Literature DB >> 19833543

Non-genetic cell-to-cell variability and the consequences for pharmacology.

Mario Niepel1, Sabrina L Spencer, Peter K Sorger.   

Abstract

Recent advances in single-cell assays have focused attention on the fact that even members of a genetically identical group of cells or organisms in identical environments can exhibit variability in drug sensitivity, cellular response, and phenotype. Underlying much of this variability is stochasticity in gene expression, which can produce unique proteomes even in genetically identical cells. Here we discuss the consequences of non-genetic cell-to-cell variability in the cellular response to drugs and its potential impact for the treatment of human disease.

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Year:  2009        PMID: 19833543      PMCID: PMC2975492          DOI: 10.1016/j.cbpa.2009.09.015

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  49 in total

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Authors:  Oliver J Rando; Kevin J Verstrepen
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6.  G-protein-coupled receptors function as oligomers in vivo.

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9.  Noise in transcription negative feedback loops: simulation and experimental analysis.

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10.  Stochastic mRNA synthesis in mammalian cells.

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  98 in total

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3.  Quantification and cell-to-cell variation of vascular endothelial growth factor receptors.

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Journal:  Exp Cell Res       Date:  2010-12-23       Impact factor: 3.905

4.  Dissecting genealogy and cell cycle as sources of cell-to-cell variability in MAPK signaling using high-throughput lineage tracking.

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Review 6.  Measuring and modeling apoptosis in single cells.

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Review 7.  Origins of regulated cell-to-cell variability.

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8.  Basal p21 controls population heterogeneity in cycling and quiescent cell cycle states.

Authors:  K Wesley Overton; Sabrina L Spencer; William L Noderer; Tobias Meyer; Clifford L Wang
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9.  Single-cell and subcellular pharmacokinetic imaging allows insight into drug action in vivo.

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10.  Bcl-2 inhibits apoptosis by increasing the time-to-death and intrinsic cell-to-cell variations in the mitochondrial pathway of cell death.

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