GGN repeat length and GGN/CAG haplotype variations in the androgen receptor gene and prostate cancer risk in south Indian men

Autor: K. N. Vishwanathan, Kumarasamy Thangaraj, Sunil Shroff, Perumal Venkatesan, Singh Rajender, V. Vettriselvi, Solomon F. D. Paul, K. Vijayalakshmi
Rok vydání: 2006
Předmět:
Zdroj: Journal of Human Genetics. 51:998-1005
ISSN: 1435-232X
1434-5161
Popis: The ethnic variation in the GGN and CAG microsatellites of the androgen receptor (AR) gene suggests their role in the substantial racial difference in prostate cancer risk. Hence, we performed a case-control study to assess whether GGN repeats independently or in combination with CAG repeats were associated with prostate cancer risk in South Indian men. The repeat lengths of the AR gene determined by Gene scan analysis, revealed that men with GGN repeatsor=21 had no significant risk compared to those with21 repeats (OR 0.91 at 95% CI-0.52-1.58). However, when CAG repeats of our earlier study was combined with the GGN repeat data, the cases exhibited significantly higher frequency of the haplotypes CAGor=19/GGNor=21 (OR-5.2 at 95% CI-2.17-12.48, P0.001) and CAGor=19/GGN21(OR-6.9 at 95%CI-2.85-17.01, P0.001) compared to the controls. No significant association was observed between GGN repeats and prostate-specific antigen levels and the age at diagnosis. Although a trend of short GGN repeats length in high-grade was observed, it was not significant (P = 0.09). Overall, our data reveals that specific GGN/CAG haplotypes (CAGor=19/GGNor=21 and CAGor=19/GGN21) of AR gene increase the risk of prostate cancer and thus could serve as susceptibility marker for prostate cancer in South Indian men.
Databáze: OpenAIRE