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Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization

Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization
Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization
Chromosomal abnormalities are important for the classification and risk stratification of patients with acute lymphoblastic leukemia (ALL). However, approximately 30% of childhood and 50% of adult patients lack abnormalities with clinical relevance. Here, we describe the use of array-based comparative genomic hybridization (aCGH) to identify copy number alterations (CNA) in 58 ALL patients. CNA were identified in 83% of cases, and most frequently involved chromosomes 21 (n=42), 9 (n=21), 6 (n=16), 12 (n=11), 15 (n=11), 8 (n=10) and 17 (n=10). Deletions of 6q (del(6q)) were heterogeneous in size, in agreement with previous data, demonstrating the sensitivity of aCGH to measure CNA. Although 9p deletions showed considerable variability in both the extent and location, all encompassed the CDKN2A locus. Six patients showed del(12p), with a common region encompassing the ETV6 gene. Complex CNA were observed involving chromosomes 6 (n=2), 15 (n=2) and 21 (n=11) with multiple regions of loss and gain along each chromosome. Chromosome 21 CNA shared a common region of gain, with associated subtelomeric deletions. Other recurrent findings included dim(13q), dim(16q) and enh(17q). This is the first report of genome-wide detection of CNA in ALL patients using aCGH, and it has demonstrated a higher level of karyotype complexity than anticipated from conventional cytogenetic analysis.
0950-9232
4306-4318
Strefford, J.C.
3782b392-f080-42bf-bdca-8aa5d6ca532f
Worley, H.
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Barber, K.
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Wright, S.
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Stewart, A.R.M.
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Robinson, H.M.
c406aa02-ca17-4ba1-9aa4-24bab6415fc0
Bettney, G.
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van Delft, F.W.
b658ff18-a440-4e41-accc-e6ddf8103c5d
Atherton, M.G.
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Davies, T.
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Griffiths, M.
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Hing, S.
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Ross, F.M.
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Talley, P.
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Saha, V.
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Moorman, A.V.
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Harrison, C.J.
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Strefford, J.C.
3782b392-f080-42bf-bdca-8aa5d6ca532f
Worley, H.
33e0cd81-d45f-49bc-9539-09345d79d895
Barber, K.
749c5845-4515-4a36-b7fb-cdc6ec29e984
Wright, S.
7dc41855-33fc-45d2-ab05-94731436da96
Stewart, A.R.M.
d7af25a1-53aa-4fa8-b6ff-addbb19f3b53
Robinson, H.M.
c406aa02-ca17-4ba1-9aa4-24bab6415fc0
Bettney, G.
356c3be7-67cd-436f-94a6-f3d130b3fd27
van Delft, F.W.
b658ff18-a440-4e41-accc-e6ddf8103c5d
Atherton, M.G.
0c5d9a59-529e-4091-99a7-c162db02a406
Davies, T.
3136debe-8502-4559-9b01-5f8e5f8f6af7
Griffiths, M.
bee8f9b6-9d6c-43f8-babb-abaf89ab503a
Hing, S.
da3566e8-ba96-4393-9232-91bc73e431d5
Ross, F.M.
ec0958f8-b992-4e4a-b7e3-c474600390ba
Talley, P.
95b1c17c-eb98-4aab-bf0d-b4ef81ac96e4
Saha, V.
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Moorman, A.V.
af5027f3-4927-4e62-b1be-ac4bdcf6cd8f
Harrison, C.J.
9c9f6b47-8bfc-49dd-b156-74539b170291

Strefford, J.C., Worley, H., Barber, K., Wright, S., Stewart, A.R.M., Robinson, H.M., Bettney, G., van Delft, F.W., Atherton, M.G., Davies, T., Griffiths, M., Hing, S., Ross, F.M., Talley, P., Saha, V., Moorman, A.V. and Harrison, C.J. (2007) Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization. Oncogene, 26 (29), 4306-4318. (doi:10.1038/sj.onc.1210190).

Record type: Article

Abstract

Chromosomal abnormalities are important for the classification and risk stratification of patients with acute lymphoblastic leukemia (ALL). However, approximately 30% of childhood and 50% of adult patients lack abnormalities with clinical relevance. Here, we describe the use of array-based comparative genomic hybridization (aCGH) to identify copy number alterations (CNA) in 58 ALL patients. CNA were identified in 83% of cases, and most frequently involved chromosomes 21 (n=42), 9 (n=21), 6 (n=16), 12 (n=11), 15 (n=11), 8 (n=10) and 17 (n=10). Deletions of 6q (del(6q)) were heterogeneous in size, in agreement with previous data, demonstrating the sensitivity of aCGH to measure CNA. Although 9p deletions showed considerable variability in both the extent and location, all encompassed the CDKN2A locus. Six patients showed del(12p), with a common region encompassing the ETV6 gene. Complex CNA were observed involving chromosomes 6 (n=2), 15 (n=2) and 21 (n=11) with multiple regions of loss and gain along each chromosome. Chromosome 21 CNA shared a common region of gain, with associated subtelomeric deletions. Other recurrent findings included dim(13q), dim(16q) and enh(17q). This is the first report of genome-wide detection of CNA in ALL patients using aCGH, and it has demonstrated a higher level of karyotype complexity than anticipated from conventional cytogenetic analysis.

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Published date: 2007

Identifiers

Local EPrints ID: 44618
URI: http://eprints.soton.ac.uk/id/eprint/44618
ISSN: 0950-9232
PURE UUID: a90032b6-bbe6-4641-8c58-b0b8a857d3a1
ORCID for J.C. Strefford: ORCID iD orcid.org/0000-0002-0972-2881
ORCID for H. Worley: ORCID iD orcid.org/0000-0001-8308-9781

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Date deposited: 06 Mar 2007
Last modified: 16 Mar 2024 03:40

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Contributors

Author: J.C. Strefford ORCID iD
Author: H. Worley ORCID iD
Author: K. Barber
Author: S. Wright
Author: A.R.M. Stewart
Author: H.M. Robinson
Author: G. Bettney
Author: F.W. van Delft
Author: M.G. Atherton
Author: T. Davies
Author: M. Griffiths
Author: S. Hing
Author: F.M. Ross
Author: P. Talley
Author: V. Saha
Author: A.V. Moorman
Author: C.J. Harrison

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