Lipinski Boguslaw
H.S. Research, P.O. Box 1815, Boston, MA 02460, USA.
Med Hypotheses. 2005;64(4):806-10. doi: 10.1016/j.mehy.2004.10.012.
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 vitro and 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.
上世纪几十年间开展的流行病学研究已证明,充足的硒(Se)营养供应对人类健康至关重要。更重要的是,人们发现血液中硒水平低与各类癌症的发病率和死亡率增加有关。最近,研究人员的注意力被吸引到自由基生成(即氧化应激)与致癌作用之间的关系上。因此,人们认为抗氧化剂对预防和抑制不同的恶性肿瘤应该是有益的。然而,似乎存在一个悖论,因为肿瘤生长与组织缺氧相关,而组织缺氧会伴随着还原性而非氧化性自由基的形成。各种有机和无机硒化合物通常被认为是抗氧化剂,但在动物模型和人体试验中测试时,结果不一。其中,亚硒酸钠在体外和体内致癌研究中已显示出是最有效的。正如最近所证明的,亚硒酸盐不是抗氧化剂,而是在特定底物存在时具有氧化特性。因此,亚硒酸盐能够将多硫醇氧化为相应的二硫化物,但不与单硫醇反应。与癌症膜结合蛋白相关的此类多硫醇出现在缺氧肿瘤组织的还原条件下。这些硫醇基团进而可与血浆蛋白,主要是与纤维蛋白原引发二硫键交换反应,形成不溶性且抗蛋白酶的纤维蛋白样聚合物。结果,肿瘤细胞被一层掩盖特定肿瘤抗原的包膜所包围,从而使癌细胞能够逃避自然杀伤(NK)细胞的免疫识别和清除。亚硒酸盐凭借氧化细胞膜硫醇,可防止包膜形成,从而使癌细胞易受免疫监视和破坏。此外,亚硒酸盐可能直接激活NK细胞,以及抑制血管生成,而不会使细胞环境的氧化电位出现不良降低。因此,鉴于其相对较低的毒性,推测亚硒酸钠可能成为包括白血病在内的多种癌症的首选药物。