Research
Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis
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* Corresponding author: Lisa G Shaffer lisa.shaffer@perkinelmer.com
1 Signature Genomics, 2820 N. Astor St., Spokane, WA, 99207, USA
2 Department of Hematology/Hematopoietic Cell Transplantation, City of Hope, 1500 E. Duarte Rd., Duarte, CA, 91010, USA
3 Department of Pathology, City of Hope, 1500 E. Duarte Rd., Duarte, CA, 91010, USA
4 Department of Cytogenetics, City of Hope, 1500 E. Duarte Rd., Duarte, CA, 91010, USA
5 Department of Biostatistics, City of Hope, 1500 E. Duarte Rd., Duarte, CA, 91010, USA
6 Quest Diagnostics Nichols Institute, Chantilly, VA, USA
Molecular Cytogenetics 2011, 4:4 doi:10.1186/1755-8166-4-4
Published: 3 February 2011Abstract
Background
Chronic lymphocytic leukemia (CLL) is a highly variable disease with life expectancies ranging from months to decades. Cytogenetic findings play an integral role in defining the prognostic significance and treatment for individual patients.
Results
We have evaluated 25 clinical cases from a tertiary cancer center that have an established diagnosis of CLL and for which there was prior cytogenetic and/or fluorescence in situ hybridization (FISH) data. We performed microarray-based comparative genomic hybridization (aCGH) using a bacterial artificial chromosome (BAC)-based microarray designed for the detection of known constitutional genetic syndromes. In 15 of the 25 cases, aCGH detected all copy number imbalances identified by prior cytogenetic and/or FISH studies. For the majority of those not detected, the aberrations were present at low levels of mosaicism. Furthermore, for 15 of the 25 cases, additional abnormalities were detected. Four of those cases had deletions that mapped to intervals implicated in inherited predisposition to CLL. For most cases, aCGH was able to detect abnormalities present in as few as 10% of cells. Although changes in ploidy are not easily discernable by aCGH, results for two cases illustrate the detection of additional copy gains and losses present within a mosaic tetraploid cell population.
Conclusions
Our results illustrate the successful evaluation of CLL using a microarray optimized for the interrogation of inherited disorders and the identification of alterations with possible relevance to CLL susceptibility.