Somatic mutations of the β-TrCP gene in gastric cancer

  • Chang Jae Kim
  • , Jae Hwi Song
  • , Yong Gu Cho
  • , Young Sill Kim
  • , Su Young Kim
  • , Suk Woo Nam
  • , Nam Jin Yoo
  • , Jung Young Lee
  • , Won Sang Park

Research output: Contribution to journalArticlepeer-review

49 Scopus citations

Abstract

Beta-TrCP is a component of the ubiquitin ligase complex targeting β-catenin for proteasomal degradation, and is a negative regulator of Wnt/β-catenin signaling. To determine whether genetic alterations of the β-TrCP gene are involved in the development or progression of gastric cancer, we analyzed its somatic mutations in 95 gastric cancers by single-strand conformational polymorphism and sequencing. We found five missense mutations (5.3%): A99V, H342Y, H425Y, C206Y, and G260E. Tissue carrying mutations showed moderate to strong cytoplasmic and/or nuclear staining of β-catenin by immunohistochemistry. Thus, somatic mutations of the β-TrCP gene may contribute to the development of gastric cancer through β-catenin stabilization.

Original languageEnglish
Pages (from-to)127-133
Number of pages7
JournalAPMIS
Volume115
Issue number2
DOIs
StatePublished - Feb 2007

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Beta-catenin
  • Gastric cancer
  • Immunohistochemistry
  • Mutation
  • Wnt signal

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