Deconstructing stem cell self-renewal: genetic insights into cell-cycle regulation
By K. Orford, D. Scadden. Nature reviews genetics, 2008
915 citations recorded by the source corpus.
Subfields: Cell Biology, Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/7f76d99251096c519ce799c251bcb655aedeed70
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In Cell Biology
In Molecular Biology
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- Suzanne J. Baker
- L. Vallier
- F. Gattazzo
In Oncology
Citations in the corpus
- An embryonic stem cell–like gene expression signature in poorly differentiated aggressive human tumors (2008, background): “As ES cells are characterized by a high proliferation rat”
- Extracellular matrix: A dynamic microenvironment for stem cell niche (2014, background): “maintains stem cells in a quiescent and low metabolic state to prevent stem cell exhaustion [22].”
- Arteriolar niches maintain haematopoietic stem cell quiescence (2013, neutral): “In the bone marrow (BM), recent studies have highlighted the critical influence of the microenvironment in regulating haematopoietic stem cell (HSC) maintenance 4 .”
- Hematopoietic stem cells reversibly switch from dormancy to self-renewal during homeostasis and repair. (2009, positive): “Although it is generally assumed that most immature adult stem cells divide infrequently and are predominantly quiescent (Arai and Suda, 2007; Orford and Scadden, 2008 ), recent reports raise the possibility that dormancy is either not a typical feature of somatic stem cells or that it may depend o”
- Insulin signaling promotes germline proliferation in C. elegans (2010, background): “Although major cell cycle regulators are defined, less is known about the control of cell proliferation by growth factors within developmental contexts (e.g. Edgar and Lehner, 1996; Fichelson et al., 2005; Orford and Scadden, 2008).”
- The autophagy protein Atg7 is essential for hematopoietic stem cell maintenance (2011, background): “Although HSC quiescence has been proposed to play protective functions against stem cell exhaustion and against the acquisition of mutations leading to malignant transformation (Lobo et al., 2007; Orford and Scadden, 2008), the role of autophagy in these processes remains unknown.”
- Senescence impairs successful reprogramming to pluripotent stem cells. (2009, background): “Consequently a short G1 in mouse ES cells allows them to avoid the differentiation-inducing signals mediated by certain mitogenic signalling pathways that are usually active during early G1 in somatic cells (Orford and Scadden, 2008).”
- Hematopoietic stem cell quiescence promotes error prone DNA repair and mutagenesis (2010, background): “In terms of organ maintenance, it is logical to keep long-lived HSCs quiescent in vivo to guard them against DNA replication errors and damage associated with oxidative stress (Rossi et al., 2007; Orford and Scadden, 2008).”
- Prox1 Is Required for Granule Cell Maturation and Intermediate Progenitor Maintenance During Brain Neurogenesis (2010, background): “We do not yet know whether this depletion of NSCs is due to their premature differentiation or their exhaustion resulting from increased proliferation [46].”