Chromothripsis, DNA repair and checkpoints defects

Semin Cell Dev Biol. 2022 Mar:123:110-114. doi: 10.1016/j.semcdb.2021.02.001. Epub 2021 Feb 13.

Abstract

Chromothripsis is a unique form of genome instability characterized by tens to hundreds of DNA double-strand breaks on one or very few chromosomes, followed by error-prone repair. The derivative chromosome(s) display massive rearrangements, which lead to the loss of tumor suppressor function and to the activation of oncogenes. Chromothripsis plays a major role in cancer as well as in other conditions, such as congenital diseases. In this review, we discuss the repair processes involved in the rejoining of the chromosome fragments, the role of DNA repair and checkpoint defects as a cause for chromothripsis as well as DNA repair defects resulting from chromothripsis. Finally, we consider clinical implications and potential therapeutic vulnerabilities that could be utilized to eliminate tumor cells with chromothripsis.

Keywords: Chromothripsis; Complex genome rearrangements; DNA repair; Genome instability.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Chromothripsis*
  • DNA Breaks, Double-Stranded
  • DNA Repair / genetics
  • Gene Rearrangement
  • Genomic Instability / genetics
  • Humans