Jamieson Lauren E, Wetherill Corinna, Faulds Karen, Graham Duncan
Centre for Molecular Nanometrology , WestCHEM , Department of Pure and Applied Chemistry, Technology and Innovation Centre , University of Strathclyde , 99 George Street , Glasgow , G1 1RD , UK . Email:
Chem Sci. 2018 Jul 31;9(34):6935-6943. doi: 10.1039/c8sc02312c. eCollection 2018 Sep 14.
lipid synthesis is upregulated in cancer cells and inhibiting these pathways has displayed anti-tumour activity. Here we use Raman spectroscopy, focusing solely on high wavenumber spectra, to detect changes in lipid composition in single cells in response to drugs targeting lipid synthesis. Unexpectedly, the beta-blocker propranolol showed selectively towards cancerous PC3 compared to non-cancerous PNT2 prostate cells, demonstrating the potential of this approach to identify new anti-cancer drug leads. A unique and simple ratiometric approach for intracellular lipid investigation is reported using statistical analysis to create phenotypic 'barcodes', a globally applicable strategy for Raman drug-cell studies. High wavenumber spectral analysis is compatible with low cost glass substrates, easily translatable into the cytological work stream. The analytical strength of this technique could have a significant impact on cancer treatment through vastly improved understanding of cancer cell metabolism, and thus guide drug design and enhance personalised medicine strategies.
脂质合成在癌细胞中上调,抑制这些途径已显示出抗肿瘤活性。在这里,我们使用拉曼光谱,仅关注高波数光谱,以检测单细胞中脂质组成的变化,以响应靶向脂质合成的药物。出乎意料的是,与非癌性PNT2前列腺细胞相比,β受体阻滞剂普萘洛尔对癌性PC3细胞表现出选择性,证明了这种方法在识别新的抗癌药物先导物方面的潜力。报告了一种独特而简单的用于细胞内脂质研究的比率方法,该方法使用统计分析来创建表型“条形码”,这是一种适用于拉曼药物-细胞研究的全球通用策略。高波数光谱分析与低成本玻璃基板兼容,易于转化为细胞学工作流程。该技术的分析优势可能会通过极大地改善对癌细胞代谢的理解,对癌症治疗产生重大影响,从而指导药物设计并加强个性化医疗策略。