| Literature DB >> 25065894 |
Adam J Wolpaw1, Brent R Stockwell2.
Abstract
Numerous morphological variations of cell death have been described. These processes depend on a complex and overlapping cellular signaling network, making molecular definition of the pathways challenging. This review describes one solution to this problem for small-molecule-induced death, the creation of high-dimensionality profiles for compounds that can be used to define and compare pathways. Such profiles have been assembled from gene expression measurements, protein quantification, chemical-genetic interactions, chemical combination interactions, cancer cell line sensitivity profiling, quantitative imaging, and modulatory profiling. We discuss the advantages and limitations of these techniques in the study of cell death.Entities:
Keywords: Apoptosis; Cell death; Chemical biology; Gene expression; Nonapoptotic cell death; Profiling; Small molecules
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Year: 2014 PMID: 25065894 DOI: 10.1016/B978-0-12-801430-1.00011-1
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600