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N-杂环卡宾(NHC)银配合物作为针对人体拓扑异构酶和肌动蛋白的多功能化疗药物

N-Heterocyclic Carbene (NHC) Silver Complexes as Versatile Chemotherapeutic Agents Targeting Human Topoisomerases and Actin.

机构信息

Department of Science, University of Basilicata, Viale dell'Ateneo Lucano 10, 85100, Potenza, Italy.

Department of Pharmacy, Health, and Nutritional Sciences, University of Calabria, Via Pietro Bucci, 87036, Arcavacata di, Rende, Italy.

出版信息

ChemMedChem. 2022 Sep 16;17(18):e202200345. doi: 10.1002/cmdc.202200345. Epub 2022 Aug 17.

Abstract

In recent years, the number of people suffering from cancer has risen rapidly and the World Health Organization and U.S. and European governments have identified this pathology as a priority issue. It is known that most bioactive anticancer molecules do not target a single protein but exert pleiotropic effects, simultaneously affecting multiple pathways. In our study, we designed and synthesized a new series of silver N-heterocyclic carbene (NHC) complexes [(NHC) Ag] [AgX ] (X=iodide or acetate). The new complexes were active against two human breast cancer cell lines, MCF-7 and MDA-MB-231. These compounds showed multiple target actions as anticancer, by inhibiting in vitro the activity of the human topoisomerases I and II and interfering with the cytoskeleton dynamic, as also confirmed by in silico studies. Moreover, the antimicrobial activity of these silver complexes was studied against Gram-positive/negative bacteria. These dual properties provide a two-tiered approach, making these compounds of interest to be further deepened for the development of new chemotherapeutic agents.

摘要

近年来,癌症患者的数量迅速增加,世界卫生组织和美国、欧洲政府已将这种病理确定为优先事项。众所周知,大多数具有生物活性的抗癌分子并非针对单一蛋白质,而是发挥多效作用,同时影响多个途径。在我们的研究中,我们设计并合成了一系列新型银氮杂环卡宾(NHC)配合物[(NHC)Ag][AgX](X=碘化物或醋酸盐)。这些新型配合物对两种人乳腺癌细胞系 MCF-7 和 MDA-MB-231 具有活性。这些化合物具有多种抗癌作用,通过体外抑制人拓扑异构酶 I 和 II 的活性并干扰细胞骨架动态,也通过计算机研究得到了证实。此外,还研究了这些银配合物对革兰氏阳性/阴性细菌的抗菌活性。这些双重特性提供了一种双重方法,使这些化合物成为进一步深入开发新化疗药物的关注点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/846c/9804882/defcb1d0a5bb/CMDC-17-0-g006.jpg

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