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No association of the NFKB1 insertion/deletion promoter polymorphism with survival in patients with gastric cancer

  • Jong Gwang Kim
  • , Sang Kyun Sohn
  • , Yee Soo Chae
  • , Joon Ho Moon
  • , Shi Nae Kim
  • , Byung Woog Kang
  • , Gab Chul Kim
  • , Myung Hoon Lee
  • , Seong Woo Jeon
  • , Ho Young Chung
  • , Wansik Yu
  • Kyungpook National University

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Objective: The present study analyzed the functional insertion/deletion polymorphism in the promoter region of NFKB1 gene and their impact on the prognosis for patients with gastric adenocarcinoma. Methods: Four hundred and seventy two consecutive patients with curatively resected gastric adenocarcinoma were enrolled in the present study. The genomic DNA was extracted from paraffin-embedded tissue and the -94 insertion/deletion ATTG polymorphism of NFKB1 determined using a polymerase chain reaction-restriction fragment length polymorphism assay. Results: The NFKB1 promoter gene polymorphism was successfully amplified in 97.8% of the cases. There were no sexual differences in relation to the genotype and allele. No correlation was observed between the frequency of the genotype or allele and the T, N or M stage. The multivariate survival analysis showed no association between the NFKB1 -94 insertion/deletion promoter polymorphism and the disease-free survival or overall survival of the patients with gastric cancer. Conclusions: The functional NFKB1 promoter polymorphism was not found to be a prognostic marker for Korean patients with surgically resected gastric adenocarcinoma.

Original languageEnglish
Pages (from-to)497-501
Number of pages5
JournalJapanese Journal of Clinical Oncology
Volume39
Issue number8
DOIs
StatePublished - 2009

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Gastric cancer
  • NFKB1
  • Polymorphism
  • Prognosis

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