Phospho Flow Cytometry with Fluorescent Cell Barcoding for Single Cell Signaling Analysis and Biomarker Discovery

Aberrant cell signaling plays a central role in cancer development and progression. Most novel targeted therapies are indeed directed at proteins and protein functions, and cell signaling aberrations may therefore serve as biomarkers to indicate personalized treatment options. As opposed to DNA and...

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Bibliographic Details
Published in:Journal of visualized experiments 2018-10 (140)
Main Author: Skånland, Sigrid S
Format: Article
Language:English
Subjects:
Biomarkers - analysis
Biomarkers - metabolism
Cancer Research
Flow Cytometry
Fluorescent Dyes - chemistry
Humans
Leukocytes, Mononuclear - cytology
Leukocytes, Mononuclear - metabolism
Phosphoproteins - analysis
Phosphoproteins - metabolism
Phosphorylation
Signal Transduction
Single-Cell Analysis - methods
Tumor Cells, Cultured
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Summary:Aberrant cell signaling plays a central role in cancer development and progression. Most novel targeted therapies are indeed directed at proteins and protein functions, and cell signaling aberrations may therefore serve as biomarkers to indicate personalized treatment options. As opposed to DNA and RNA analyses, changes in protein activity can more efficiently evaluate the mechanisms underlying drug sensitivity and resistance. Phospho flow cytometry is a powerful technique that measures protein phosphorylation events at the cellular level, an important feature that distinguishes this method from other antibody-based approaches. The method allows for simultaneous analysis of multiple signaling proteins. In combination with fluorescent cell barcoding, larger medium- to high-throughput data-sets can be acquired by standard cytometer hardware in short time. Phospho flow cytometry has applications both in studies of basic biology and in clinical research, including signaling analysis, biomarker discovery and assessment of pharmacodynamics. Here, a detailed experimental protocol is provided for phospho flow analysis of purified peripheral blood mononuclear cells, using chronic lymphocytic leukemia cells as an example.
ISSN:1940-087X
1940-087X
DOI:10.3791/58386