Current insights into the role of Fli-1 in hematopoiesis and malignant transformation

Cell Mol Life Sci. 2022 Feb 28;79(3):163. doi: 10.1007/s00018-022-04160-1.

Abstract

Fli-1, a member of the ETS family of transcription factors, was discovered in 1991 through retroviral insertional mutagenesis as a driver of mouse erythroleukemias. In the past 30 years, nearly 2000 papers have defined its biology and impact on normal development and cancer. In the hematopoietic system, Fli-1 controls self-renewal of stem cells and their differentiation into diverse mature blood cells. Fli-1 also controls endothelial survival and vasculogenesis, and high and low levels of Fli-1 are implicated in the auto-immune diseases systemic lupus erythematosus and systemic sclerosis, respectively. In addition, aberrant Fli-1 expression is observed in, and is essential for, the growth of multiple hematological malignancies and solid cancers. Here, we review the historical context and latest research on Fli-1, focusing on its role in hematopoiesis, immune response, and malignant transformation. The importance of identifying Fli-1 modulators (both agonists and antagonists) and their potential clinical applications is discussed.

Keywords: Cancer; ETS family; Erythropoiesis; FLI1; Hematopoiesis; Leukemia; Megakaryopoiesis.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Transformation, Neoplastic / genetics
  • Hematopoiesis / genetics
  • Leukemia, Erythroblastic, Acute* / pathology
  • Mice
  • Proto-Oncogene Protein c-fli-1* / genetics
  • Proto-Oncogene Protein c-fli-1* / metabolism

Substances

  • Proto-Oncogene Protein c-fli-1