Briney Chloe A, Najera Susana, Meier Jordan L
Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD, United States.
Methods Enzymol. 2019;622:431-448. doi: 10.1016/bs.mie.2019.02.037. Epub 2019 Mar 14.
Dysregulated cellular metabolism is an emerging hallmark of cancer. Improved methods to profile aberrant metabolic activity thus have substantial applications as tools for diagnosis and understanding the biology of malignant tumors. Here we describe the utilization of a bioorthogonal ligation to fluorescently detect the TCA cycle oncometabolite fumarate. This method enables the facile measurement of fumarate hydratase activity in cell and tissue samples, and can be used to detect disruptions in metabolism that underlie the genetic cancer syndrome hereditary leiomyomatosis and renal cell cancer (HLRCC). The current method has substantial utility for sensitive fumarate hydratase activity profiling, and also provides a foundation for future applications in diagnostic detection and imaging of cancer metabolism.
细胞代谢失调是癌症新出现的一个特征。因此,改进的异常代谢活性分析方法作为诊断工具和理解恶性肿瘤生物学特性的手段具有重要应用价值。在此,我们描述了利用生物正交连接反应来荧光检测三羧酸循环的致癌代谢物富马酸。该方法能够轻松测量细胞和组织样本中的富马酸水合酶活性,可用于检测导致遗传性平滑肌瘤病和肾细胞癌(HLRCC)这一遗传性癌症综合征的代谢紊乱。当前方法在灵敏的富马酸水合酶活性分析方面具有重要实用价值,也为未来在癌症代谢的诊断检测和成像中的应用奠定了基础。