Arl13b Promotes Gastric Tumorigenesis by Regulating Smo Trafficking and Activation of the Hedgehog Signaling Pathway

Cancer Res. 2017 Aug 1;77(15):4000-4013. doi: 10.1158/0008-5472.CAN-16-2461. Epub 2017 Jun 13.

Abstract

Inhibitors of the Hedgehog (Hh) pathway transducer Smoothened (Smo) have been approved for cancer treatment, but Smo mutations often lead to tumor resistance and it remains unclear how Smo is regulated. In this study, we identified the small GTPase Arl13b as a novel partner and regulator of Smo. Arl13b regulated Smo stability, trafficking, and localization, which are each crucial for Hh signaling. In gastric cancer cells, Arl13b stimulated proliferation, migration, and invasion in vitro and in vivo In clinical specimens of gastric cancer, Arl13b expression correlated strongly with tumor size and depth of invasion; patients with high levels of Arl13b had a poor prognosis. Our results show how Arl13b participates in Hh pathway activation in gastric cancer. Cancer Res; 77(15); 4000-13. ©2017 AACR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-Ribosylation Factors / metabolism*
  • Adult
  • Aged
  • Animals
  • Blotting, Western
  • Carcinogenesis / metabolism*
  • Female
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Hedgehog Proteins / metabolism
  • Heterografts
  • Humans
  • Immunohistochemistry
  • Male
  • Mice
  • Middle Aged
  • Protein Transport / physiology
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction / physiology
  • Smoothened Receptor / metabolism*
  • Stomach Neoplasms / metabolism
  • Stomach Neoplasms / pathology*

Substances

  • Hedgehog Proteins
  • SMO protein, human
  • Smoothened Receptor
  • ADP-Ribosylation Factors
  • ARL13B protein, human