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CNOB/ChrR6 a new prodrug enzyme cancer chemotherapy

机译:CNOB / ChrR6一种新的前药酶癌化学疗法

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摘要

We report the discovery of a new prodrug, 6-chloro-9-nitro-5-oxo-5Hbenzo[a]phenoxazine (CNOB). This prodrug is efficiently activated by ChrR6, the highly active prodrug activating bacterial enzyme we have previously developed. The CNOB/ChrR6 therapy was effective in killing several cancer cell lines in vitro. It also efficiently treated tumors in mice with up to 40% complete remission. 9-amino-6-chloro-5H-benzo[a]phenoxazine-5-one (MCHB) was the only product of CNOB reduction by ChrR6. MCHB binds DNA; at non-lethal concentration, it causes cell accumulation in the S-phase; and at lethal dose it induces cell surface annexinV and caspase 3 and 9 activities. Further, MCHB co-localizes with mitochondria and disrupts their electrochemical potential. Thus, killing by CNOB involves MCHB, which likely induces apoptosis through the mitochondrial pathway. An attractive feature of the CNOB/ChrR6 regime is that its toxic product, MCHB, is fluorescent. This feature proved helpful in in vitro studies, as simple fluorescence measurements provided information on the kinetics of CNOB activation within the cells; MCHB killing mechanism; its generally efficient bystander effect in cells and cell spheroids; and its biodistribution. The emission wavelength of MCHB also permitted its visualization in live animals, allowing noninvasive qualitative imaging of MCHB in mice and the tumor microenvironment. This feature may simplify exploration of barriers to the penetration of MCHB in tumors and their amelioration.
机译:我们报告发现了一种新的前药,6-氯-9-硝基-5-氧代-5H苯并[a]吩恶嗪(CNOB)。该前药被ChrR6有效地激活,ChrR6是我们先前开发的高活性前药激活细菌酶。 CNOB / ChrR6治疗可有效杀死体外的几种癌细胞系。它还可以有效地治疗小鼠肿瘤,完全缓解率高达40%。 9-氨基-6-氯-5H-苯并[a]吩恶嗪-5-酮(MCHB)是ChrR6还原CNOB的唯一产物。 MCHB结合DNA;在非致死浓度下,它会导致细胞在S期积累。并以致死剂量诱导细胞表面膜联蛋白V和caspase 3和9的活性。此外,MCHB与线粒体共定位并破坏其电化学电势。因此,CNOB的杀伤涉及MCHB,它可能通过线粒体途径诱导凋亡。 CNOB / ChrR6方案的一个吸引人的特征是其有毒产物MCHB具有荧光。该功能在体外研究中被证明是有用的,因为简单的荧光测量提供了有关细胞内CNOB活化动力学的信息。 MCHB杀伤机制;在细胞和细胞球体中普遍有效的旁观者效应;及其生物分布。 MCHB的发射波长还允许在活体动物中对其进行可视化,从而可以在小鼠和肿瘤微环境中对MCHB进行无创定性成像。该特征可以简化对MCHB在肿瘤中的渗透和改善的障碍的探索。

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