Edwards J, Krishna N S, Grigor K M, Bartlett J M S
Endocrine Cancer Group, Surgical and Translational research section, Division of Cancer Sciences and Molecular Pathology, Glasgow Royal Infirmary, Glasgow G31 2ER, Scotland.
Br J Cancer. 2003 Aug 4;89(3):552-6. doi: 10.1038/sj.bjc.6601127.
This study examined androgen receptor (AR) gene amplification and protein expression in 102 matched paired hormone sensitive and resistant tumours from 51 patients. AR gene amplification and X chromosome copy number were assessed by fluorescent in situ hybridisation, and protein expression was assessed by immunohistochemistry. All tumours were stained for PSA protein expression. Significantly more tumours exhibited AR amplification following the development of hormone resistance (20%, 10 out of 49) compared to matched hormone-sensitive tumours from the same patient (2%, one out of 48) (P=0.0085). The level of AR expression was significantly higher in hormone-resistant tumours compared to matched hormone-sensitive tumours from the same patient (130, interquartile range, 55-167 vs 94.5 interquartile range, 55-120, P=0.019). AR expression levels in hormone-resistant tumours with and without AR amplification were not significantly different. However, an increase in AR expression was seen with the development of AR amplification in paired tumours. The rate of AR gene amplification and/or an increase in AR protein expression during androgen resistant is too low to wholly explain the development of androgen resistance. Alternative mechanisms for modulating the function of the AR, or other signalling pathways, must be considered as key factors in the development of hormone-resistant prostate.
本研究检测了来自51例患者的102对配对的激素敏感和耐药肿瘤中雄激素受体(AR)基因扩增及蛋白表达情况。通过荧光原位杂交评估AR基因扩增和X染色体拷贝数,通过免疫组织化学评估蛋白表达。所有肿瘤均进行前列腺特异性抗原(PSA)蛋白表达染色。与同一患者配对的激素敏感肿瘤相比(2%,48例中的1例),激素耐药肿瘤发生后出现AR扩增的肿瘤显著更多(20%,49例中的10例)(P=0.0085)。与同一患者配对的激素敏感肿瘤相比,激素耐药肿瘤中AR表达水平显著更高(四分位间距为55 - 167时为130,四分位间距为55 - 120时为94.5,P=0.019)。有和没有AR扩增的激素耐药肿瘤中AR表达水平无显著差异。然而,在配对肿瘤中,随着AR扩增的出现,AR表达增加。雄激素抵抗期间AR基因扩增率和/或AR蛋白表达增加过低,无法完全解释雄激素抵抗的发生。调节AR功能或其他信号通路的替代机制必须被视为激素抵抗性前列腺癌发生的关键因素。