Genetic and epigenetic heterogeneity and the impact on cancer relapse.
Document Type
Article
Publication Date
10-2017
JAX Source
Exp Hematol 2017 Oct; 54:26-30
Volume
54
First Page
26
Last Page
30
ISSN
1873-2399
PMID
28705639
DOI
https://doi.org/10.1016/j.exphem.2017.07.002
Abstract
Acute myeloid leukemia (AML) is an aggressive hematopoietic malignancy with an exceedingly poor prognosis: a 5-year overall survival rate of 40%-45% in the young and a 5-year survival rate of less than 10% in the elderly (>60 years of age). Although a high percentage of patients enters complete remission after chemotherapeutic intervention, the majority of patients relapse within 3 years. Such stark prognostic outcomes highlight the need for additional clinical research, basic discovery, and molecular delineation of the etiologies and mechanisms behind responses to therapy that lead to relapse. Here, we summarize recent discoveries in tumor heterogeneity at the genetic and epigenetic levels and their independent molecular trajectories and dynamics in response to therapy. These new discoveries may have significant implications for understanding, monitoring, and treating leukemia and other cancers. Exp Hematol 2017 Oct; 54:26-30.
Recommended Citation
Hassan C,
Afshinnekoo E,
Li S,
Wu S,
Mason C.
Genetic and epigenetic heterogeneity and the impact on cancer relapse. Exp Hematol 2017 Oct; 54:26-30