In Vitro and In Vivo Evaluation of Tubulin Inhibitors with Non-Small Cell Lung Cancer Pre-Clinical Models

Rati Lama, Danting Liu, B. Zhong, D. Danielpour, Aimin Zhou, Bin Su
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引用次数: 2

Abstract

Synthetic small molecule tubulin inhibitors have many advantages as novel anti-cancer agents compared to the current tubulin inhibitors generated from natural products. Our previous studies led to the design and synthesis of a series of novel tubulin inhibitors. Some of these compounds also inhibited heat shock protein 27 (Hsp27), and showed promising in vitro anti-cancer activities in several breast cancer cell lines at sub nano-molar concentrations. However, whether these compounds could suppress tumor growth in animals was not investigated yet. In the current study, to identify the best drug candidates, therapeutic efficacy of the representative compounds from previous analyses was evaluated using non-small cell lung cancer preclinical models. These agents dose-dependently inhibited the growth of lung cancer cells in both monolayer cultures and three-dimensional multicellular spheroids. Several compounds also showed promising tumor growth suppressive activity in nude mice xenograft model.
微管蛋白抑制剂在非小细胞肺癌临床前模型中的体外和体内评价
合成小分子微管蛋白抑制剂作为新型抗癌药物,与目前天然产物微管蛋白抑制剂相比具有许多优点。我们之前的研究导致了一系列新型微管蛋白抑制剂的设计和合成。其中一些化合物还能抑制热休克蛋白27 (Hsp27),并在亚纳米摩尔浓度的几种乳腺癌细胞系中显示出良好的体外抗癌活性。然而,这些化合物是否能抑制动物肿瘤的生长还没有研究。在目前的研究中,为了确定最佳的候选药物,使用非小细胞肺癌临床前模型评估了先前分析中具有代表性的化合物的治疗效果。这些药物剂量依赖性地抑制肺癌细胞在单层培养和三维多细胞球体中的生长。几种化合物在裸鼠异种移植瘤模型中也显示出良好的肿瘤生长抑制活性。
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