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含核氨基酸的Pt(II)配合物的合成、抗增殖活性及DNA结合研究

Synthesis, Antiproliferative Activity, and DNA Binding Studies of Nucleoamino Acid-Containing Pt(II) Complexes.

作者信息

Riccardi Claudia, Capasso Domenica, Coppola Angela, Platella Chiara, Montesarchio Daniela, Di Gaetano Sonia, Roviello Giovanni N, Musumeci Domenica

机构信息

Department of Chemical Sciences, University of Napoli Federico II, 80126 Napoli, Italy.

CESTEV, University of Napoli Federico II, 80145 Napoli, Italy.

出版信息

Pharmaceuticals (Basel). 2020 Sep 30;13(10):284. doi: 10.3390/ph13100284.

Abstract

We here report our studies on the reaction with the platinum(II) ion of a nucleoamino acid constituted by the l-2,3-diaminopropanoic acid linked to the thymine nucleobase through a methylenecarbonyl linker. The obtained new platinum complexes, characterized by spectroscopic and mass spectrometric techniques, were envisaged to exploit synergistic effects due to the presence of both the platinum center and the nucleoamino acid moiety. The latter can be potentially useful to protect the complexes from early deactivation, as well as to facilitate their cell internalization. The biological activity of the complexes in terms of antiproliferative effects was evaluated in vitro on different cancer cell lines and healthy cells, showing the best results on human cervical adenocarcinoma (HeLa) cells along with good selectivity for cancer over normal cells. In contrast, the metal-free nucleoamino acid did not show any cytotoxicity on both normal and cancer cell lines. Finally, the ability of the novel Pt(II) complexes to bind various DNA model systems was investigated by circular dichroism (CD) spectroscopy and polyacrylamide gel electrophoresis analyses proving that the newly obtained compounds can potentially target DNA, similarly to other well-known anticancer Pt complexes, with a peculiar G-quadruplex vs. duplex selectivity.

摘要

我们在此报告了关于一种核氨基酸与铂(II)离子反应的研究,该核氨基酸由通过亚甲基羰基连接基与胸腺嘧啶碱基相连的L-2,3-二氨基丙酸构成。通过光谱和质谱技术对获得的新型铂配合物进行了表征,设想其利用铂中心和核氨基酸部分的存在产生协同效应。后者可能有助于保护配合物免于早期失活,并促进其细胞内化。在不同癌细胞系和健康细胞上体外评估了配合物在抗增殖作用方面的生物活性,结果显示对人宫颈腺癌(HeLa)细胞效果最佳,且对癌细胞比对正常细胞具有良好的选择性。相比之下,无金属的核氨基酸对正常细胞系和癌细胞系均未显示出任何细胞毒性。最后,通过圆二色性(CD)光谱和聚丙烯酰胺凝胶电泳分析研究了新型Pt(II)配合物与各种DNA模型系统结合的能力,证明新获得的化合物与其他著名的抗癌铂配合物类似,可能以一种特殊的G-四链体与双链体选择性靶向DNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfa8/7600948/d0a77b93b778/pharmaceuticals-13-00284-g001.jpg

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