MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia
Chih-Hsiang Yu, Tze-Kang Lin, Shiann‐Tarng Jou, Chien‐Yu Lin, Kai‐Hsin Lin, Meng‐Yao Lu, Shu-Huey Chen, Chao-Neng Cheng, Kang‐Hsi Wu, Shih-Chung Wang, Hsiu‐Hao Chang, Meng‐Ju Li, Yu-Ling Ni, Yi‐Ning Su, Dong‐Tsamn Lin, Hsuan‐Yu Chen, Christine J. Harrison, Chia-Cheng Hung, Shu‐Wha Lin, Yung‐Li Yang
Abstract
Abstract Aneuploidy occurs within a significant proportion of childhood B-cell acute lymphoblastic leukemia (B-ALL). Some copy number variations (CNV), associated with novel subtypes of childhood B-ALL, have prognostic significance. A total of 233 childhood B-ALL patients were enrolled into this study. Focal copy number alterations of ERG , IKZF1 , PAX5 , ETV6 , RB1 , BTG1 , EBF1 , CDKN2A / 2B , and the Xp22.33/Yp11.31 region were assessed by Multiplex Ligation-dependent Probe Amplification (MLPA). The MLPA telomere kit was used to identify aneuploidy through detection of whole chromosome loss or gain. We carried out these procedures alongside measurement of DNA index in order to identify, aneuploidy status in our cohort. MLPA telomere data and DNA index correlated well with aneuploidy status at higher sensitivity than cytogenetic analysis. Three masked hypodiploid patients, undetected by cytogenetics, and their associated copy number neutral loss of heterozygosity (CN-LOH) were identified by STR and SNP arrays. Rearrangements of TCF3 , located to 19p, were frequently associated with 19p deletions. Other genetic alterations including iAMP21, IKZF1 deletions, ERG deletions, PAX5 AMP , which have clinical significance or are associated with novel subtypes of ALL, were identified. In conclusion, appropriate application of MLPA aids the identifications of CNV and aneuploidy in childhood B-ALL.