Murphy C, Fotsis T, Pantzar P, Adlercreutz H, Martin F
Department of Pharmacology, University College Dublin, Republic of Ireland.
J Steroid Biochem. 1987 Dec;28(6):609-18. doi: 10.1016/0022-4731(87)90387-6.
Tamoxifen, 4-hydroxytamoxifen and desmethyltamoxifen levels were measured in cytosolic and 0.5 M KCl extracted nuclear fractions from a small series of breast tumours from tamoxifen treated patients by gas chromatography-mass spectrometry (GC-MS) using selected ion monitoring (SIM). Tamoxifen and desmethyltamoxifen were the most abundant metabolites. There was a small increment in the relative abundance of 4-hydroxytamoxifen in the nuclear extract over cytosol relative to both tamoxifen and desmethyltamoxifen. Further, there was a selective retention of tamoxifen relative to desmethyltamoxifen in the nuclear extract relative to the cytosol. It is concluded that all three compounds could potentially contribute to estrogen receptor mediated antiestrogenic effects in this target tissue.
通过气相色谱 - 质谱联用(GC-MS)并采用选择离子监测(SIM)技术,测定了一小系列接受他莫昔芬治疗的乳腺癌患者肿瘤组织的胞质和0.5M KCl提取的核级分中的他莫昔芬、4 - 羟基他莫昔芬和去甲基他莫昔芬水平。他莫昔芬和去甲基他莫昔芬是最丰富的代谢产物。相对于他莫昔芬和去甲基他莫昔芬,核提取物中4 - 羟基他莫昔芬相对于胞质的相对丰度有小幅增加。此外,相对于胞质,核提取物中他莫昔芬相对于去甲基他莫昔芬有选择性保留。结论是,这三种化合物都可能在该靶组织中对雌激素受体介导的抗雌激素作用有贡献。