The incidence rate of testicular cancer has been steadily increasing d
uring the last 50 years, and only cryptorchidism, i.e. undescended tes
tes, has been identified as an important risk factor. An interplay bet
ween changing environmental factors and genetic susceptibility e.g. in
foreign compound metabolizing enzymes, may have important influences
on the risk. The aim of this study was to investigate if glutathione S
-transferase mu (GST mu) deficiency, which in previous studies has bee
n associated with malignant melanoma and cancers of the lung and bladd
er, is a risk factor of testicular cancer. Three hundred and seventy-e
ight men participated (80 seminomas, 104 non-seminomas and 194 control
s) in a population-based case-control study. The phenotype of GST mu w
as determined in 366 men by ELISA, the genotype was determined in 324
men by polymerase chain reaction. The concordance between geno- and ph
enotype tvas 94.4%. The odds ratio of having the GST mu negative pheno
type and testicular cancer was 1.08, (0.72-1.64; 95% confidence interv
al (CI)), and the odds ratio of having the GSTM1 null genotype and tes
ticular cancer was 1.10; CI95% (0.71-1.70). This study provides no evi
dence of an association between phenotypically determined GST mu defic
iency or GSTM1 null genotype and testicular cancer. The narrow confide
nce intervals rule out GST mu as a major single risk factor for testic
ular cancer.