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PMID: 21628407 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Chromothripsis identifies a rare and aggressive entity among newly diagnosed multiple myeloma patients.

Blood ·Vol. 118 ·No. 3 ·2011-07-21 ·Pages 675-8

Magrangeas F, Avet-Loiseau H, Munshi NC, Minvielle S

Abstract

Multiple myeloma (MM) develops from a premalignant plasma cell proliferative disorder, and with time can progress to a more aggressive disease in extramedullary locations. The gradually clinical evolution is supported by clonal expansion of cells that acquire genetic lesions over years. This model of cancer evolution based on ongoing genomic instability mechanism may apply to development of most MM cases. However, in a small fraction of newly diagnosed MM who relapse quickly and finally die within 2 years, the gradual model appears to be untenable. Analysis of high resolution copy number profiles obtained using single nucleotide polymorphism array data from 764 newly diagnosed MM identified large numbers of genomic rearrangements with the hallmarks of chromothripsis in 1.3% of samples. Moreover, this catastrophic event confers a poor outcome. Because chromothripsis appears to occur in a single crisis, our results suggest that high-risk MM patients use this novel way of cancer evolution.

MeSH Terms
Adult Aged Chromosome Breakage Gene Dosage/genetics Gene Rearrangement/genetics Genomic Instability/genetics Genomics Humans Middle Aged Molecular Sequence Data Multiple Myeloma/genetics,mortality Polymorphism, Single Nucleotide/genetics Risk Factors
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Magrangeas Florence
Inserm U892, Université de Nantes, Nantes, France.
Avet-Loiseau Hervé
Munshi Nikhil C
Minvielle Stéphane
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9 references, click to expand
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Article Info
Journal
Blood
Abbr.
Blood
ISSN
1528-0020
Published
2011-07-21
Epub
2011-00-31
Pages
675-8
Language
English
Region
United States
NLM ID
7603509
PMCID
PMC3142904
Subset
IM
Grants
NCI NIH HHS · P01 CA155258 · United States
NCI NIH HHS · R01 CA124929 · United States
NCI NIH HHS · P01 CA155258-01 · United States
Databases
GENBANK
GSE27560
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