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6-(7-硝基-2,1,3-苯并恶二唑-4-基硫代)己醇:一种有前途的新型抗癌化合物。

6-(7-nitro-2,1,3-benzoxadiazol-4-ylthio) hexanol: a promising new anticancer compound.

机构信息

The Fourth Clinical School of Nanjing Medical University and Nanjing Medical University Affiliated Cancer Hospital, Baiziting42, Nanjing 210009, China.

The First Clinical School of Nanjing Medical Universityand Department of Orthopedics, the First Affiliated Hospital of Nanjing Medical University, Guangzhou Road300, Nanjing 210009, China.

出版信息

Biosci Rep. 2018 Feb 13;38(1). doi: 10.1042/BSR20171440. Print 2018 Feb 28.

Abstract

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.

摘要

7-硝基-2,1,3-苯并恶二唑(NBD)衍生物是一系列含有 NBD 支架的化合物,不是谷胱甘肽(GSH)肽模拟物,可强烈抑制谷胱甘肽 S-转移酶(GSTs)。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突出的抗癌活性。特别是,6-(7-硝基-2,1,3-苯并恶二唑-4-基硫代)己醇(NBDHEX)得到了广泛研究,它是 GSTP1-1 的非常有效的抑制剂。它在几种肿瘤细胞系中引发细胞凋亡,这种细胞毒性活性在微摩尔和亚微摩尔浓度下观察到。重要的是,研究表明,NBDHEX 通过抑制 GSTs 的催化活性作为抗癌药物发挥作用,避免了抑制剂被特定泵从细胞中排出的不便,并破坏了 GSTP1-1 与关键信号效应物之间的相互作用。此外,一些研究人员还发现 NBDHEX 可以作为晚期自噬抑制剂,这为充分发挥其治疗潜力开辟了新的机会。在这篇综述中,我们总结了该化合物的优势、抗癌机制和类似物,为今后在临床应用中使用 NBDHEX 奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91c3/5809612/f0b367269889/bsr-38-bsr20171440-g1.jpg

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