Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Acquisition of genome-wide copy number alterations in monozygotic twins with acute lymphoblastic leukemia

Bateman, Caroline M., Colman, Susan M., Chaplin, Tracy, Young, Bryan D., Eden, Tim O., Bhakta, Manoo, Gratias, Eric J., van Wering, Elisbeth R., Cazzaniga, Gianni, Harrison, Christine J., Hain, Richard D. W., Ancliff, Philip, Ford, Anthony M., Kearney, Lyndal and Greaves, Mel 2010. Acquisition of genome-wide copy number alterations in monozygotic twins with acute lymphoblastic leukemia. Blood 115 (17) , pp. 3553-3558. 10.1182/blood-2009-10-251413

Full text not available from this repository.


Chimaeric fusion genes are highly prevalent in childhood acute lymphoblastic leukaemia (ALL) and are mostly pre-natal, early genetic events in the evolutionary trajectory of this cancer. ETV6-RUNX1-positive ALL also has multiple (~six per case) copy number alterations (CNA) as revealed by genome-wide SNP arrays. Recurrent CNA are probably 'driver' events contributing critically to clonal diversification and selection but, at diagnosis, their developmental timing is 'buried' in the leukaemia's covert natural history. This conundrum can be resolved with twin pairs. We identified and compared CNA in five pairs of monozygotic twins with concordant ETV6-RUNX1-positive ALL and one pair discordant for ETV6-RUNX1 positive ALL. We compared, within each pair, CNA classified as potential 'driver' or 'passenger' mutations based upon recurrency and, where known, gene function. An average of 5.1 (range 3-11) CNAs (excluding immunoglobulin/T-cell receptor alterations) were identified per case. All 'driver' CNA (total 32) were distinct within each of the five twin pairs with concordant ALL. 'Driver' CNA in another twin with ALL were all absent in the shared ETV6-RUNX1-positive pre-leukaemic clone of her healthy co-twin. These data place all 'driver' CNA secondary to the pre-natal gene fusion event and most probably post-natal in the sequential, molecular pathogenesis of ALL.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Subjects: R Medicine > RC Internal medicine > RC0254 Neoplasms. Tumors. Oncology (including Cancer)
Publisher: American Society of Hematology
ISSN: 0006-4971
Last Modified: 19 Mar 2016 22:49

Citation Data

Cited 72 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item