Literature DB >> 25738466

Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis.

L Bassaganyas, S Beà, G Escaramís, C Tornador, I Salaverria, L Zapata, O Drechsel, P G Ferreira, B Rodriguez-Santiago, J M C Tubio, A Navarro, D Martín-García, C López, A Martínez-Trillos, A López-Guillermo, M Gut, S Ossowski, C López-Otín, E Campo, X Estivill.   

Abstract

Entities:  

Year:  2015        PMID: 25738466      PMCID: PMC5780638          DOI: 10.1038/leu.2014.309

Source DB:  PubMed          Journal:  Leukemia        ISSN: 0887-6924            Impact factor:   11.528


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Correction to: Leukemia (2013) 27, 2376–2379; doi:10.1038/leu.2013.127 Since the publication of this article, the authors have identified several errors within their paper. These are listed as follows: Table 1:
Table 1

Somatic point mutations in all time-point samples

ChromosomePositionReferenceObservedGeneExonic functionAAChange016-T00016-T02016-T05016-T11
178425887GAFUBP1stopgain SNVNM_003902:c.C1558T:p.Q541X++++
1186277552AGPRG4nonsynonymous SNVNM_001127710:c.A2299G:p.T901A++++
3141163154CTZBTB38nonsynonymous SNVNM_001080412:c.C1924T:p.P643S++++
644230329CANFKBIEstopgain SNVNM_004556:c.G853T:p.E285X+
6132892234ACTAAR6nonsynonymous SNVNM_175067:c.A774C:p.K258N++++
6146264389TCSHPRHnonsynonymous SNVNM_001042683:c.A2128G:p.M710V++++
11108114749GCATMnonsynonymous SNVNM_000051:c.G566C:p.R189T++++
1221358921CASLCO1B1nonsynonymous SNVNM_006446:c.C1451A:p.P484H++++
1545409873AGDUOXA1nonsynonymous SNVNM_144565:c.T1292C:p.V431A++++
16745751TCFBXL16nonsynonymous SNVNM_153350:c.A806G:p.N269S++++
1742463002GAITGA2Bnonsynonymous SNVNM_000419:c.C491T:p.A164V++++
1919431945GAMAU2splicing siteNA++++
1956173950ATU2AF2nonsynonymous SNVNM_001012478:c.A569T:p.Q190L+++
X125299321CADCAF12L2nonsynonymous SNVNM_001013628:c.G587T:p.W196L++++

+, present; −, absent.

Column ‘AAChange’: First row (without counting Header) should be NM_003902:c.C1558T:p.Q541X Second row should be NM_001127710:c.A2299G:p.T901A Third row should be NM_001080412:c.C1924T:p.P643S Supplementary Table S1: In the ‘ID sample’ column, ‘Sample Year’ 2006 is correct but ID sample should be 016-T06. Supplementary Table S3: Row 10 (without counting Header) column ‘locus’ should be t(1;10)(q32;q24). Row 24 (without counting Header) column ‘locus’ should be t(6;10)(q15;24). Row 50 (without counting Header) column ‘brk 2’ should be 19284700 and column ‘size’ should be 19166140. The corrected Table 1 is displayed here, and the corrected Supplementary Tables accompany the online version of this corrigendum. The authors would like to apologise for any inconvenience this may have caused.
  2 in total

1.  Frequent evolution of copy number alterations in CLL following first-line treatment with FC(R) is enriched with TP53 alterations: results from the CLL8 trial.

Authors:  J Edelmann; E Tausch; D A Landau; S Robrecht; J Bahlo; K Fischer; A M Fink; J Bloehdorn; K Holzmann; S Böttcher; L Werner; M Kneba; J G Gribben; D S Neuberg; C J Wu; M Hallek; H Döhner; S Stilgenbauer
Journal:  Leukemia       Date:  2016-11-02       Impact factor: 11.528

Review 2.  Next-generation sequencing in chronic lymphocytic leukemia: recent findings and new horizons.

Authors:  Ana E Rodríguez-Vicente; Vasilis Bikos; María Hernández-Sánchez; Jitka Malcikova; Jesús-María Hernández-Rivas; Sarka Pospisilova
Journal:  Oncotarget       Date:  2017-07-24
  2 in total

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