Why is an energy metabolic defect the common outcome in BMFS?

Paolo Degan, Silvia Ravera, Enrico Cappelli

Research output: Contribution to journalArticle

Abstract

Inherited bone marrow failure syndromes (BMFS) are rare, distressing, inherited blood disorders of children. Although the genetic origin of these pathologies involves genes with different functions, all are associated with progressive haematopoietic impairment and an excessive risk of malignancies. Defects in energy metabolism induce oxidative stress, impaired energy production and an unbalanced ratio between ATP and AMP. This assumes an important role in self-renewal and differentiation in haematopoietic stem cells (HSC) and can play an important role in bone marrow failure. Defects in energetic/respiratory metabolism, in particular in FA and SDS cells, have been described recently and seem to be a pertinent argument in the discussion of the haematopoietic defect in BMFS, as an alternative to the hypotheses already established on this subject, which may shed new light on the evolution of these diseases.

Original languageEnglish
Pages (from-to)1-5
Number of pages5
JournalCell Cycle
DOIs
Publication statusAccepted/In press - Aug 27 2016

Fingerprint

Adenosine Monophosphate
Hematopoietic Stem Cells
Energy Metabolism
Oxidative Stress
Adenosine Triphosphate
Bone Marrow
Pathology
Genes
Neoplasms
Bone Marrow failure syndromes

Keywords

  • Bone marrow failures
  • cancer prone diseases
  • energy metabolism
  • hematopoietic stem cells
  • oxidative stress

ASJC Scopus subject areas

  • Medicine(all)
  • Molecular Biology
  • Developmental Biology
  • Cell Biology

Cite this

Why is an energy metabolic defect the common outcome in BMFS? / Degan, Paolo; Ravera, Silvia; Cappelli, Enrico.

In: Cell Cycle, 27.08.2016, p. 1-5.

Research output: Contribution to journalArticle

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