伊马替尼
脂质体
体内
细胞凋亡
细胞毒性
药理学
医学
体外
毒性
癌症研究
化学
生物
生物化学
生物技术
有机化学
髓系白血病
作者
Rongrong Fu,Rui Chang,A Peng,Changshun Feng,Weifan Zhu,Yi Chen,Tian Xue,Rui Wang,Hui Yan,Dianlong Jia,Jun Li
标识
DOI:10.1080/10837450.2024.2301763
摘要
To solve the problem of resistance of tumor cells to TRAIL and the inevitable side effects of imatinib during treatment, we successfully prepared a kind of multifunctional liposome that encapsulated imatinib in its internal water phase and inserted TRAIL on its membrane in this study, which named ITLPs. The liposomes appeared uniform spherical and the particle size was approximately 150 nm. ITLPs showed high accumulation in TRAIL-resistance cells and HT-29 tumor-bearing mice model. In vitro cytotoxicity assay results showed that the killing activity of HT-29 cells treated with ITLPs increased by 50% and confirmed that this killing activity was mediated by the apoptosis pathway. Through mechanism studies, it was found that ITLPs arrested up to 32.3% of cells in phase M to exert anti-tumor effects. In vivo anti-tumor study showed that ITLPs achieved 61.8% tumor suppression and little toxicity in the HT-29 tumor-bearing mice model. Overall results demonstrated that codelivery of imatinib and TRAIL via liposomes may be a prospective method in the treatment of the TRAIL-resistance tumor.
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