Deregulated TGF-β signaling in leukemogenesis

Hui Kuan Lin, Stephan Bergmann, Pier Paolo Pandolfi

Research output: Contribution to journalReview articlepeer-review

43 Scopus citations

Abstract

Cellular homeostasis is tightly controlled by the various pathways that regulate cell proliferation and cell death. Breaking this balance is often associated with cancer development. The transforming growth factor-β (TGF-β) pathway plays an important role in cellular homeostasis by regulating cell growth inhibition, cellular senescence, differentiation and apoptosis. Deregulated TGF-β signaling is known to be involved in a variety of human cancers, including those of the colon, pancreas, breast and prostate. While TGF-β is a potent negative regulator of hematopoiesis, the role of aberrant TGF-β signaling in leukemogenesis remains largely unknown. Recently, evidence demonstrating deregulated TGF-β signaling in leukemogenesis, particularly in acute promyelocytic leukemia (APL), has started to emerge. In this review, we summarize the current progress towards the understanding of the molecular mechanisms by which aberrant TGF-β signaling may participate in leukemogenesis.

Original languageEnglish (US)
Pages (from-to)5693-5700
Number of pages8
JournalOncogene
Volume24
Issue number37
DOIs
StatePublished - Aug 29 2005

Keywords

  • PML-RARα
  • SARA
  • Smad2/3
  • TGF-β
  • cPML

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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