发布: 2016年02月05日第6卷第3期 DOI: 10.21769/BioProtoc.1730 浏览次数: 10706
评审: Masahiro MoritaJustine MarsolierAnonymous reviewer(s)
Abstract
An important component of this methodology is to assess the role of the tumor microenvironment on tumor growth and survival. To tackle this problem, we have adapted the original approach of Warburg (Warburg, 1923), by combining thin tissue slices with Stable Isotope Resolved Metabolomics (SIRM) to determine detailed metabolic activity of human tissues. SIRM enables the tracing of metabolic transformations of source molecules such as glucose or glutamine over defined time periods, and is a requirement for detailed pathway tracing and flux analysis. In our approach, we maintain freshly resected tissue slices (both cancerous and non- cancerous from the same organ of the same subject) in cell culture media, and treat with appropriate stable isotope-enriched nutrients, e.g., 13C6-glucose or 13C5, 15N2-glutamine. These slices are viable for at least 24 h, and make it possible to eliminate systemic influence on the target tissue metabolism while maintaining the original 3D cellular architecture. It is therefore an excellent pre-clinical platform for assessing the effect of therapeutic agents on target tissue metabolism and their therapeutic efficacy on individual patients (Xie et al., 2014; Sellers et al., 2015).
Keywords: Tissue slices (组织切片)Materials and Reagents
Equipment
Procedure
文章信息
版权信息
© 2016 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Fan, T. W., Lane, A. N. and Higashi, R. M. (2016). Stable Isotope Resolved Metabolomics Studies in ex vivo TIssue Slices. Bio-protocol 6(3): e1730. DOI: 10.21769/BioProtoc.1730.
分类
癌症生物学 > 细胞能量学 > 肿瘤微环境
癌症生物学 > 细胞能量学 > 动物模型
细胞生物学 > 细胞新陈代谢 > 糖类
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