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天然产物 Albiziabioside A 与丙酮酸脱氢酶激酶抑制剂二氯乙酸盐偶联诱导细胞凋亡-铁死亡-M2-TAMs 极化用于联合癌症治疗。

Natural Product Albiziabioside A Conjugated with Pyruvate Dehydrogenase Kinase Inhibitor Dichloroacetate To Induce Apoptosis-Ferroptosis-M2-TAMs Polarization for Combined Cancer Therapy.

机构信息

Key Laboratory of Structure-Based Drug Design & Discovery of Ministry of Education , Shenyang Pharmaceutical University , Shenyang 110016 , China.

Institute of Medical Research , Northwestern Polytechnical University , Xi'an 710072 , China.

出版信息

J Med Chem. 2019 Oct 10;62(19):8760-8772. doi: 10.1021/acs.jmedchem.9b00644. Epub 2019 Sep 27.

Abstract

The reprogramming of energy metabolism is considered to be one of the main characteristics of cancer. The development of therapeutic agents targeting glycolysis to alter aberrant glucose metabolism and restore oxidative phosphorylation has emerged as an effective approach for cancer therapy. In this way, we have developed a conjugate AlbA-DCA, which can induce a marked increase in intracellular ROS and alleviate the accumulation of lactic acid in TME. Meanwhile, AlbA-DCA selectively kills cancer cells and exhibits an excellent synergistic effect. Mechanism studies confirm that AlbA-DCA can induce apoptosis and ferroptosis. We also confirm that AlbA-DCA can remold the tumor immunosuppression microenvironment via eliminating M2-TAMs to inhibit both primary and distal tumor progression in a dual-4T1 tumor model in female BALB/c mice. As a result, rational design of natural saponin and PDK inhibitor to induce apoptosis-ferroptosis-M2-TAMs polarization for enhanced cancer therapy is a promising strategy, thus providing a new idea for cancer therapy.

摘要

能量代谢的重编程被认为是癌症的主要特征之一。开发针对糖酵解的治疗药物以改变异常的葡萄糖代谢并恢复氧化磷酸化已成为癌症治疗的有效方法。通过这种方式,我们开发了一种 AlbA-DCA 缀合物,它可以诱导细胞内 ROS 显著增加,并减轻 TME 中乳酸的积累。同时,AlbA-DCA 选择性地杀死癌细胞并表现出优异的协同作用。机制研究证实 AlbA-DCA 可以诱导细胞凋亡和铁死亡。我们还证实 AlbA-DCA 可以通过消除 M2-TAMs 重塑肿瘤免疫抑制微环境,从而抑制雌性 BALB/c 小鼠的双 4T1 肿瘤模型中的原发性和远端肿瘤进展。因此,合理设计天然皂苷和 PDK 抑制剂诱导细胞凋亡-铁死亡-M2-TAMs 极化以增强癌症治疗是一种有前途的策略,从而为癌症治疗提供了新的思路。

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