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体外傅里叶变换红外显微镜分析顺铂和 5-氟尿嘧啶处理的原发性口腔鳞状细胞癌细胞:一种研究药物-细胞相互作用的新光谱方法。

In vitro FTIR microspectroscopy analysis of primary oral squamous carcinoma cells treated with cisplatin and 5-fluorouracil: a new spectroscopic approach for studying the drug-cell interaction.

机构信息

Dipartimento di Scienze della Vita e dell'Ambiente, Università Politecnica delle Marche, via Brecce Bianche, 60131 Ancona, Italy.

出版信息

Analyst. 2018 Jul 9;143(14):3317-3326. doi: 10.1039/c8an00602d.

DOI:10.1039/c8an00602d
PMID:29931010
Abstract

In the present study, human primary oral squamous carcinoma cells treated with cisplatin and 5-fluorouracil were analyzed, for the first time, by in vitro FTIR Microspectroscopy (FTIRM), to improve the knowledge on the biochemical pathways activated by these two chemotherapy drugs. To date, most of the studies regarding FTIRM cellular analysis have been executed on fixed cells from immortalized cell lines. FTIRM analysis performed on primary tumor cells under controlled hydrated conditions provides more reliable information on the biochemical processes occurring in in vivo tumor cells. This spectroscopic analysis allows to get on the same sample and at the same time an overview of the composition and structure of the most remarkable cellular components. In vitro FTIRM analysis of primary oral squamous carcinoma cells evidenced a time-dependent drug-specific cellular response, also including apoptosis triggering. Furthermore, the univariate and multivariate analyses of IR data evidenced meaningful spectroscopic differences ascribable to alterations affecting cellular proteins, lipids and nucleic acids. These findings suggest for the two drugs different pathways and extents of cellular damage, not provided by conventional cell-based assays (MTT assay and image-based cytometry).

摘要

在本研究中,首次通过体外傅里叶变换红外显微镜(FTIRM)分析了经顺铂和 5-氟尿嘧啶处理的人原发性口腔鳞状癌细胞,以增进对这两种化疗药物激活的生化途径的认识。迄今为止,大多数关于 FTIRM 细胞分析的研究都是在固定的永生化细胞系上进行的。在受控水合条件下对原发性肿瘤细胞进行的 FTIRM 分析可提供更可靠的信息,说明发生在体内肿瘤细胞中的生化过程。这种光谱分析可以在同一样品上同时获得最显著的细胞成分的组成和结构的概述。对原发性口腔鳞状癌细胞的体外 FTIRM 分析表明,药物具有时间依赖性的特定细胞反应,包括触发细胞凋亡。此外,IR 数据的单变量和多变量分析表明,由于影响细胞蛋白、脂质和核酸的改变,存在有意义的光谱差异。这些发现表明,这两种药物作用于细胞的途径和程度不同,这无法通过传统的基于细胞的检测(MTT 检测和基于图像的细胞计数)提供。

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