New concepts in the treatment of acute myeloid malignancies: Selected pathways for targeted therapy

Research output: Contribution to journalReview articlepeer-review

2 Scopus citations


Acute myeloid leukemia (AML) and myelodysplasia (MDS) continue to present formidable treatment challenges as there is not yet a "standard approach" that reliably and safely cures the majority of adults with these disorders. Understanding the basic cellular and molecular biology of leukemia is vital to the development of better treatment approaches. All malignant cells, including leukemias, carry survival advantages compared to their normal counterparts. These survival advantages are particularly evident when the cells face both normal environmental stressors as well as extreme stressors of potentially lethal DNA damage. The impact of such stressors is ultimately determined by the signaling pathways and resultant cellular activation, including alterations in cellular growth, differentiation, survival and death. It is our improving understanding of these signaling pathways, both normal and malignant, that provide the targets for novel therapies. In this review article, we will focus on several signaling pathways, as well as the regulation of the cell cycle, that not only represent potentially accessible sites for intervention in myeloid malignancies, but those that are actively being studied.

Original languageEnglish (US)
Pages (from-to)23-32
Number of pages10
JournalJournal of Biological Regulators and Homeostatic Agents
Issue number1-2
StatePublished - Jan 1 2005


  • Acute leukemia
  • Cell cycle regulation
  • Drug resistance
  • Molecular targets

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Immunology and Allergy
  • Physiology
  • Immunology
  • Oncology
  • Endocrinology
  • Physiology (medical)
  • Cancer Research


Dive into the research topics of 'New concepts in the treatment of acute myeloid malignancies: Selected pathways for targeted therapy'. Together they form a unique fingerprint.

Cite this