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具有显著抗癌活性的铂(IV)-金(I)制剂:二维和三维三阴性乳腺癌模型中的精选研究

Platinum(IV)-Gold(I) Agents with Promising Anticancer Activity: Selected Studies in 2D and 3D Triple-Negative Breast Cancer Models.

作者信息

López-Hernández Javier E, Nayeem Nazia, Cerón-Carrasco José P, Ahad Afruja, Hafeez Aiman, León Ignacio E, Contel Maria

机构信息

Department of Chemistry and Brooklyn College Cancer Center, Brooklyn College, The City University of New York, Brooklyn, NY, 11210, USA.

Biology, Chemistry and Biochemistry PhD Programs, The Graduate Center, The City University of New York, New York, NY, 10016, USA.

出版信息

Chemistry. 2023 Oct 23;29(59):e202302045. doi: 10.1002/chem.202302045. Epub 2023 Sep 5.

Abstract

New heterometallic binuclear and trinuclear platinum(IV)-gold(I) compounds of the type [Pt(L) Cl (OH){(OOC-4-C H -PPh )AuCl} ] (L=NH , n=2; x=1, 2; L=diaminocyclohexane, DACH, n=1; x=2) are described. These compounds are cytotoxic and selective against a small panel of renal, bladder, ovarian, and breast cancer cell lines. We selected a trinuclear PtAu compound containing the Pt core based on oxaliplatin, to further investigate its cell-death pathway, cell and organelle uptake and anticancer effects against the triple-negative breast cancer (TNBC) MDA-MB-231 cell line. This compound induces apoptosis and accumulates mainly in the nucleus and mitochondria. It also exerts remarkable antimigratory and antiangiogenic properties, and has a potent cytotoxic effect against TNBC 3D spheroids. Trinuclear compounds do not seem to display relevant interactions with calf thymus (CT) DNA and plasmid (pBR322) even in the presence of reducing agents, but inhibit pro-angiogenic enzyme thioredoxin reductase (TrxR) in TNBC cells.

摘要

本文描述了新型的异金属双核和三核铂(IV)-金(I)化合物,其化学式为[Pt(L)Cl(OH){(OOC-4-C₆H₄-PPh₂)AuCl}](L=NH₃,n=2;x=1,2;L=二氨基环己烷,DACH,n=1;x=2)。这些化合物具有细胞毒性,且对一小部分肾、膀胱、卵巢和乳腺癌细胞系具有选择性。我们选择了一种基于奥沙利铂含铂核心的三核铂金化合物,以进一步研究其细胞死亡途径、细胞和细胞器摄取以及对三阴性乳腺癌(TNBC)MDA-MB-231细胞系的抗癌作用。该化合物诱导细胞凋亡,主要积聚在细胞核和线粒体中。它还具有显著的抗迁移和抗血管生成特性,并且对TNBC 3D球体具有强大的细胞毒性作用。即使在存在还原剂的情况下,三核化合物似乎也不会与小牛胸腺(CT)DNA和质粒(pBR322)发生相关相互作用,但会抑制TNBC细胞中的促血管生成酶硫氧还蛋白还原酶(TrxR)。

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