TY - JOUR
T1 - New strategies in acute myeloid leukemia
T2 - Redefining prognostic markers to guide therapy
AU - Khan, Irum
AU - Altman, Jessica K.
AU - Licht, Jonathan D.
PY - 2012/10/1
Y1 - 2012/10/1
N2 - Although standard therapy for AML has been relatively constant over the past 2 decades, this may be changing with enhanced technologies allowing for the classification of acute myeloid leukemia (AML) into molecularly distinct subsets. Some specific subsets of AML have an excellent prognosis in response to standard therapy, whereas the poor prognosis of AML associated with specific sets of mutations or chromosomal anomalies requires the development of new therapies. Elucidation of the molecular pathogenesis of AML has led to the development of therapies that affect signaling, apoptosis, protein and intermediate metabolism, the surface of the leukemia cell, leukemia cell/stromal interaction, and epigenetic regulation of gene expression.
AB - Although standard therapy for AML has been relatively constant over the past 2 decades, this may be changing with enhanced technologies allowing for the classification of acute myeloid leukemia (AML) into molecularly distinct subsets. Some specific subsets of AML have an excellent prognosis in response to standard therapy, whereas the poor prognosis of AML associated with specific sets of mutations or chromosomal anomalies requires the development of new therapies. Elucidation of the molecular pathogenesis of AML has led to the development of therapies that affect signaling, apoptosis, protein and intermediate metabolism, the surface of the leukemia cell, leukemia cell/stromal interaction, and epigenetic regulation of gene expression.
UR - http://www.scopus.com/inward/record.url?scp=84866911128&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84866911128&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-12-0313
DO - 10.1158/1078-0432.CCR-12-0313
M3 - Article
C2 - 22893630
AN - SCOPUS:84866911128
SN - 1078-0432
VL - 18
SP - 5163
EP - 5171
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 19
ER -