Human Reproduction, Vol. 17, No. 1, 150-156,
January 2002
© 2002 European Society of Human Reproduction and Embryology
Quantification of the expression level of the gene encoding the catalytic subunit of telomerase in testicular tissue specimens predicts successful sperm recovery
1 Department of Urology, Universitätsklinikum Benjamin Franklin, Freie Universität Berlin, Hindenburgdamm 30, 12200 Berlin and 2 Department of Andrology, University of Hamburg, Hamburg, Germany
BACKGROUND: The objective of the present study was to evaluate the quantitative detection of human telomerase reverse transcriptase (hTERT) mRNA as a new molecular diagnostic parameter in the work-up of testicular tissue specimens from patients presenting with non-obstructive azoospermia. M ETHODS: hTERT mRNA expression was quantified in 49 cryopreserved testicular tissue specimens by fluorescence real-time RTPCR in a LightCycler®. This was paralleled by conventional histological work-up in all tissue specimens and additional semithin sectioning preparation in cases with maturation arrest (n = 20) and Sertoli cell-only syndrome (SCOS; n = 12). RESULTS: The average normalized hTERT expression (NhTERT) was 136.1 ± 41.7 copies (mean ± standard deviation) in tissue specimens with presence of haploid germs cells, NhTERT = 48.2 ± 21.0 copies in those with maturation arrest and NhTERT = 2.7 ± 2.8 copies in those with SCOS. The discriminant analysis showed that detection of NhTERT was able correctly to classify 89.0% of the investigated tissue specimens. CONCLUSIONS: Our results demonstrate that quantitative detection of hTERT mRNA expression in testicular tissue enables a moleculardiagnostic subclassification of spermatogenesis disorders. Quantitative detection of hTERT in testicular biopsies is thus well suited for predicting successful sperm recovery in patients with azoospermia and is a useful molecular diagnostic parameter for supplementing the histopathological evaluation.
Key words: fertility/human telomerase reverse transcriptase/human telomerase RNA/spermatogenesis
3 To whom correspondence should be addressed: E-mail: schrader{at}medizin.fu-berlin.de
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