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6-(7-nitro-213-benzoxadiazol-4-ylthio) hexanol: a promising new anticancer compound

机译:6-(7-硝基-213-苯并恶二唑-4-基硫基)己醇:一种有前途的新型抗癌化合物

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摘要

The 7-nitro-2,1,3-nitrobenzoxadiazole (NBD) derivatives are a series of compounds containing the NBD scaffold that are not glutathione (GSH) peptidomimetics, and result in a strong inhibition of glutathione S-transferases (GSTs). Growing evidences highlight their pivotal roles and outstanding anticancer activity in different tumor models. In particular, 6-(7-nitro-2,1,3-benzoxadiazol-4-ylthio) hexanol (NBDHEX) is extensively studied, which is a very efficient inhibitor of GSTP1-1. It triggers apoptosis in several tumor cell lines and this cytotoxic activity is observed at micro and submicromolar concentrations. Importantly, studies have shown that NBDHEX acts as an anticancer drug by inhibiting GSTs catalytic activity, avoiding inconvenience of the inhibitor extrusion from the cell by specific pumps and disrupting the interaction between the GSTP1-1 and key signaling effectors. Additionally, some researchers also have discovered that NBDHEX can act as late-phase autophagy inhibitor, which opens new opportunities to fully exploit its therapeutic potential. In this review, we summarize the advantages, anticancer mechanisms, and analogs of this compound, which will establish the basis on the usage of NBDHEX in clinical applications in future.
机译:7-硝基-2,1,3-硝基苯并恶二唑(NBD)衍生物是一系列包含NBD支架的化合物,这些化合物不是谷胱甘肽(GSH)拟肽,会强烈抑制谷胱甘肽S-转移酶(GST)。越来越多的证据强调了它们在不同肿瘤模型中的关键作用和出色的抗癌活性。特别地,广泛研究了6-(7-硝基-2,1,3-苯并恶二唑-4-基硫基)己醇(NBDHEX),它是一种非常有效的GSTP1-1抑制剂。它触发了几种肿瘤细胞系的凋亡,并且在微摩尔和亚微摩尔浓度下都观察到了这种细胞毒活性。重要的是,研究表明NBDHEX通过抑制GST的催化活性,避免抑制剂被特异性泵从细胞中挤出,以及破坏GSTP1-1与关键信号传导因子之间的相互作用而充当抗癌药。此外,一些研究人员还发现NBDHEX可以作为晚期自噬抑制剂,这为充分利用其治疗潜力提供了新的机会。在这篇综述中,我们总结了该化合物的优点,抗癌机制和类似物,将为NBDHEX在未来临床应用中的使用奠定基础。

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