Han Zihua, Zhang Lingzhi, Zhu Rujian, Luo Lifei, Zhu Min, Fan Lilong, Wang Guanfu
Luqiao Division of Affiliated Taizhou Hospital of Wenzhou Medical College Central Lab of Affiliated Taizhou Hospital of Wenzhou Medical College, Taizhou City, Zhejiang Province, China.
Medicine (Baltimore). 2017 Mar;96(13):e6473. doi: 10.1097/MD.0000000000006473.
The relationship of oestrogen receptor with benign prostatic hyperplasia (BPH) and prostate cancer (PC) is not clear at present. This study aimed to investigate the molecular mechanism underlying the occurrence and development of BPH and prostate.Two hundred forty-four PC cases, 260 BPH patients, and 222 healthy men were recruited from Han people in China, and the oestrogen receptor alpha (ESRα) gene polymorphism (rs2234693 [PvuII] and rs9340799 [XbaI]) on intron 1 was determined. The relationship of gene polymorphism with PC and BPH was evaluated with Logistic regression, and the linkage disequilibrium and haplotyping were assessed with SHEsis software.The risk for PC in BPH patients with PvuII C allele was higher (OR = 1.437, 95% CI: 1.110-1.859), but the differentiation degree of cancer cells was relatively better in PC patients with PvuII C allele (OR = 0.419, 95% CI: 0.285-0.616), and most of them are circumscribed (OR = 0.706, 95% CI: 0.485-1.02). There was significant linkage disequilibrium between PvuII and XbaI. The genotype TTAG not only induced BPH (OR = 6.260, 95% CI: 1.407-27.852), but increased the risk for PC (OR = 6.696, 95% CI: 1.504-29.801). However, the genotype TTAG in BPH patients had no relationship with the risk for PC (P > 0.05). Furthermore, men with haplotype TG were more likely to suffer PC (OR = 9.168, 95% CI: 2.393-35.119), but men with haplotype TA and enlarged prostate had a low risk for PC (OR = 0.708, 95% CI: 0.551-0.912).These results show the relationship between ESRα gene polymorphism and susceptibility to PC and BPH in Chinese men, and the ethnic and regional difference as well.
目前,雌激素受体与良性前列腺增生(BPH)和前列腺癌(PC)之间的关系尚不清楚。本研究旨在探讨BPH和前列腺发生发展的分子机制。从中国汉族人群中招募了244例PC患者、260例BPH患者和222名健康男性,检测了第1内含子上的雌激素受体α(ESRα)基因多态性(rs2234693 [PvuII]和rs9340799 [XbaI])。采用Logistic回归评估基因多态性与PC和BPH的关系,并用SHEsis软件评估连锁不平衡和单倍型。携带PvuII C等位基因的BPH患者患PC的风险较高(OR = 1.437,95%CI:1.110 - 1.859),但携带PvuII C等位基因的PC患者癌细胞分化程度相对较好(OR = 0.419,95%CI:0.285 - 0.616),且大多数为局限性(OR = 0.706,95%CI:0.485 - 1.02)。PvuII和XbaI之间存在显著的连锁不平衡。基因型TTAG不仅诱发BPH(OR = 6.260,95%CI:1.407 - 27.852),还增加患PC的风险(OR = 6.696,95%CI:1.504 - 29.801)。然而,BPH患者中的基因型TTAG与患PC的风险无关(P > 0.05)。此外,携带单倍型TG的男性更易患PC(OR = 9.168,95%CI:2.393 - 35.119),但携带单倍型TA且前列腺增大的男性患PC的风险较低(OR = 0.708,95%CI:0.551 - 0.912)。这些结果表明了ESRα基因多态性与中国男性PC和BPH易感性之间的关系,以及种族和地域差异。