During oncogenesis, cells acquire multiple genetic alterations that confer essential tumor-specific traits, including immortalization, escape from antimitogenic signaling, neovascularization, invasiveness, and metastatic potential. In most instances, these alterations are thought to arise incrementally over years, if not decades. However, recent progress in sequencing cancer genomes has begun to challenge this paradigm, because a radically different phenomenon, termed chromothripsis, has been suggested to cause complex intra- and interchromosomal rearrangements on short timescales. In this Review, we review established pathways crucial for genome integrity and discuss how their dysfunction could precipitate widespread chromosome breakage an...
International audienceThe recent discovery of a new kind of massive chromosomal rearrangement, bapti...
Chromothripsis defines a genetic phenomenon where up to hundreds of clustered chromosomal rearrangem...
Chromothripsis represents a novel phenomenon in the structural variation landscape of cancer genomes...
During oncogenesis, cells acquire multiple genetic alterations that confer essential tumor-specific ...
Genomic alterations that lead to oncogene activation and tumour suppressor loss are important drivin...
Cancer is driven by somatically acquired point mutations and chromosomal rearrangements, conventiona...
Cancer is driven by somatically acquired point mutations and chromosomal rearrangements, conventiona...
Cancer genome sequencing has identified chromothripsis, a complex class of structural genomic rearra...
SummaryCancer is driven by somatically acquired point mutations and chromosomal rearrangements, conv...
Human genomes are continuously subjected to mutations, which can drive genetic diseases and cancer. ...
Abstract Background During the last decade, genome sequencing projects in cancer genomes as well as ...
In recent years, enormous progress has been made with respect to the identification of somatic mutat...
Chromoanagenesis is a catch-all term of recently described catastrophic events that generate complex...
Analysis of whole-genome sequencing data across 2,658 tumors spanning 38 cancer types shows that chr...
The chromothripsis hypothesis suggests an extraordinary one-step catastrophic genomic event allowing...
International audienceThe recent discovery of a new kind of massive chromosomal rearrangement, bapti...
Chromothripsis defines a genetic phenomenon where up to hundreds of clustered chromosomal rearrangem...
Chromothripsis represents a novel phenomenon in the structural variation landscape of cancer genomes...
During oncogenesis, cells acquire multiple genetic alterations that confer essential tumor-specific ...
Genomic alterations that lead to oncogene activation and tumour suppressor loss are important drivin...
Cancer is driven by somatically acquired point mutations and chromosomal rearrangements, conventiona...
Cancer is driven by somatically acquired point mutations and chromosomal rearrangements, conventiona...
Cancer genome sequencing has identified chromothripsis, a complex class of structural genomic rearra...
SummaryCancer is driven by somatically acquired point mutations and chromosomal rearrangements, conv...
Human genomes are continuously subjected to mutations, which can drive genetic diseases and cancer. ...
Abstract Background During the last decade, genome sequencing projects in cancer genomes as well as ...
In recent years, enormous progress has been made with respect to the identification of somatic mutat...
Chromoanagenesis is a catch-all term of recently described catastrophic events that generate complex...
Analysis of whole-genome sequencing data across 2,658 tumors spanning 38 cancer types shows that chr...
The chromothripsis hypothesis suggests an extraordinary one-step catastrophic genomic event allowing...
International audienceThe recent discovery of a new kind of massive chromosomal rearrangement, bapti...
Chromothripsis defines a genetic phenomenon where up to hundreds of clustered chromosomal rearrangem...
Chromothripsis represents a novel phenomenon in the structural variation landscape of cancer genomes...