PKD1 inhibits cancer cells migration and invasion via Wnt signaling pathway in vitro

  • Ke Zhang
  • , Chun Ye
  • , Qin Zhou
  • , Rong Zheng
  • , Xiaoyan Lv
  • , Ye Chen
  • , Zhongguo Hu
  • , Hong Guo
  • , Zheng Zhang
  • , Yidong Wang
  • , Ruizhi Tan
  • , Yuhang Liu

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

The ∼14 kb mRNA of the polycystic kidney disease gene PKD1 encodes a large (∼460 kDa) protein, termed polycystin-1 (PC-1), that is responsible for autosomal dominant polycystic kidney disease (ADPKD). The unique organization of its multiple adhesive domains (16 Ig-like domains/PKD domains) suggests that it may play an important role in cell-cell/cell-matrix interactions. Here we demonstrated that PKD1 promoted cell-cell and cell-matrix interactions in cancer cells, indicating that PC-1 is involved in the cell adhesion process. Furthermore in this study, we showed that PKD1 inhibited cancer cells migration and invasion. And we also showed that PC-1 regulated these processes in a process that may be at least partially through the Wnt pathway. Collectively, our data suggest that PKD1 may act as a novel member of the tumor suppressor family of genes.

Original languageEnglish
Pages (from-to)767-774
Number of pages8
JournalCell Biochemistry and Function
Volume25
Issue number6
DOIs
StatePublished - Nov 2007
Externally publishedYes

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

  • Cell migration
  • Invasion
  • PKD1 gene
  • Wnt signaling pathway

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