Genetic and epigenetic heterogeneity and the impact on cancer relapse. Review uri icon

Overview

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.

publication date

  • July 10, 2017

Research

keywords

  • Chromosome Aberrations
  • Epigenesis, Genetic
  • Gene Expression Regulation, Leukemic
  • Genetic Heterogeneity
  • Leukemia, Myeloid, Acute
  • Neoplasm Proteins

Identity

PubMed Central ID

  • PMC5651672

Scopus Document Identifier

  • 85028352858

Digital Object Identifier (DOI)

  • 10.1016/j.exphem.2017.07.002

PubMed ID

  • 28705639

Additional Document Info

volume

  • 54