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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:新型抗癌药物Coti-2用治疗剂协同增量,不会诱导人癌细胞系中的抗性或表现出交叉抗性

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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:新出现的耐药性和药物相关毒性是限制成功癌症治疗的两个主要因素。在临床中使用化学治疗药物的组合,以改善患者结果。然而,癌细胞可以单独或组合获得对药物的抵抗力。抗性肿瘤也可以表现出对其他化学治疗剂的交叉抗性,导致次优化治疗和/或治疗失败。因此,开发诱导没有或几乎没有获得的抗性和有利安全性曲线的新型肿瘤药物是必不可少的。在这里,在这里展示Coti-2,一种新型临床阶段剂,具有多种化学治疗和靶向剂,可增强这些药物在体外和体内的活性。重要的是,在体内组合治疗组中没有观察到明显毒性。此外,与测试的化学治疗药物不同,癌细胞并未产生对Coti-2的抵抗力。最后,一些化学抗性肿瘤细胞系仅显示了对Coti-2的轻度交叉抗性,同时对其保持敏感。

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