Krakowiak Agnieszka, Pietrasik Sylwia
Department of Bioorganic Chemistry, Centre of Molecular and Macromolecular Studies Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland.
Biology (Basel). 2023 Jun 17;12(6):875. doi: 10.3390/biology12060875.
Redox balance is important for the homeostasis of normal cells, but also for the proliferation, progression, and survival of cancer cells. Both oxidative and reductive stress can be harmful to cells. In contrast to oxidative stress, reductive stress and the therapeutic opportunities underlying the mechanisms of reductive stress in cancer, as well as how cancer cells respond to reductive stress, have received little attention and are not as well characterized. Therefore, there is recent interest in understanding how selective induction of reductive stress may influence therapeutic treatment and disease progression in cancer. There is also the question of how cancer cells respond to reductive stress. Selenium compounds have been shown to have chemotherapeutic effects against cancer, and their anticancer mechanism is thought to be related to the formation of their metabolites, including hydrogen selenide (HSe), which is a highly reactive and reducing molecule. Here, we highlight recent reports on the molecular mechanism of how cells recognize and respond to oxidative and reductive stress (1) and the mechanisms through which different types of selenium compounds can generate HSe (2) and thus selectively affect reductive stress under controlled conditions, which may be important for their anticancer effects.
氧化还原平衡对于正常细胞的稳态很重要,对于癌细胞的增殖、进展和存活也很重要。氧化应激和还原应激都可能对细胞有害。与氧化应激相反,还原应激以及癌症中还原应激机制背后的治疗机会,以及癌细胞如何应对还原应激,很少受到关注,也没有得到很好的表征。因此,最近人们对了解选择性诱导还原应激如何影响癌症的治疗和疾病进展很感兴趣。还有一个问题是癌细胞如何应对还原应激。硒化合物已被证明对癌症有化疗作用,其抗癌机制被认为与其代谢产物的形成有关,包括硒化氢(HSe),它是一种高反应性和还原性的分子。在这里,我们重点介绍了最近关于细胞如何识别和应对氧化应激和还原应激的分子机制的报道(1),以及不同类型的硒化合物如何产生HSe的机制(2),从而在可控条件下选择性地影响还原应激,这可能对它们的抗癌作用很重要。