首页> 美国卫生研究院文献>other >Novel anti-cancer drug COTI-2 synergizes with therapeutic agents and does not induce resistance or exhibit cross-resistance in human cancer cell lines
【2h】

Novel anti-cancer drug COTI-2 synergizes with therapeutic agents and does not induce resistance or exhibit cross-resistance in human cancer cell lines

机译:新型抗癌药COTI-2与治疗剂协同作用在人癌细胞系中不诱导耐药性或表现出交叉耐药性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Emerging drug-resistance and drug-associated toxicities are two major factors limiting successful cancer therapy. Combinations of chemotherapeutic drugs have been used in the clinic to improve patient outcome. However, cancer cells can acquire resistance to drugs, alone or in combination. Resistant tumors can also exhibit cross-resistance to other chemotherapeutic agents, resulting in sub-optimal treatment and/or treatment failure. Therefore, developing novel oncology drugs that induce no or little acquired resistance and with a favorable safety profile is essential. We show here that combining COTI-2, a novel clinical stage agent, with multiple chemotherapeutic and targeted agents enhances the activity of these drugs in vitro and in vivo. Importantly, no overt toxicity was observed in the combination treatment groups in vivo. Furthermore, unlike the tested chemotherapeutic drugs, cancer cells did not develop resistance to COTI-2. Finally, some chemo-resistant tumor cell lines only showed mild cross-resistance to COTI-2 while most remained sensitive to it.
机译:新兴的耐药性和药物相关的毒性是限制成功癌症治疗的两个主要因素。临床上已经使用化学治疗药物的组合来改善患者预后。然而,癌细胞可以单独或组合获得对药物的抗性。抗药性肿瘤还可能表现出与其他化学治疗剂的抗药性,导致治疗效果欠佳和/或治疗失败。因此,开发新颖的,不会或几乎不会引起耐药性且具有良好安全性的肿瘤药物至关重要。我们在这里显示将新型临床分期治疗药COTI-2与多种化学治疗药和靶向药结合使用,可增强这些药物在体外和体内的活性。重要的是,在体内联合治疗组中未观察到明显的毒性。此外,与所测试的化疗药物不同,癌细胞对COTI-2没有抵抗力。最后,一些化学耐药的肿瘤细胞系仅对COTI-2表现出轻微的交叉耐药性,而大多数仍对它敏感。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号