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酮洛芬和洛索洛芬铂(IV)配合物通过诱导 DNA 损伤、抑制炎症和增强免疫反应显示出抗肿瘤转移活性。

Ketoprofen and Loxoprofen Platinum(IV) Complexes Displaying Antimetastatic Activities by Inducing DNA Damage, Inflammation Suppression, and Enhanced Immune Response.

机构信息

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

Liaocheng High-Tech Biotechnology Co., Limited, Liaocheng 252059, P. R. China.

出版信息

J Med Chem. 2021 Dec 23;64(24):17920-17935. doi: 10.1021/acs.jmedchem.1c01236. Epub 2021 Dec 1.

Abstract

Metastasis is a major contributor of death in cancer patients, and there is an urgent need for effective treatments of metastatic malignancies. Herein, ketoprofen (KP) and loxoprofen (LP) platinum(IV) complexes with antiproliferative and antimetastatic properties were designed and prepared by integrating chemotherapy and immunotherapy targeting cyclooxygenase-2 (COX-2), matrix metalloproteinase-9 (MMP-9), and programmed death ligand 1 (PD-L1), besides DNA. A mono-KP platinum(IV) complex with a cisplatin core is screened out as a candidate possessing potent anti-proliferative and anti-metastasis activities both in vitro and in vivo. It induces serious DNA damage and further leads to high expression of γ-H2AX and p53. Moreover, it promotes apoptosis of tumor cells through mitochondrial apoptotic pathway Bcl-2/Bax/caspase3. Then, COX-2, MMP-9, NLRP3, and caspase1 as pivotal enzymes igniting inflammation and metastasis are obviously inhibited. Notably, it significantly improves immune response through restraining the expression of PD-L1 to increase CD3 and CD8 T infiltrating cells in tumor tissues.

摘要

转移是癌症患者死亡的主要原因,因此迫切需要有效的转移性恶性肿瘤治疗方法。在此,通过整合针对环氧化酶-2(COX-2)、基质金属蛋白酶-9(MMP-9)和程序性死亡配体 1(PD-L1)以及 DNA 的化学疗法和免疫疗法,设计并制备了具有抗增殖和抗转移特性的酮洛芬(KP)和洛索洛芬(LP)铂(IV)配合物。筛选出一种具有顺铂核心的单 KP 铂(IV)配合物作为候选物,具有体外和体内强大的抗增殖和抗转移活性。它诱导严重的 DNA 损伤,并进一步导致γ-H2AX 和 p53 的高表达。此外,它通过线粒体凋亡途径 Bcl-2/Bax/caspase3 促进肿瘤细胞凋亡。然后,明显抑制引发炎症和转移的关键酶 COX-2、MMP-9、NLRP3 和 caspase1。值得注意的是,它通过抑制 PD-L1 的表达来显著改善免疫反应,从而增加肿瘤组织中 CD3 和 CD8 T 浸润细胞。

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