Gastrin inhibits gastric cancer progression through activating the ERK-P65-miR23a/27a/24 axis

J Exp Clin Cancer Res. 2018 Jun 4;37(1):115. doi: 10.1186/s13046-018-0782-7.

Abstract

Background: To test the hypothesis that activated extracellular signal-regulated kinase (ERK) regulates P65-miR23a/27a/24 axis in gastric cancer (GC) and the ERK-P65-miR23a/27a/24 axis plays an important role in the development of GC, and to evaluate the role of gastrin in GC progression and ERK-P65-miR23a/27a/24 axis.

Methods: The component levels of the ERK-P65-miR23a/27a/24 axis in four fresh GC tissues, 101 paraffin-embedded GC tissues and four GC cell lines were determined by Western blotting, immunohistochemistry (IHC) or qRT-PCR. The effects of gastrin on GC were first evaluated by measuring gastrin serum levels in 30 healthy and 70 GC patients and performing a correlation analysis between gastrin levels and survival time in 27 GC patients after eight years of follow-up, then evaluated on GC cell lines, GC cell xenograft models, and patient-derived xenografts (PDX) mouse models. The roles of ERK-P65-miR23a/27a/24 axis in GC progression and in the effects of gastrin on GC were examined.

Results: ERK- P65-miR23a/27a/24 axis was proved to be present in GC cells. The levels of components of ERK-P65-miR23a/27a/24 axis were decreased in GC tissue samples and PGC cells. The decreased levels of components of ERK-P65-miR23a/27a/24 axis were associated with poor prognosis of GC, and ERK-P65-miR23a/27a/24 axis played a suppressive role in GC progression. Low blood gastrin was correlated with poor prognosis of the GC patients and decreased expression of p-ERK and p-P65 in GC tissues. Gastrin inhibited proliferation of poorly-differentiated GC (PGC) cells through activating the ERK-P65-miR23a/27a/24 axis. Gastrin inhibited GC growth and enhanced the suppression of GC by cisplatin in mice or PGC cell culture models through activating the ERK-P65-miR23a/27a/24 axis or its components.

Conclusions: ERK-P65-miR23a/27a/24 axis is down-regulated, leading to excess GC growth and poor prognosis of GC. Low gastrin promoted excess GC growth and contributed to the poor prognosis of the GC patients by down-regulating ERK-P65-miR23a/27a/24 axis. Gastrin inhibits gastric cancer growth through activating the ERK-P65-miR23a/27a/24 axis.

Keywords: ERK; Gastric cancer; Gastrin; P65; miR23a/27a/24 cluster.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cisplatin / pharmacology
  • Disease Models, Animal
  • Disease Progression
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Female
  • Gastrins / metabolism*
  • Gene Expression
  • Gene Expression Regulation, Neoplastic*
  • Genes, Reporter
  • Heterografts
  • Humans
  • Mice
  • MicroRNAs / genetics*
  • RNA Interference
  • Signal Transduction
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / metabolism*
  • Stomach Neoplasms / pathology
  • Transcription Factor RelA / metabolism*

Substances

  • Gastrins
  • MIRN23a microRNA, human
  • MIRN24 microRNA, human
  • MicroRNAs
  • Transcription Factor RelA
  • Extracellular Signal-Regulated MAP Kinases
  • Cisplatin