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Mitogen-activated protein kinases and Wnt/β-catenin signaling: Molecular conversations among signaling pathways

  • Stony Brook University

Research output: Contribution to journalReview articlepeer-review

79 Scopus citations

Abstract

Wnt/β-catenin canonical pathway is critical for normal embryonic development; mutations and aberrant expression of specific components of this pathway can be oncogenic, Mitogen-activated protein kinase (MAPK) pathways, prominent in intracellular signaling, have been shown to have unique and provocative roles that impact the Wnt/β-catenin signaling. We discuss recent insights that implicate the three major pathways of the MAPK network, i.e., mediated by p38, c-Jun N-terminal (JNK) kinase and Extra-cellular- Regulated Kinases (ERK) and their downstream signaling elements in Wnt/β-catenin signaling. Novel "crosstalk" among MAPK and Wnt/β-catenin canonical signaling pathways is essential. A fuller understanding of how such signaling is integrated during development is a high-value target for future research.

Original languageEnglish
Pages (from-to)46-49
Number of pages4
JournalCommunicative and Integrative Biology
Volume2
Issue number1
DOIs
StatePublished - 2009

Keywords

  • Dishevelled
  • ERK
  • Frizzled
  • G-protein
  • JNK
  • Lef/Tcf
  • p38
  • Wnt
  • β-catenin

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