种不同的转运系统负责其摄取:葡萄糖转运蛋白(GLUTs)转运维生素C的氧化形式(脱氢抗坏血酸),钠偶联抗坏血酸转运蛋白(SVCTs)转运还原形式(抗坏血酸[AA])。在本研究中,我们综述了癌症中维生素C摄取和代谢的相关机制。最近进行的几项研究使科学界对癌细胞摄取维生素C的不同能力有了更好的理解:不同起源的肿瘤在质膜上不表达SVCTs,只能摄取氧化形式的维生素C。有趣的是,癌细胞差异表达线粒体形式的SVCT2。为什么肿瘤在质膜上的AA摄取能力降低,但却发展出线粒体内AA转运的能力,仍是一个谜。然而,这表明了解维生素C在肿瘤存活中的生理学特性可能是解开其与癌症关系中争议的关键。全面分析癌细胞获取、分隔和利用维生素C的机制将有助于设计针对人类癌症的新治疗方法。35, 61 - 74。

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