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新型金卡宾配合物有望成为乳腺癌治疗中的多靶点药物。

Novel Au Carbene Complexes as Promising Multi-Target Agents in Breast Cancer Treatment.

作者信息

Ceramella Jessica, Mariconda Annaluisa, Sirignano Marco, Iacopetta Domenico, Rosano Camillo, Catalano Alessia, Saturnino Carmela, Sinicropi Maria Stefania, Longo Pasquale

机构信息

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

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

出版信息

Pharmaceuticals (Basel). 2022 Apr 21;15(5):507. doi: 10.3390/ph15050507.

Abstract

Over the past decade, metal complexes based on -heterocyclic carbenes (NHCs) have attracted great attention due to their wide and exciting applications in material sciences and medicinal chemistry. In particular, the gold-based complexes are the focus of research efforts for the development of new anticancer compounds. Literature data and recent results, obtained by our research group, reported the design, the synthesis and the good anticancer activity of some silver and gold complexes with NHC ligands. In particular, some of these complexes were active towards some breast cancer cell lines. Considering this evidence, here we report some new Au-NHC complexes prepared in order to improve solubility and biological activity. Among them, the compounds and showed an interesting anticancer activity towards the breast cancer MDA-MB-231 and MCF-7 cell lines, respectively. In addition, in vitro and in silico studies demonstrated that they were able to inhibit the activity of the human topoisomerases I and II and the actin polymerization reaction. Moreover, a downregulation of vimentin expression and a reduced translocation of NF-kB into the nucleus was observed. The interference with these vital cell structures induced breast cancer cells' death by triggering the extrinsic apoptotic pathway.

摘要

在过去十年中,基于氮杂环卡宾(NHCs)的金属配合物因其在材料科学和药物化学中的广泛且令人兴奋的应用而备受关注。特别是,金基配合物是开发新型抗癌化合物研究工作的重点。文献数据以及我们研究小组最近获得的结果报道了一些含NHC配体的银和金配合物的设计、合成及其良好的抗癌活性。尤其是,其中一些配合物对某些乳腺癌细胞系具有活性。基于这一证据,在此我们报道了一些为提高溶解性和生物活性而制备的新型金-NHC配合物。其中,化合物 和 分别对乳腺癌MDA-MB-231和MCF-7细胞系表现出有趣的抗癌活性。此外,体外和计算机模拟研究表明,它们能够抑制人类拓扑异构酶I和II的活性以及肌动蛋白聚合反应。此外,观察到波形蛋白表达下调以及NF-κB向细胞核的转位减少。对这些重要细胞结构的干扰通过触发外源性凋亡途径诱导乳腺癌细胞死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09da/9146163/a947a9abafd7/pharmaceuticals-15-00507-g001.jpg

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