Polymorphisms in the interleukin-4 receptor gene are associated with better survival in patients with glioblastoma

Michael E. Scheurer, E. Amirian, Yumei Cao, Mark R. Gilbert, Kenneth D. Aldape, David G. Kornguth, Randa El-Zein, Melissa L. Bondy

Research output: Contribution to journalArticle

39 Scopus citations

Abstract

Purpose: Previous literature provides some evidence that atopic diseases, IgE levels, and inflammatory gene polymorphisms may be associated with risk of glioblastoma. The purpose of this study was to investigate the effects of certain inflammatory gene single nucleotide polymorphisms (SNP) on patient survival. Malignant gliomas are the most common type of primary brain tumor in adults, however, few prognostic factors have been identified. Experimental Design: Using 694 incident adult glioma cases identified between 2001 and 2006 in Harris County, TX, we examined seven SNPs in the interleukin (IL)-4, IL-13, and IL-4 receptor (IL4R) genes. Cox proportional hazards regression was used to examine the association between the SNPs and overall and long-term survival, controlling for age at diagnosis, time between diagnosis and registration, extent of surgical resection, radiation therapy, and chemotherapy. Results: We found that among high-grade glioma cases, IL4R rs 1805016 (TT versus GT/GG) was significantly protective against mortality over time [ hazard ratios (HR), 0.59;95% confidence intervals (CI), 0.40-0.88]. The IL4R rs1805016 and rs1805015 TTgenotypes were both found to be significantly associated with survival beyond 1 year among patients with high-grade glioma (HR, 0.44;95% CI, 0.27-0.73 and HR, 0.63;95% CI, 0.44-0.91, respectively). Furthermore, the IL4R haplotype analysis showed that SNPs in the IL4R gene may be interacting to affect long-term survival among high-grade glioma cases. Conclusions: These findings indicate that polymorphisms in inflammation pathway genes may play an important role in glioma survival. Further research on the effects of these polymorphisms on glioma prognosis is warranted.

Original languageEnglish (US)
Pages (from-to)6640-6646
Number of pages7
JournalClinical Cancer Research
Volume14
Issue number20
DOIs
StatePublished - Oct 15 2008

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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