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Cell cycle inhibitors in normal and tumor stem cells

Journal

ONCOGENE
Volume 23, Issue 43, Pages 7256-7266

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1207945

Keywords

adult stem cell; hematopoietic stem cell; tumor stem cell; tissue regeneration; self-renewal; cell cycle; cyclin-dependent kinase inhibitor; p21; p27; p18; p16; Rb protein

Funding

  1. NHLBI NIH HHS [HL70561] Funding Source: Medline
  2. NIDDK NIH HHS [DK02761] Funding Source: Medline

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Emerging data suggest that stem cells may be one of the key elements in normal tissue regeneration and cancer development, although they are not necessarily the same entity in both scenarios. As extensively demonstrated in the hematopoietic system, stem cell repopulation is hierarchically organized and is intrinsically limited by the intracellular cell cycle inhibitors. Their inhibitory effects appear to be highly associated with the differentiation stage in stem/progenitor pools. While this negative regulation is important for maintaining homeostasis, especially at the stem cell level under physiological cues or pathological insults, it constrains the therapeutic use of adult stem cells in vitro and restricts endogenous tissue repair after injury. On the other hand, disruption of cell cycle inhibition may contribute to the formation of the so-called 'tumor stem cells' (TSCs) that are currently hypothesized to be partially responsible for tumorigenesis and recurrence of cancer after conventional therapies. Therefore, understanding how cell cycle inhibitors control stem cells may offer new strategies not only for therapeutic manipulations of normal stem cells but also for novel therapies selectively targeting TSCs.

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