Self-renewal |
High capacity [27, 28] |
High capacity [10, 64, 70, 71] |
|
Cell cycle duration |
Long. Tissue-regulated generation of transit amplifying progenitors [28] |
Redundant self-renewal pathways become activated. Pathological self-renewal balance over differentiation [72] |
|
Genome repair abilities |
Yes [73, 74] |
Altered (constant generation of new mutations and epigenetic profiles to generate clones with strong adaption capacity to aggressive environments) [46, 73]. Hypoxia mediated cell cycle lengthening and DNA repair [75, 76]. Shorter cell cycle contribution [12] |
|
Microenvironmental protection by niche from noxious agents |
Yes [77] |
Yes [11, 23] |
|
Location at hierarchy |
Basal compartment [27] |
Basal compartment [72] |
|
Transit amplifying compartment |
Progenitor cells have short cycles to generate enough numbers of normal differentiated cells [47, 78] |
It seems to be present as the basis for rapid growth of tumors. Progenitor cells have short cycles [10] |
|
Plasticity |
Can go back and forth between differentiation and dedifferentiation states [79] |
Epithelial mesenchymal transition and self-renewal acquisition [10, 80, 81] Dedifferentiation and mutation accumulation in committed cells [22] |