HPC2 variants and screen-detected prostate cancer

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Abstract

Two studies have reported significant associations between susceptibility to prostate cancer and two common missense variants of the HPC2/ELAC2 gene, with estimated relative risks in the range of two- to threefold. We investigated whether these polymorphisms could be informative in the prediction of the presence of prostate cancer in men undergoing prostatic biopsy for the evaluation of an elevated serum-PSA level (≥4.0 ng/ml). We genotyped 944 men who underwent a prostate biopsy at our institution, as well as a control population of 922 healthy, unselected women from the same population. The prevalence of the HPC2 Ala541Thr allele was similar in men with prostate cancer (6.3%), men with other prostatic conditions (6.8%), and healthy women (6.3%) (P = .83). We conclude that HPC2 genotyping is unlikely to be a useful adjunct to PSA in the prediction of the presence of biopsy-detected prostate cancer in asymptomatic men.

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Vesprini, D., Nam, R. K., Trachtenberg, J., Jewett, M. A. S., Tavtigian, S. V., Emami, M., … Narod, S. A. (2001). HPC2 variants and screen-detected prostate cancer. American Journal of Human Genetics, 68(4), 912–917. https://doi.org/10.1086/319502

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