Jab1 Silencing Inhibits Proliferation and Sensitizes to Cisplatin in Biliary Tract Cancer

Cancer Res Treat. 2019 Jul;51(3):886-900. doi: 10.4143/crt.2018.375. Epub 2018 Oct 1.

Abstract

Purpose: Jab1 is a coactivator of c-Jun that enhances the transcriptional function of c-Jun. Jab1 is frequently overexpressed in various cancers and is associatedwith poor prognosis of cancer patients. Thus, Jab1 could be a potential therapeutic target in cancer. However, the role of Jab1 in biliary tract cancer (BTC) has not been studied.

Materials and methods: We performed in vitro and in vivo experiments to evaluate the therapeutic potential ofJab1 inhibition in BTC.

Results: Among 8 BTC cell lines, many showed higher Jab1 expression levels. In addition, Jab1 silencing by siRNA increased p27 expression levels. SNU478 and HuCCT-1 cells exhibited profound Jab1 knockdown and increased p27 expression by Jab1-specific siRNA transfection. Jab1 silencing induced anti-proliferative and anti-migratory effects and resulted in G1 cell cycle arrest in SNU478 and HuCCT-1 cells. In addition, Jab1 silencing potentiated the anti-proliferative and anti-migratory effects of cisplatin by increasing DNA damage. Interestingly,Jab1 knockdown increased PTEN protein half-life, resulting in increased PTEN expression. In the HuCCT-1 mouse xenograft model, stable knockdown of Jab1 by shRNA also showed anti-proliferative effects in vivo, with decreased Ki-67 expression and AKT phosphorylation and increased Terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling and p27 expression.

Conclusion: Jab1 knockdown demonstrated anti-proliferative and anti-migratory effects in BTC cells by increasing DNA damage and stabilizing PTEN, resulting in G1 cell cycle arrest. In addition, Jab1 silencing potentiated the anti-proliferative effects of cisplatin. Our data suggest that Jab1 may be a potential therapeutic target in BTC that is worthy of further investigations.

Keywords: Biliary tract neoplasms; Cisplatin; Jab1; Proliferation; Therapeutic target.

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / pharmacology
  • Biliary Tract Neoplasms / drug therapy
  • Biliary Tract Neoplasms / genetics
  • Biliary Tract Neoplasms / metabolism*
  • COP9 Signalosome Complex / antagonists & inhibitors
  • COP9 Signalosome Complex / genetics*
  • COP9 Signalosome Complex / metabolism*
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cisplatin / administration & dosage*
  • Cisplatin / pharmacology
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism
  • Drug Synergism
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Intracellular Signaling Peptides and Proteins / antagonists & inhibitors
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mice
  • PTEN Phosphohydrolase / chemistry
  • PTEN Phosphohydrolase / metabolism
  • Peptide Hydrolases / genetics*
  • Peptide Hydrolases / metabolism*
  • Protein Stability / drug effects
  • RNA, Small Interfering / administration & dosage
  • RNA, Small Interfering / pharmacology
  • Up-Regulation / drug effects
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents
  • CDKN1B protein, human
  • Intracellular Signaling Peptides and Proteins
  • RNA, Small Interfering
  • Cyclin-Dependent Kinase Inhibitor p27
  • PTEN Phosphohydrolase
  • PTEN protein, human
  • Peptide Hydrolases
  • COPS5 protein, human
  • COP9 Signalosome Complex
  • Cisplatin