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40 Years of Research on Polybrominated Diphenyl Ethers (PBDEs)—A Historical Overview and Newest Data of a Promising Anticancer Drug

机译:40年关于多溴二苯醚(PBDES)-A历史概述和最新数据的历史概览和最新的抗癌药物

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摘要

Polybrominated diphenyl ethers (PBDEs) are a group of molecules with an ambiguous background in literature. PBDEs were first isolated from marine sponges of Dysidea species in 1981 and have been under continuous research to the present day. This article summarizes the two research aspects, (i) the marine compound chemistry research dealing with naturally produced PBDEs and (ii) the environmental toxicology research dealing with synthetically-produced brominated flame-retardant PBDEs. The different bioactivity patterns are set in relation to the structural similarities and dissimilarities between both groups. In addition, this article gives a first structure–activity relationship analysis comparing both groups of PBDEs. Moreover, we provide novel data of a promising anticancer therapeutic PBDE (i.e., 4,5,6-tribromo-2-(2′,4′-dibromophenoxy)phenol; termed P01F08). It has been known since 1995 that P01F08 exhibits anticancer activity, but the detailed mechanism remains poorly understood. Only recently, Mayer and colleagues identified a therapeutic window for P01F08, specifically targeting primary malignant cells in a low µM range. To elucidate the mechanistic pathway of cell death induction, we verified and compared its cytotoxicity and apoptosis induction capacity in Ramos and Jurkat lymphoma cells. Moreover, using Jurkat cells overexpressing antiapoptotic Bcl-2, we were able to show that P01F08 induces apoptosis mainly through the intrinsic mitochondrial pathway.
机译:多溴二苯醚(PBDES)是一组分子,文献中具有含糊不清的背景。 PBDE在1981年首次从呼吸困难物种的海洋海绵中分离出来,并在持续研究目前。本文总结了两项研究方面,(i)海洋复合化学研究处理自然产生的PBDES和(ii)对综合生产的溴化阻燃性PBDE的环境毒理学研究。不同的生物活性模式与两个组之间的结构相似性和异化相比设定。此外,本文提供了第一组PBDE组的第一种结构 - 活动关系分析。此外,我们提供了有前途的抗癌治疗PBDE的新数据(即,4,5,6-三溴-2-(2',4'-二溴苯氧基氧基)苯酚;称为P01F08)。自1995年以来已知,P01F08展示抗癌活动,但详细机制仍然明确。仅近来,Mayer和同事鉴定了P01F08的治疗窗口,特别是在低μm范围内靶向主要恶性细胞。为了阐明细胞死亡诱导的机械途径,我们验证并比较了Ramos和Jurkat淋巴瘤细胞中的细胞毒性和凋亡诱导能力。此外,使用过表达抗曝光Bcl-2的Jurkat细胞,我们能够显示P01F08主要通过内在的线粒体途径诱导细胞凋亡。

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