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Rationale for the treatment of cancer with sodium selenite.

机译:亚硒酸钠治疗癌症的基本原理。

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Epidemiological studies conducted during several decades of the last century have demonstrated the importance of sufficient nutritional supply of selenium (Se) for human health. More importantly, low blood Se levels were found to be associated with an increased incidence and mortality from various types of cancers. Recently, attention of researchers was drawn to the relationship between free radical generation, known otherwise as oxidative stress, and carcinogenesis. It was therefore thought that antioxidants should be beneficial for prevention and inhibition of different malignancies. However, there appeared to be a paradox, because tumor growth is associated with tissue hypoxia that is accompanied by the formation of reductive rather than oxidative free radicals. Various organic and inorganic Se compounds, generally considered to be antioxidants, produced mixed results when tested in animal models and human subjects. Amongst them, sodium selenite has been shown to be the most effective in an in vitroand in vivo carcinogenesis studies. As recently demonstrated, selenite is not an antioxidant, but possesses oxidizing properties in the presence of specific substrates. Thus selenite is capable of oxidizing polythiols to corresponding disulfides, but does not react with monothiols. Such polythiols associated with cancer membrane-bound proteins appear under the reducing conditions of hypoxic tumor tissue. These thiol groups can, in turn, initiate a disulfide exchange reaction with plasma proteins, predominantly with fibrinogen, to form an insoluble and protease-resistant fibrin-like polymer. As the result, tumor cells become surrounded by a coat which masks specific tumor antigens thus allowing cancer cells to escape immune recognition and elimination by natural killer (NK) cells. Selenite by virtue of oxidizing cell membrane thiols, can prevent the formation of the coat and consequently makes cancer cells vulnerable to the immune surveillance and destruction. In addition, selenite may directly activate NK cells, as well as inhibit angiogenesis without undesirable decrease in the oxidative potential of cellular environment. It is, therefore, postulated that sodium selenite, in view of its relative low toxicity, might become a drug of choice for many types of cancer including leukemia.
机译:上个世纪几十年进行的流行病学研究表明,硒的营养供应对人体健康至关重要。更重要的是,发现血液中低硒水平与各种癌症的发病率和死亡率增加有关。最近,引起研究人员注意的是自由基的产生与致癌作用之间的关系,自由基的产生被称为氧化应激。因此,认为抗氧化剂应有益于预防和抑制不同的恶性肿瘤。然而,似乎存在悖论,因为肿瘤生长与组织缺氧有关,组织缺氧伴随着还原性而不是氧化性自由基的形成。在动物模型和人类受试者中进行测试时,通常被认为是抗氧化剂的各种有机和无机硒化合物产生了混合结果。其中,在体外和体内致癌研究中,亚硒酸钠已被证明是最有效的。如最近所证明的,亚硒酸盐不是抗氧化剂,但是在特定底物存在下具有氧化性质。因此,亚硒酸盐能够将多硫醇氧化成相应的二硫化物,但不与单硫醇反应。这种与癌膜结合蛋白相关的多硫醇在低氧肿瘤组织的还原条件下出现。这些硫醇基团继而可以引发与血浆蛋白(主要是与纤维蛋白原)的二硫键交换反应,形成不溶且耐蛋白酶的血纤蛋白样聚合物。结果,肿瘤细胞被一层覆盖特定肿瘤抗原的涂层包围,从而使癌细胞逃避了免疫识别并被自然杀伤(NK)细胞消除。亚硒酸盐凭借氧化细胞膜硫醇的作用,可以防止涂层形成,因此使癌细胞容易受到免疫监视和破坏。另外,亚硒酸盐可以直接活化NK细胞,并抑制血管生成,而不会不希望地降低细胞环境的氧化电位。因此,假定亚硒酸钠鉴于其相对较低的毒性,可能会成为包括白血病在内的许多类型癌症的首选药物。

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