The function of cyclic-adenosine monophosphate responsive element-binding protein in hematologic malignancies

Leuk Lymphoma. 2011 Nov;52(11):2057-63. doi: 10.3109/10428194.2011.584994.

Abstract

Central to discovering novel approaches to treating leukemias and lymphomas is a clear understanding of the signaling networks which lead to unchecked cell cycle progression, proliferation, and survival. Cyclic-adenosine monophosphate (cAMP) responsive element-binding protein (CREB) represents a critical integrator of numerous signals from cytoplasmic kinase cascades, and is directly involved in controlling the transcription of genes critical for normal cellular proliferation and survival. Several lines of evidence implicate CREB as a proto-oncogene, as a number of translocations involving CREB and dysregulation of expression are both associated with oncogenesis. Thus, CREB represents a potential therapeutic target in leukemia. Here, we review CREB function and regulation in normal and aberrant hematopoiesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Cell Survival / genetics
  • Cyclic AMP Response Element-Binding Protein / genetics
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Cyclic AMP Response Element-Binding Protein / physiology*
  • Gene Expression Regulation, Neoplastic
  • Hematologic Neoplasms / genetics
  • Hematologic Neoplasms / metabolism
  • Hematologic Neoplasms / physiopathology*
  • Hematopoiesis / genetics
  • Hematopoiesis / physiology*
  • Humans
  • Phosphorylation
  • Proto-Oncogene Mas
  • Signal Transduction / genetics
  • Signal Transduction / physiology*

Substances

  • Cyclic AMP Response Element-Binding Protein
  • MAS1 protein, human
  • Proto-Oncogene Mas