| It has been hypothesized that several genes involved in androgen metabolism may be associated with prostate cancer risk. Among these, type III 17β-HSD converts androstenedione to testosterone primarily in the testis. In this study, we assessed the association between three amino acid substitutions in the HSD17B3 gene and prostate cancer risk in a case-cohort study within the Los Angeles/Hawaii Multiethnic Cohort Study (MEC). We did not find any statistically significant association between SNPs in the gene and prostate cancer risk. However, among Japanese-American men, compared to those with two G alleles in G289S, people with one or more S allele had an OR of 1.97 (95% CI = 1.05–3.71). In general the HSD17B3 variants are not good biomarkers of susceptibility to prostate cancer. Our finding in the Japanese-American group suggests that the effects of these variants might be more important in Asian populations. |