Replication study in Chinese population and meta-analysis supports association of the 5p15.33 locus with lung cancer

PLoS One. 2013 Apr 30;8(4):e62485. doi: 10.1371/journal.pone.0062485. Print 2013.

Abstract

Background: Common genetic polymorphisms on chromosome 5p15.33, including rs401681 in cleft lip and palate transmembrane 1-like gene (CLPTM1L), have been implicated in susceptibility to lung cancer through genome-wide association studies (GWAS); however, subsequent replication studies yielded controversial results.

Methodology and findings: A hospital-based case-control study in a Chinese population was conducted to replicate the association, and then a meta-analysis combining our non-overlapping new data and previously published data was performed to clearly discern the real effect of lung cancer susceptibility. In our study with 611 cases and 1062 controls, the minor allele T carrier (TT plus CT) group conferred an OR of 0.801 (95% CI = 0.654-0.981) under the dominant model. The meta-analysis comprising 9111 cases and 11424 controls further confirmed the significant association in the dominant model (OR = 0.842, 95% CI = 0.795-0.891). By stratified analysis, we revealed that ethnicity and study design might constitute the source of between-study heterogeneity. Besides, the sensitivity and cumulative analyses indicated the high stability of the results.

Conclusion: The results from our case-control study and meta-analysis provide convincing evidence that rs401681 is significantly associated with lung cancer risk.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Alleles
  • Carcinoma, Non-Small-Cell Lung / ethnology
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Case-Control Studies
  • China / epidemiology
  • Chromosomes, Human, Pair 5
  • Female
  • Gene Frequency
  • Genetic Loci*
  • Genetic Predisposition to Disease*
  • Genome-Wide Association Study
  • Humans
  • Lung Neoplasms / ethnology
  • Lung Neoplasms / genetics*
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Models, Genetic
  • Neoplasm Proteins / genetics*
  • Polymorphism, Single Nucleotide*
  • Risk Factors

Substances

  • CLPTM1L protein, human
  • Membrane Proteins
  • Neoplasm Proteins

Grants and funding

This work was supported by the Program for New Century Excellent Talents in University [NCET-10-0388 to MX]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.