Literature DB >> 26178348

Pathways to chromothripsis.

Robert Ivkov1, Fred Bunz1.   

Abstract

Chromothripsis is a recently recognized mode of genetic instability that generates chromosomes with strikingly large numbers of segmental re-arrangements. While the characterization of these derivative chromosomes has provided new insights into the processes by which cancer genomes can evolve, the underlying signaling events and molecular mechanisms remain unknown. In medulloblastomas, chromothripsis has been observed to occur in the context of mutational inactivation of p53 and activation of the canonical Hedgehog (Hh) pathway. Recent studies have illuminated mechanistic links between these 2 signaling pathways, including a novel PTCH1 homolog that is regulated by p53. Here, we integrate this new pathway into a hypothetical model for the catastrophic DNA breakage that appears to trigger profound chromosomal rearrangements.

Entities:  

Keywords:  PTCH53; chromothripsis; hedgehog; medulloblastoma; p53

Mesh:

Substances:

Year:  2015        PMID: 26178348      PMCID: PMC4825555          DOI: 10.1080/15384101.2015.1068483

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  30 in total

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Journal:  Nature       Date:  2006-12-06       Impact factor: 49.962

2.  Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.

Authors:  Tobias Rausch; David T W Jones; Marc Zapatka; Adrian M Stütz; Thomas Zichner; Joachim Weischenfeldt; Natalie Jäger; Marc Remke; David Shih; Paul A Northcott; Elke Pfaff; Jelena Tica; Qi Wang; Luca Massimi; Hendrik Witt; Sebastian Bender; Sabrina Pleier; Huriye Cin; Cynthia Hawkins; Christian Beck; Andreas von Deimling; Volkmar Hans; Benedikt Brors; Roland Eils; Wolfram Scheurlen; Jonathon Blake; Vladimir Benes; Andreas E Kulozik; Olaf Witt; Dianna Martin; Cindy Zhang; Rinnat Porat; Diana M Merino; Jonathan Wasserman; Nada Jabado; Adam Fontebasso; Lars Bullinger; Frank G Rücker; Konstanze Döhner; Hartmut Döhner; Jan Koster; Jan J Molenaar; Rogier Versteeg; Marcel Kool; Uri Tabori; David Malkin; Andrey Korshunov; Michael D Taylor; Peter Lichter; Stefan M Pfister; Jan O Korbel
Journal:  Cell       Date:  2012-01-20       Impact factor: 41.582

3.  WIP1 phosphatase modulates the Hedgehog signaling by enhancing GLI1 function.

Authors:  S Pandolfi; V Montagnani; J Y Penachioni; M C Vinci; B Olivito; L Borgognoni; B Stecca
Journal:  Oncogene       Date:  2012-11-12       Impact factor: 9.867

4.  Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint.

Authors:  Q Liu; S Guntuku; X S Cui; S Matsuoka; D Cortez; K Tamai; G Luo; S Carattini-Rivera; F DeMayo; A Bradley; L A Donehower; S J Elledge
Journal:  Genes Dev       Date:  2000-06-15       Impact factor: 11.361

5.  Altered neural cell fates and medulloblastoma in mouse patched mutants.

Authors:  L V Goodrich; L Milenković; K M Higgins; M P Scott
Journal:  Science       Date:  1997-08-22       Impact factor: 47.728

6.  A GLI1-p53 inhibitory loop controls neural stem cell and tumour cell numbers.

Authors:  Barbara Stecca; Ariel Ruiz i Altaba
Journal:  EMBO J       Date:  2009-02-12       Impact factor: 11.598

7.  Essential function of Chk1 can be uncoupled from DNA damage checkpoint and replication control.

Authors:  Deborah Wilsker; Eva Petermann; Thomas Helleday; Fred Bunz
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-17       Impact factor: 11.205

8.  Chk1 is haploinsufficient for multiple functions critical to tumor suppression.

Authors:  Michael H Lam; Qinghua Liu; Stephen J Elledge; Jeffrey M Rosen
Journal:  Cancer Cell       Date:  2004-07       Impact factor: 31.743

9.  Massive genomic rearrangement acquired in a single catastrophic event during cancer development.

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Journal:  Cell       Date:  2011-01-07       Impact factor: 41.582

10.  Sonic Hedgehog signaling impairs ionizing radiation-induced checkpoint activation and induces genomic instability.

Authors:  Jennifer M Leonard; Hong Ye; Cynthia Wetmore; Larry M Karnitz
Journal:  J Cell Biol       Date:  2008-10-27       Impact factor: 10.539

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  4 in total

Review 1.  Chromothripsis, a credible chromosomal mechanism in evolutionary process.

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Journal:  Chromosoma       Date:  2018-08-07       Impact factor: 4.316

2.  Origin and Evolution of Diploid and Allopolyploid Camelina Genomes Were Accompanied by Chromosome Shattering.

Authors:  Terezie Mandáková; Milan Pouch; Jordan R Brock; Ihsan A Al-Shehbaz; Martin A Lysak
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Review 3.  The Tip of an Iceberg: Replication-Associated Functions of the Tumor Suppressor p53.

Authors:  Vanesa Gottifredi; Lisa Wiesmüller
Journal:  Cancers (Basel)       Date:  2018-07-28       Impact factor: 6.639

Review 4.  Chromothripsis in Chronic Lymphocytic Leukemia: A Driving Force of Genome Instability.

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