Literature DB >> 25128687

Constitutional chromoanasynthesis: description of a rare chromosomal event in a patient.

Julie Plaisancié1, Pascale Kleinfinger2, Claude Cances3, Anne Bazin2, Sophie Julia4, Detlef Trost2, Laurence Lohmann2, Adeline Vigouroux5.   

Abstract

Structural alterations in chromosomes are a frequent cause of cancers and congenital diseases. Recently, the phenomenon of chromosome crisis, consisting of a set of tens to hundreds of clustered genomic rearrangements, localized in one or a few chromosomes, was described in cancer cells under the term chromothripsis. Better knowledge and recognition of this catastrophic chromosome event has brought to light two distinct entities, chromothripsis and chromoanasynthesis. The complexity of these rearrangements and the original descriptions in tumor cells initially led to the thought that it was an acquired anomaly. In fact, a few patients have been reported with constitutional chromothripsis or chromoanasynthesis. Using microarray we identified a very complex chromosomal rearrangement in a patient who had a cytogenetically visible rearrangement of chromosome 18. The rearrangement contained more than 15 breakpoints localized on a single chromosome. Our patient displayed intellectual disability, behavioral troubles and craniofacial dysmorphism. Interestingly, the succession of duplications and triplications identified in our patient was not clustered on a single chromosomal region but spread over the entire chromosome 18. In the light of this new spectrum of chromosomal rearrangements, this report outlines the main features of these catastrophic events and discusses the underlying mechanism of the complex chromosomal rearrangement identified in our patient, which is strongly evocative of a chromoanasynthesis.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Chromoanasynthesis; Chromothripsis; Complex chromosomal rearrangement; FoSTes; MMBIR

Mesh:

Year:  2014        PMID: 25128687     DOI: 10.1016/j.ejmg.2014.07.004

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  9 in total

1.  Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies.

Authors:  Bruno Faulin Gamba; Antônio Richieri-Costa; Silvia Costa; Carla Rosenberg; Lucilene Arilho Ribeiro-Bicudo
Journal:  Mol Genet Genomics       Date:  2015-06-04       Impact factor: 3.291

2.  The Growing Complexity of the Monosomy 1p36 Syndrome.

Authors:  Martin Poot
Journal:  Mol Syndromol       Date:  2016-03-31

Review 3.  The Iceberg under Water: Unexplored Complexity of Chromoanagenesis in Congenital Disorders.

Authors:  Cinthya J Zepeda-Mendoza; Cynthia C Morton
Journal:  Am J Hum Genet       Date:  2019-04-04       Impact factor: 11.025

Review 4.  Human Structural Variation: Mechanisms of Chromosome Rearrangements.

Authors:  Brooke Weckselblatt; M Katharine Rudd
Journal:  Trends Genet       Date:  2015-07-22       Impact factor: 11.639

Review 5.  Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements.

Authors:  Martin Poot; Thomas Haaf
Journal:  Mol Syndromol       Date:  2015-08-15

6.  Mechanisms for Complex Chromosomal Insertions.

Authors:  Shen Gu; Przemyslaw Szafranski; Zeynep Coban Akdemir; Bo Yuan; Mitchell L Cooper; Maria A Magriñá; Carlos A Bacino; Seema R Lalani; Amy M Breman; Janice L Smith; Ankita Patel; Rodger H Song; Weimin Bi; Sau Wai Cheung; Claudia M B Carvalho; Paweł Stankiewicz; James R Lupski
Journal:  PLoS Genet       Date:  2016-11-23       Impact factor: 5.917

7.  Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.

Authors:  Ryan L Collins; Harrison Brand; Claire E Redin; Carrie Hanscom; Caroline Antolik; Matthew R Stone; Joseph T Glessner; Tamara Mason; Giulia Pregno; Naghmeh Dorrani; Giorgia Mandrile; Daniela Giachino; Danielle Perrin; Cole Walsh; Michelle Cipicchio; Maura Costello; Alexei Stortchevoi; Joon-Yong An; Benjamin B Currall; Catarina M Seabra; Ashok Ragavendran; Lauren Margolin; Julian A Martinez-Agosto; Diane Lucente; Brynn Levy; Stephan J Sanders; Ronald J Wapner; Fabiola Quintero-Rivera; Wigard Kloosterman; Michael E Talkowski
Journal:  Genome Biol       Date:  2017-03-06       Impact factor: 13.583

8.  Chromoanasynthesis is a common mechanism that leads to ERBB2 amplifications in a cohort of early stage HER2+ breast cancer samples.

Authors:  George Vasmatzis; Xue Wang; James B Smadbeck; Stephen J Murphy; Katherine B Geiersbach; Sarah H Johnson; Athanasios G Gaitatzes; Yan W Asmann; Farhad Kosari; Mitesh J Borad; Daniel J Serie; Sarah A McLaughlin; Jennifer M Kachergus; Brian M Necela; E Aubrey Thompson
Journal:  BMC Cancer       Date:  2018-07-13       Impact factor: 4.430

9.  Failure of NIPT to detect constitutional chromoanasynthesis involving chromosome 21 in a case of fetal hydrops-A case report.

Authors:  Kathleen Bone; Melissa Jean MacPherson; Judy Chernos; Julie Lauzon
Journal:  Clin Case Rep       Date:  2019-09-30
  9 in total

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