
doi: 10.2217/epi.09.19
pmid: 22122702
The physiological properties of pluripotency in stem cells and the processes of cell specialization are governed by epigenetic mechanisms, as they are inheritable but not dependent on the cell genotype. There is cumulating evidence demonstrating the presence of cells with stem cell properties within tumors, suggesting that these cells are responsible for tumor growth and heterogeneity. As epigenetic control of self-renewal and pluripotency is a hallmark of stem cells, there is increased interest in studying similar epigenetic mechanisms governing these stemness properties in cancer stem cells. Here we will review the evidence supporting a role for epigenetic mechanisms in the induction of cancer stem cells, with an emphasis on the epigenetic regulatory networks involved in the establishment of normal self-renewal and pluripotency, and their potential deregulation in cancer. We will also discuss the data supporting the plasticity of these mechanisms and its potential therapeutic implications.
Pluripotent Stem Cells, Embryonal Carcinoma Stem Cells, DNA Methylation, Embryo, Mammalian, Models, Biological, Chromatin, Epigenesis, Genetic, Histones, Mice, MicroRNAs, Gene Expression Regulation, Animals
Pluripotent Stem Cells, Embryonal Carcinoma Stem Cells, DNA Methylation, Embryo, Mammalian, Models, Biological, Chromatin, Epigenesis, Genetic, Histones, Mice, MicroRNAs, Gene Expression Regulation, Animals
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 19 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
