Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia
Date
2012Author
Akçay, Arzu
Türkkan, Emine
Oztunc, Ceren
Yildiz, Inci
Anak, Sema
Devecioglu, Omer
Hatirnaz, Ozden
Celkan, Tiraje
Unuvar, Aysegul
Sayitoglu, Müge
Karaman, SERAP
Cinar, Suzan
Timur, Cetin
AYDOGAN, Gonul
Atay, Didem
ORHANER, Betul
Sarper, Nazan
Deniz, Gunnur
Ozbek, Ugur
Firtina, Sinem
Erbilgin, Yucel
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Show full item recordAbstract
B-lineage acute lymphoblastic leukemia (B-ALL) is a common subtype of acute leukemia in children. PAX5 plays a central role in B-cell development and differentiation. In this study, we analyzed PAX5 expression levels, transactivation domain mutations/deletions in B-ALL patients (n = 115) and healthy controls (n = 10). Relative PAX5 mRNA levels were significantly increased in B-ALL patients (p < 0.0001). PAX5 expression was also evaluated in three different B-ALL subgroups (pro B, Common B and Pre B ALL) and showed stage specific expression levels. Pro B (p = 0.04) and pre B (p = 0.04) patients showed significantly high PAX5 mRNA levels compared to stage specific controls. At least one deletion of exons 7-8 or 9 has been identified in the 41% of the patients. CD34 positivity in patients and presence of large deletions (Delta 7/8/9) showed a significant correlation (p = 0.05). None of our patients showed PAX5 point mutations, but two previously identified SNPs (rs3780135 and rs35469494) were detected. Our results support that PAX5 is a critical factor in B-ALL development and aberrant PAX5 expression especially at early stages may leads to leukemic transformation. (C) 2011 Elsevier Ltd. All rights reserved.
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