Mononen Nina, Ikonen Tarja, Autio Ville, Rökman Annika, Matikainen Mika P, Tammela Teuvo L J, Kallioniemi Olli-P, Koivisto Pasi A, Schleutker Johanna
Laboratory of Cancer Genetics, Institute of Medical Technology, University of Tampere and Tampere University Hospital, Lenkkeilijankatu 6, 33520 Tampere, Finland.
Hum Genet. 2002 Aug;111(2):166-71. doi: 10.1007/s00439-002-0776-5. Epub 2002 Jul 3.
Recent studies have suggested that polymorphisms of the androgen receptor gene ( AR) may influence the risk of prostate cancer (PC) development and progression. Here, we analyzed the length of the CAG repeat of the AR gene in 1363 individuals, including patients with PC, benign prostate hyperplasia (BPH), and population controls. There was a tendency for short CAG repeats to be associated with PC. The Odds Ratio (OR) for PC was 1.47 ( P=0.05) when individuals with short CAG repeats (</=18) were compared with those having long repeats (>18). CAG repeat length was not significantly associated with family history, disease stage, grade, age at diagnosis, prostate-specific antigen (PSA) level at diagnosis, or prognosis of the patients. Unexpectedly, short CAG repeats were significantly less common in patients with BPH compared with controls (OR=0.47, P=0.03). Our results suggest that the CAG polymorphism of the AR gene is unlikely to have a major role in the development or progression of PC in the Finnish population. The association of CAG repeats with the risk of BPH warrants further study.
近期研究表明,雄激素受体基因(AR)的多态性可能会影响前列腺癌(PC)发生和进展的风险。在此,我们分析了1363名个体中AR基因CAG重复序列的长度,这些个体包括前列腺癌患者、良性前列腺增生(BPH)患者以及人群对照。CAG重复序列短的个体有与前列腺癌相关的趋势。当将CAG重复序列短(≤18)的个体与重复序列长(>18)的个体进行比较时,前列腺癌的优势比(OR)为1.47(P = 0.05)。CAG重复序列长度与患者的家族史、疾病分期、分级、诊断时年龄、诊断时前列腺特异性抗原(PSA)水平或预后均无显著相关性。出乎意料的是,与对照组相比,BPH患者中CAG重复序列短的情况明显较少见(OR = 0.47,P = 0.03)。我们的结果表明,在芬兰人群中,AR基因的CAG多态性不太可能在前列腺癌的发生或进展中起主要作用。CAG重复序列与BPH风险之间的关联值得进一步研究。