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靶向上皮-间充质转化的 Canadine 铂(IV)配合物作为抗增殖和抗转移剂。

Canadine Platinum(IV) Complexes Targeting Epithelial-Mesenchymal Transition as Antiproliferative and Antimetastatic Agents.

机构信息

Institute of Biopharmaceutical Research, Liaocheng University, Liaocheng 252059, P.R. China.

Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640, China.

出版信息

J Med Chem. 2024 Aug 8;67(15):12868-12886. doi: 10.1021/acs.jmedchem.4c00843. Epub 2024 Jul 28.

Abstract

Epithelial-mesenchymal transition (EMT) is a critical process for cancer progression, which is crucial in inhibiting the immunity in tumors and further boosting tumor metastasis. The suppression of EMT represents a promising strategy for inhibiting metastatic tumors. Herein, a series of new canadine platinum(IV) conjugates with potent antiproliferative and antimetastatic activities were developed, which activated by suppressing EMT and provoking immune response in tumors besides causing DNA injury. The complexes could covalently conjugate to DNA and induce mitochondria-mediated apoptosis via Bcl-2/Bax/caspase3 signaling. The EMT process was remarkably inhibited by suppressing the Wnt/β-catenin pathway, reversing the inflammatory tumor microenvironment, and inhibiting the HIF-1α pathway, which further resulted in the inhibited angiogenesis in tumors. Moreover, the antitumor immunity was elevated by blocking immune checkpoints PD-L1 and CD47 accompanied by the improvement of CD3 and CD8 T lymphocytes and the macrophage polarization from M2- toward M1-type simultaneously in tumors.

摘要

上皮-间充质转化(EMT)是癌症进展的关键过程,它在抑制肿瘤中的免疫逃逸和促进肿瘤转移方面起着至关重要的作用。抑制 EMT 是抑制转移性肿瘤的一种很有前途的策略。在此,开发了一系列具有强效增殖抑制和抗转移活性的新型加拿大碱铂(IV)缀合物,这些化合物通过抑制 EMT 和在肿瘤中引发免疫反应,以及造成 DNA 损伤来发挥作用。这些配合物可以通过 Bcl-2/Bax/caspase3 信号通路与 DNA 共价结合,并诱导线粒体介导的细胞凋亡。EMT 过程通过抑制 Wnt/β-catenin 通路、逆转炎症性肿瘤微环境以及抑制 HIF-1α 通路而被显著抑制,这进一步导致肿瘤中的血管生成受到抑制。此外,通过阻断免疫检查点 PD-L1 和 CD47,同时提高肿瘤中 CD3 和 CD8 T 淋巴细胞以及巨噬细胞从 M2 向 M1 型的极化,提高了抗肿瘤免疫。

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