The impact of clonal diversity and mosaicism on haematopoietic function in Fanconi anaemia

Br J Haematol. 2022 Jan;196(2):274-287. doi: 10.1111/bjh.17653. Epub 2021 Jul 13.

Abstract

Recent advances have facilitated studies of the clonal architecture of the aging haematopoietic system, and provided clues to the mechanisms underlying the origins of hematopoietic malignancy. Much less is known about the clonal composition of haematopoiesis and its impact in bone marrow failure (BMF) disorders, including Fanconi anaemia (FA). Understanding clonality in FA is likely to inform both the marked predisposition to cancer and the rapid erosion of regenerative reserve seen with this disease. This may also hold broader lessons for haematopoietic stem cell biology in other diseases with a clonal restriction. In this review, we focus on the conceptual basis and available tools to study clonality, and highlight insights in somatic mosaicism and malignant evolution in FA in the context of haematopoietic failure and gene therapy.

Keywords: Fanconi anaemia; bone marrow failure; clonal evolution; clonality; gene therapy.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Biomarkers
  • Cell Differentiation / genetics
  • Cell Tracking
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism
  • Clonal Evolution / genetics*
  • Combined Modality Therapy
  • Cytogenetic Analysis
  • DNA Damage
  • Disease Management
  • Disease Susceptibility
  • Fanconi Anemia / diagnosis
  • Fanconi Anemia / etiology*
  • Fanconi Anemia / metabolism*
  • Fanconi Anemia / therapy
  • Gene Expression Regulation
  • Genetic Therapy
  • Genetic Variation*
  • Hematopoiesis / genetics*
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism*
  • Humans
  • Molecular Imaging
  • Mosaicism*
  • Signal Transduction

Substances

  • Biomarkers