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利用 SR-FTIR 光谱技术研究肾细胞癌中新型化疗药物的细胞反应。

Investigating cellular responses to novel chemotherapeutics in renal cell carcinoma using SR-FTIR spectroscopy.

机构信息

Manchester Interdisciplinary Biocentre, University of Manchester, UK.

出版信息

Analyst. 2012 Oct 21;137(20):4720-6. doi: 10.1039/c2an35632e.

Abstract

SR-FTIR spectroscopy was evaluated as a technique to discriminate spectral signals of cellular response at the single cell level, when cancer cells are exposed to chemotherapeutics. 5-Fluorouracil, an established drug of known mode of action, was tested against a renal carcinoma cell line (Caki-2), along with two experimental analogues of gold-based compounds. The use of unsupervised principal component analysis (PCA) failed to clearly define any distinction between control and drug treated cell spectra. Supervised principal component linear discriminant analysis (PC-LDA) did have some potential to reveal signatures of cell response and repair but again failed to distinctly discriminate groups of spectra with different drug treatments. Alternatively, clear PCA discrimination was observed in spectra from average cell populations via single point benchtop spectroscopy, probing several cells simultaneously with an increased aperture. The Caki-2 cell line initially appeared to be sensitive to the novel compounds, inducing a cellular response prior to subsequential cell recovery which was assessed by both PCA and cell viability assays.

摘要

SR-FTIR 光谱被评估为一种技术,用于在单个细胞水平上区分细胞对化疗药物的反应的光谱信号。5-氟尿嘧啶是一种作用模式已知的已建立药物,与两种基于金的实验类似物一起对肾癌细胞系(Caki-2)进行了测试。使用无监督主成分分析(PCA)未能清楚地区分对照和药物处理细胞光谱之间的任何区别。监督主成分线性判别分析(PC-LDA)确实有一定的潜力揭示细胞反应和修复的特征,但同样未能清楚地区分具有不同药物处理的光谱组。或者,通过单点台式光谱法观察到来自平均细胞群体的光谱中的清晰 PCA 区分,同时用增加的孔径探测多个细胞。Caki-2 细胞系最初似乎对新型化合物敏感,在随后的细胞恢复之前诱导细胞反应,这通过 PCA 和细胞活力测定来评估。

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