Department of Sciences and Chemical Technologies, University of Rome "Tor Vergata", Italy.
Amino Acids. 2011 Jun;41(1):103-12. doi: 10.1007/s00726-010-0522-6. Epub 2010 Mar 6.
Natural organosulfur compounds (OSCs) have been shown to have chemopreventive effects and to suppress the proliferation of tumor cells in vitro through the induction of apoptosis. The biochemical mechanisms underlying the antitumorigenic and anti-proliferative effects of garlic-derived OSCs are not fully understood. Several modes of action of these compounds have been proposed, and it seems likely that the rate of clearance of allyl sulfur groups from cells is a determinant of the overall response. The aim of this review is to focus attention on the effects of natural allyl sulfur compounds on the cell detoxification system in normal and tumor cells. It has been already reported that several natural allyl sulfur compounds induce chemopreventive effects by affecting xenobiotic metabolizing enzymes and inducing their down-activation. Moreover, different effects of water- and oil-soluble allyl sulfur compounds on enzymes involved in the detoxification system of rat tissues have been observed. A direct interaction of the garlic allyl sulfur compounds with proteins involved in the detoxification system was studied in order to support the hypothesis that proteins possessing reactive thiol groups and that are involved in the detoxification system and in the cellular redox homeostasis, are likely the preferential targets of these compounds. The biochemical transformation of the OSCs in the cell and their adducts with thiol functional groups of these proteins, could be considered relevant events to uncover the anticancer properties of the allyl sulfur compounds. Although additional studies, using proteomic approaches and transgenic models, are needed to identify the molecular targets and modes of action of these natural compounds, the allyl sulfur compounds can represent potential ideal agents in anticancer therapy, either alone or in association with other antitumor drugs.
天然有机硫化合物 (OSC) 已被证明具有化学预防作用,并通过诱导细胞凋亡来抑制肿瘤细胞的增殖。大蒜衍生的 OSC 抗肿瘤和抗增殖作用的生化机制尚未完全阐明。这些化合物的几种作用模式已经被提出,而且细胞中烯丙基硫基团的清除速度似乎是决定整体反应的一个因素。本综述的目的是关注天然烯丙基硫化合物对正常和肿瘤细胞细胞解毒系统的影响。已经有报道称,几种天然烯丙基硫化合物通过影响外源代谢酶并诱导其失活来发挥化学预防作用。此外,还观察到水溶性和油溶性烯丙基硫化合物对参与大鼠组织解毒系统的酶的不同影响。为了支持这样的假设,即具有反应性巯基基团并参与解毒系统和细胞氧化还原稳态的蛋白质可能是这些化合物的优先靶标,研究了大蒜烯丙基硫化合物与参与解毒系统的蛋白质之间的直接相互作用。可以认为,OSC 在细胞中的生化转化及其与这些蛋白质巯基功能基团的加合物,是揭示烯丙基硫化合物抗癌特性的相关事件。尽管需要使用蛋白质组学方法和转基因模型进行更多的研究来确定这些天然化合物的分子靶标和作用模式,但烯丙基硫化合物可以作为抗癌治疗的潜在理想药物,无论是单独使用还是与其他抗肿瘤药物联合使用。