aPDL1/aMUC1双抗体修饰阿霉素脂质体的构建及抗肿瘤作用研究

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Shouzhen Zhao, Cuiling Xuan, Wenbin Diao, Ran Bai, Fei Wu, Wenjing Yu, Fan Yang, Jingliang Wu, Wei Xu, Guosheng Jiang, Zhiqin Gao* and Haimei Li*, 
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引用次数: 0

摘要

近年来,癌症的主要治疗方法包括化疗、放疗和手术。然而,诸如预后差、高复发率、低存活率和生活质量下降等挑战仍然存在于癌症管理中。最近,免疫疗法已成为治疗肿瘤的一种有效的治疗方法。为此,我们开发了针对粘蛋白1 (MUC1)和程序性细胞死亡配体1 (PD-L1)的抗体,使脂质体功能化,并加入阿霉素(DOX) (DOX- amuc1 /aPDL1-Lip)。该制剂旨在增强其对癌细胞的靶向能力和抗肿瘤活性。DOX-aMUC1/aPDL1-Lip配方在体内和体外均显示出显著的抗肿瘤作用,有效抑制肿瘤细胞生长。利用针对PD-L1和MUC1的抗体修饰脂质体代表了一种新的癌症治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study on the Construction and Anti-Tumor Effect of aPDL1/aMUC1 Double Antibody Modification of Doxorubicin Liposome

In recent years, the primary treatments for cancer have included chemotherapy, radiotherapy, and surgery. However, challenges such as poor prognosis, high recurrence rates, low survival rates, and diminished quality of life persist in cancer management. Recently, immunotherapy has emerged as a potent therapeutic approach for treating tumors. To this end, we developed antibodies for mucin 1 (MUC1) and programmed cell death ligand 1 (PD-L1) to functionalize liposomes and incorporate doxorubicin (DOX) (DOX-aMUC1/aPDL1-Lip). This formulation is designed to enhance its targeting capability and antitumor activity against cancer cells. The DOX-aMUC1/aPDL1-Lip formulation demonstrated significant antitumor effects both in vivo and in vitro, effectively inhibiting tumor cell growth. Utilizing antibodies against PD-L1 and MUC1 to modify liposomes represents a novel strategy for cancer treatment.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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