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PPMP a novel tubulin-depolymerizing agent against esophageal cancer in patient-derived tumor xenografts

机译:PPMP一种新型的微管蛋白解聚剂可抗食管癌患者自体肿瘤异种移植

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摘要

Esophageal cancer is one of the least studied and deadliest cancers worldwide with a poor prognosis due to limited options for treatment. Chemotherapy agents such as the microtubule-targeting compounds are the mainstay of palliation for advanced esophageal cancer treatment. However, the toxicity and side effects of tubulin-binding agents (TBAs) have promoted the development of novel, more potent but less toxic TBAs. Herein, we identified 2-[4-(3,4-dimethoxyphenyl)-3-methyl-1H-pyrazol-5-yl]-5-[(2-methylprop-2-en-1-yl)oxy] phenol (PPMP) as a novel TBA for esophageal cancer treatment. PPMP markedly inhibited tubulin polymerization, and decreased viability and anchorage-independent growth of esophageal cancer cell lines, effects that were accompanied by G2/M arrest and apoptosis. Importantly, we produced patient-derived esophageal cancer xenografts to evaluate the therapeutic effect of PPMP in a setting that best mimics the clinical context in patients with esophageal cancer. Overall, we identified PPMP as a novel microtubule-destabilizing compound and as a new therapeutic agent against esophageal carcinoma.
机译:由于治疗选择有限,食管癌是全世界研究最少,死亡最严重的癌症之一,预后较差。化疗药物,如靶向微管的化合物,是晚期食管癌治疗的主要手段。然而,微管蛋白结合剂(TBA)的毒性和副作用促进了新型,更有效但毒性较小的TBA的发展。在这里,我们确定了2- [4-(3,4-二甲氧基苯基)-3-甲基-1H-吡唑-5-基] -5-[(2-甲基丙-2-烯-1-基)氧基]苯酚( PPMP)作为食管癌治疗的新型TBA。 PPMP显着抑制了微管蛋白的聚合,并降低了食管癌细胞系的活力和不依赖锚定的生长,并伴有G2 / M阻滞和凋亡。重要的是,我们生产了源自患者的食道癌异种移植物,以评估PPMP在最能模拟食道癌患者临床情况的环境中的治疗效果。总体而言,我们将PPMP鉴定为一种新型的微管破坏性化合物和抗食管癌的新型治疗剂。

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