RAGE genetic polymorphisms are associated with risk, chemotherapy response and prognosis in patients with advanced NSCLC

PLoS One. 2012;7(10):e43734. doi: 10.1371/journal.pone.0043734. Epub 2012 Oct 5.

Abstract

Aim: To explore the association between genetic polymorphisms of the receptor for advanced glycation end-products (RAGE) and susceptibility, chemotherapy response rate and prognosis of non-small cell lung cancer (NSCLC).

Method: This is a prospective study in which 562 patients with NSCLC and 764 healthy controls were enrolled. Three RAGE genetic polymorphisms, namely, -429T/C, -374T/A and 82G/S were genotyped. Platinum-based chemotherapy was given to 432 subjects with advanced inoperable NSCLC and their responses to chemotherapy were evaluated.

Results: All the polymorphic genotypes of RAGE polymorphisms were associated with susceptibility for NSCLC. Only the 82G/S polymorphisms denoted a significant difference between responders and non-responders to chemotherapy. The 82SS genotype and 82S allele distribution not only increased the NSCLC risk, but also was associated with a lower chemotherapy response rate and poor prognosis, indicated by overall survival and progression free survival.

Conclusion: The 82G/S genetic polymorphism of RAGE gene might be used as a genetic marker to screen for patients sensitive to thermotherapy and to predict the prognosis of NSCLC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Drug Resistance, Neoplasm
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / genetics*
  • Male
  • Middle Aged
  • Organoplatinum Compounds / therapeutic use*
  • Polymorphism, Single Nucleotide
  • Prognosis
  • Prospective Studies
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic / genetics*

Substances

  • Organoplatinum Compounds
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic

Grants and funding

The study is supported by a grant from Huzhou science and technology development project (HZ 2006–12). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.