Fibroblast growth factor receptor 2 gene amplification status and its clinicopathologic significance in gastric

Eun-Jung Jung1, Eun-Ji Jung, Sun Young Min

  • 1Department of Pathology, Seoul National University College of Medicine, Seoul 110-799, Republic of Korea.

Human Pathology
|March 24, 2012
PubMed

Insights

Fibroblast growth factor receptor 2 (FGFR2) amplification occurs in 4.5% of gastric cancers. This amplification is linked to advanced disease and poorer survival, suggesting FGFR2 inhibitors may benefit specific patient subsets.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Fibroblast growth factor receptor 2 (FGFR2) is a receptor tyrosine kinase implicated in various cancers.
  • FGFR2 gene amplification or mutation is observed in gastric carcinoma, a leading cause of cancer death.
  • Targeted therapies against FGFR2 show promise in inhibiting tumor progression.

Purpose of the Study:

  • To evaluate the frequency of FGFR2 gene amplification in gastric carcinoma.
  • To investigate the association between FGFR2 amplification and clinicopathologic parameters.
  • To determine the prognostic significance of FGFR2 amplification in gastric cancer patients.

Main Methods:

  • Fluorescence in situ hybridization (FISH) was used to assess FGFR2 amplification in 313 gastric carcinoma tissues.
  • Quantitative real-time polymerase chain reaction (qPCR) validated FISH results.
  • Clinicopathologic parameters and survival data were analyzed in relation to FGFR2 amplification status.

Main Results:

  • FGFR2 amplification was detected in 14 (4.5%) of 313 gastric carcinoma cases.
  • FGFR2 amplification correlated significantly with higher pT stage, higher pN stage, and distant metastasis.
  • Univariate analysis revealed a significant association between FGFR2 amplification and poorer cancer-specific survival.

Conclusions:

  • FGFR2 amplification in gastric carcinoma is associated with advanced disease and unfavorable prognosis.
  • Identifying FGFR2 amplification status may help select patients for targeted FGFR2 inhibitor therapy.
  • This finding supports the potential of FGFR2-targeted agents for a subset of gastric cancer patients.