TY - JOUR
T1 - Advances in B-lymphoblastic leukemia
T2 - cytogenetic and genomic lesions
AU - Zhou, Yi
AU - Kanagal Shamanna, Rashmi
AU - Zuo, Zhuang
AU - Tang, Guilin
AU - Medeiros, L Jeffrey
AU - Bueso-Ramos, Carlos E
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/8/1
Y1 - 2016/8/1
N2 - The genomic profiling of B-cell lymphoblastic leukemia (B-ALL) subtypes are characterized by a constellation of genetic changes involving structural rearrangements, submicroscopic DNA copy number alterations, and sequence mutations. Several of these genetic changes have relevant implications for risk stratification and targeted therapeutic interventions. In this review, we summarize some of the well-known and recently identified genomic risk factors for B-ALL, with emphasis on their associated prognoses and methods of detection. Alterations in genes that regulate B-cell development are hallmarks of B-ALL. In particular, deletions of IKZF1, a gene determining early lymphoid differentiation, are associated with high-risk Ph + and Ph-like B-ALL subtypes. About 20% of B-ALL patients harbor genetic alterations that result in aberrant activation of protein tyrosine kinases. The genetic alterations include rearrangements of the cytokine receptor gene CRLF2; rearrangements of ABL1, JAK2, and PDGFRB; and mutations of JAK1 and JAK2. B-ALL with these genetic alterations may respond to targeted therapy using tyrosine kinase inhibitors. Recurrent genetic alterations involving TP53, CREBBP, and NT5C2 are enriched in relapsed B-ALL and may confer drug resistance. Future challenges include implementing genomic profiling into the clinic to guide risk stratification and the use of targeted therapies.
AB - The genomic profiling of B-cell lymphoblastic leukemia (B-ALL) subtypes are characterized by a constellation of genetic changes involving structural rearrangements, submicroscopic DNA copy number alterations, and sequence mutations. Several of these genetic changes have relevant implications for risk stratification and targeted therapeutic interventions. In this review, we summarize some of the well-known and recently identified genomic risk factors for B-ALL, with emphasis on their associated prognoses and methods of detection. Alterations in genes that regulate B-cell development are hallmarks of B-ALL. In particular, deletions of IKZF1, a gene determining early lymphoid differentiation, are associated with high-risk Ph + and Ph-like B-ALL subtypes. About 20% of B-ALL patients harbor genetic alterations that result in aberrant activation of protein tyrosine kinases. The genetic alterations include rearrangements of the cytokine receptor gene CRLF2; rearrangements of ABL1, JAK2, and PDGFRB; and mutations of JAK1 and JAK2. B-ALL with these genetic alterations may respond to targeted therapy using tyrosine kinase inhibitors. Recurrent genetic alterations involving TP53, CREBBP, and NT5C2 are enriched in relapsed B-ALL and may confer drug resistance. Future challenges include implementing genomic profiling into the clinic to guide risk stratification and the use of targeted therapies.
KW - B-cell development
KW - B-cell lymphoblastic leukemia
KW - Clonal evolution
KW - Genomic
KW - Molecular pathology
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U2 - 10.1016/j.anndiagpath.2016.02.002
DO - 10.1016/j.anndiagpath.2016.02.002
M3 - Review article
C2 - 27130145
AN - SCOPUS:84964587604
SN - 1092-9134
VL - 23
SP - 43
EP - 50
JO - Annals of Diagnostic Pathology
JF - Annals of Diagnostic Pathology
ER -