Suppr超能文献

铟(III)与拉帕醌的配合物:对人乳腺癌细胞的细胞毒性作用及与 DNA 的相互作用。

Indium(III) complexes with lapachol: cytotoxic effects against human breast tumor cells and interactions with DNA.

机构信息

Departamento de Química, Universidade Federal de Minas Gerais, 31.270-901, Belo Horizonte, Minas Gerais, Brazil.

Departamento de Fisiologia e Biofísica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, 31.270-901, Belo Horizonte, Minas Gerais, Brazil.

出版信息

J Biol Inorg Chem. 2024 Aug;29(5):519-529. doi: 10.1007/s00775-024-02062-0. Epub 2024 Jul 16.

Abstract

Lapachol (2-hydroxy-3-(3-methylbut-2-en-1-yl)naphthalene-1,4-dione) is a 1,4-naphthoquinone-derived natural product that presents numerous bioactivities and was shown to have cytotoxic effects against several human tumor cells. Indium(III) complexes with a variety of ligands also exhibit antineoplastic activity. Indium(III) complexes [In(lap)Cl].4HO (1), [In(lap)Cl(EtN)] (2), [In(lap)]·2HO (3) [In(lap)(bipy)Cl] bipy = 2,2'-bipyridine (4) and [In(lap)(phen)Cl] phen = 1,10-phenanthroline (5) were obtained with 2-hydroxy-3-(3-methylbut-2-en-1-yl)naphthalene-1,4-dione (lapachol). Crystal structure determinations for (4) and (5) revealed that the indium(III) center is coordinated to two O atoms from lapachol, two N atoms from 1,10-phenanthroline or 2,2'-bipyridine, and two chloride anions, in a distorted octahedral geometry. Although both complexes (4) and (5) interacted with CT-DNA in vitro by an intercalative mode, only 5 exhibited cytotoxicity against MCF-7 and MDA-MB breast tumor cells. 1,10-phenanthroline and complex (5) presented cytotoxic effects against MCF-7 and MDA-MB cells, with complex (5) being threefold more active than 1,10-phenanthroline on MCF-7 cells. In addition, complex (5) significantly reduced the formation of MDA-MB-231 colonies in a clonogenicity assay. The foregoing results suggest that further studies on the cytotoxic effects and cellular targets of complex (5) are of utmost relevance.

摘要

拉帕醇(2-羟基-3-(3-甲基-2-丁烯-1-基)萘-1,4-二酮)是一种 1,4-萘醌衍生的天然产物,具有多种生物活性,已被证明对多种人类肿瘤细胞具有细胞毒性作用。铟(III)与各种配体形成的配合物也具有抗肿瘤活性。合成了五种铟(III)配合物[In(lap)Cl].4HO(1)、[In(lap)Cl(EtN)](2)、[In(lap)]·2HO(3)、[In(lap)(bipy)Cl]bipy=2,2'-联吡啶(4)和[In(lap)(phen)Cl]phen=1,10-菲啰啉(5),其中 lapachol 为 2-羟基-3-(3-甲基-2-丁烯-1-基)萘-1,4-二酮。配合物(4)和(5)的晶体结构测定表明,铟(III)中心与来自拉帕醇的两个 O 原子、来自 1,10-菲啰啉或 2,2'-联吡啶的两个 N 原子以及两个氯离子配位,形成扭曲的八面体几何形状。尽管配合物(4)和(5)都能在体外通过嵌入模式与 CT-DNA 相互作用,但只有 5 对 MCF-7 和 MDA-MB 乳腺癌肿瘤细胞具有细胞毒性。1,10-菲啰啉和配合物(5)对 MCF-7 和 MDA-MB 细胞均具有细胞毒性作用,配合物(5)对 MCF-7 细胞的活性比 1,10-菲啰啉高三倍。此外,配合物(5)在集落形成实验中显著降低了 MDA-MB-231 集落的形成。上述结果表明,进一步研究配合物(5)的细胞毒性作用和细胞靶标至关重要。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验