Charoenchokthavee Wanaporn, Ayudhya Duangchit Panomvana Na, Sriuranpong Virote, Areepium Nutthada
Department of Pharmacy Practice, Faculty of Pharmaceutical Science, Chulalongkorn University, Bangkok, Thailand E-mail :
Asian Pac J Cancer Prev. 2016;17(4):1851-5. doi: 10.7314/apjcp.2016.17.4.1851.
Tamoxifen is a pharmacological estrogen inhibitor that binds to the estrogen receptor (ER) in breast cells. However, it shows an estrogenic effect in other organs, which causes adverse drug reactions (ADRs). The sulfotransferase 1A1 (SULT1A1) enzyme encoded by the SULT1A1 gene is involved in estrogen metabolism. Previous research has suggested that the SULT1A1 copy number is linked with the plasma estradiol (E2) concentration. Here, a total of 34 premenopausal breast cancer patients, selected from the Thai Tamoxifen (TTAM) Project, were screened for their SULT1A1 copy number, plasma E2 concentration and ADRs. The mean age was 44.3±11.1 years, and they were subtyped as ER+/ progesterone receptor (PR) + (28 patients), ER+/ PR- (5 patients) and ER-/PR- (1 patient). Three patients reported ADRs, which were irregular menstruation (2 patients) and vaginal discharge (1 patient). Most (33) patients had two SULT1A1 copies, with one patient having three copies. The median plasma E2 concentration was 1,575.6 (IQR 865.4) pg/ml. Patients with ADRs had significantly higher plasma E2 concentrations than those patients without ADRs (p = 0.014). The plasma E2 concentration was numerically higher in the patient with three SULT1A1 copies, but this lacked statistical significance.
他莫昔芬是一种药理雌激素抑制剂,可与乳腺细胞中的雌激素受体(ER)结合。然而,它在其他器官中表现出雌激素样作用,从而导致药物不良反应(ADR)。由SULT1A1基因编码的磺基转移酶1A1(SULT1A1)参与雌激素代谢。先前的研究表明,SULT1A1拷贝数与血浆雌二醇(E2)浓度有关。在此,从泰国他莫昔芬(TTAM)项目中选取了34名绝经前乳腺癌患者,对其SULT1A1拷贝数、血浆E2浓度和ADR进行了筛查。平均年龄为44.3±11.1岁,其亚型为ER+/孕激素受体(PR)+(28例患者)、ER+/PR-(5例患者)和ER-/PR-(1例患者)。3例患者报告了ADR,分别为月经不调(2例患者)和阴道分泌物异常(1例患者)。大多数(33例)患者有两个SULT1A1拷贝,1例患者有三个拷贝。血浆E2浓度中位数为1575.6(四分位间距865.4)pg/ml。发生ADR的患者血浆E2浓度显著高于未发生ADR的患者(p = 0.014)。有三个SULT1A1拷贝的患者血浆E2浓度在数值上更高,但缺乏统计学意义。