HSPB1 polymorphisms might be associated with radiation-induced damage risk in lung cancer patients treated with radiotherapy

Tumour Biol. 2016 May;37(5):5743-9. doi: 10.1007/s13277-016-4959-4. Epub 2016 Feb 13.

Abstract

Several studies investigating the association between heat shock protein beta-1 (HSPB1) polymorphisms and radiation-induced damage in lung cancer patients administrated with radiotherapy have derived conflicting results. This meta-analysis aimed to assess the association between the HSPB1 genes' (rs2868370 and rs2868371) polymorphisms and the risk of radiation-induced damage in lung cancer patients. After an electronic literature search, four articles including six studies were found to be eligible for this meta-analysis. No association was observed between rs2868370 genotypes and radiation-induced damage risk. However, rs2868371 showed a statistically increased risk of radiation-induced damage under CC vs. CG/GG model (OR = 1.59, 95 % CI = 1.10-2.29). Subgroup analysis by ethnicity showed that the genotypes of rs2868371 were also associated with a significantly increased risk of radiation-induced damage in CC vs. CG/GG model (OR = 1.86, 95 % CI = 1.21-2.83) among mixed ethnicities which are mainly comprised of white people. When the data was stratified by organ-damaged, a significant association was only observed in the esophagus group (OR = 2.94, 95 % CI = 1.35-6.37, for CC vs. CG/GG model). In conclusion, the present study demonstrated that the rs2868371 genotypes of HSPB1 might be associated with radiation-induced esophagus damage risk, especially in Caucasians but not in the Asian population.

Keywords: Damage; HSPB1; Lung cancer; Polymorphism; Radiotherapy.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Asian People / genetics
  • Cytokines / metabolism
  • Esophagus / radiation effects
  • Genetic Predisposition to Disease
  • Genotype
  • Heat-Shock Proteins / genetics*
  • Heat-Shock Proteins / physiology
  • Humans
  • Lung / radiation effects
  • Lung Neoplasms / genetics*
  • Lung Neoplasms / radiotherapy
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / physiology
  • Polymorphism, Single Nucleotide*
  • Radiation Injuries / etiology
  • Radiation Injuries / genetics*
  • Radiotherapy / adverse effects*
  • Risk
  • White People / genetics

Substances

  • Cytokines
  • HSBP1 protein, human
  • Heat-Shock Proteins
  • Neoplasm Proteins