Meta- and Pooled Analysis of GSTP1 Polymorphism and Lung Cancer: A HuGEGSEC Review

Lung cancer is the most common cancer worldwide. Polymorphisms in genes associated with carcinogen metabolism may modulate risk of disease. Glutathione S-transferase pi (GSTP1) detoxifies polycyclic aromatic hydrocarbons found in cigarette smoke and is the most highly expressed glutathione S-transferase in lung tissue. A polymorphism in the GSTP1 gene, an A-to-G transition in exon 5 (Ile105Val, 313A / 313G), results in lower activity among individuals who carry the valine allele. The authors present a meta- and a pooled analysis of casecontrol studies that examined the association between this polymorphism in GSTP1 and lung cancer risk (27 studies, 8,322 cases and 8,844 controls and 15 studies, 4,282 cases and 5,032 controls, respectively). Overall, the meta-analysis found no significant association between lung cancer risk and the GSTP1 exon 5 polymorphism. In the pooled analysis, there was an overall association (odds ratio ¼ 1.11, 95% confidence interval: 1.03, 1.21) between lung cancer and carriage of the GSTP1 Val/Val or Ile/Val genotype compared with those carrying the Ile/ Ile genotype. Increased risk varied by histologic type in Asians. There appears to be evidence for interaction between amount of smoking, the GSTP1 exon 5 polymorphism, and risk of lung cancer in whites. Michele L. Cote, Wei Chen, Daryn W. Smith, Simone Benhamou, Christine Bouchardy, Dorota Butkiewicz, Kwun M. Fong, Manuel Gene´ , Ari Hirvonen, Chikako Kiyohara, Jill E. Larsen, Pinpin Lin, Ole Raaschou-Nielsen, Andrew C. Povey, Edyta Reszka, Angela Risch, Joachim Schneider, Ann G. Schwartz, Mette Sorensen, Jordi To-Figueras, Shinkan Tokudome, Yuepu Pu, Ping Yang, Angela S. Wenzlaff, Harriet Wikman, and Emanuela Taiol