Overexpression of dopamine receptor D2 promotes colorectal cancer progression by activating the β-catenin/ZEB1 axis

Cancer Sci. 2021 Sep;112(9):3732-3743. doi: 10.1111/cas.15026. Epub 2021 Jul 4.

Abstract

Colorectal cancer (CRC) is a recurring cancer that is often resistant to conventional therapies and therefore requires the development of molecular-based therapeutic approaches. Dopamine receptor D2 (DRD2) is associated with the growth of many types of tumors, but its oncogenic role in CRC is unclear. Here, we observed that elevated DRD2 expression was associated with a poor survival rate among patients with CRC. Depletion of DRD2 suppressed CRC cell growth and motility by downregulating β-catenin/ZEB signaling in vitro and in vivo, whereas overexpression of DRD2 promoted CRC cell progression. Inhibition of DRD2 by the antagonist pimozide inhibited tumor growth and lymph node metastasis in vivo and enhanced the cytotoxic effects of conventional agents in vitro. Taken together, our findings indicate that targeting the DRD2/β-catenin/ZEB1 signaling axis is a potentially promising therapeutic strategy for patients with CRC.

Keywords: DRD2; ZEB1; colorectal cancer; metastasis; pimozide.

Publication types

  • Retracted Publication

MeSH terms

  • Aged
  • Animals
  • Cell Movement / genetics
  • Cell Proliferation / drug effects
  • Cell Proliferation / genetics
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / mortality*
  • Colorectal Neoplasms / pathology
  • Disease Progression*
  • Dopamine Antagonists / pharmacology
  • Female
  • HCT116 Cells
  • HT29 Cells
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Middle Aged
  • Pimozide / pharmacology
  • RNA Interference
  • Receptors, Dopamine D2 / genetics
  • Receptors, Dopamine D2 / metabolism*
  • Signal Transduction
  • Survival Rate
  • Transfection
  • Tumor Burden / drug effects
  • Tumor Burden / genetics
  • Up-Regulation
  • Xenograft Model Antitumor Assays
  • Zinc Finger E-box-Binding Homeobox 1 / metabolism*
  • beta Catenin / metabolism*

Substances

  • CTNNB1 protein, human
  • DRD2 protein, human
  • Dopamine Antagonists
  • Receptors, Dopamine D2
  • ZEB1 protein, human
  • Zinc Finger E-box-Binding Homeobox 1
  • beta Catenin
  • Pimozide