Vering A, Vockel A, Stegmüller M, Bender H G
Department of Gynecology, University Medical Center, Frankfurt am Main, Germany.
J Cancer Res Clin Oncol. 1993;119(7):415-20. doi: 10.1007/BF01218423.
The exact knowledge of hormone receptor status is critical for therapeutic strategies in hormone-dependent tumors. The influence of tamoxifen on estrogen receptor concentration has to be taken into account when evaluating results in tamoxifen-treated patients. We studied the receptor modulation of tumors xenotransplanted into nude mice (one breast and one endometrial carcinoma) after injection of 50 micrograms tamoxifen/mouse. To differentiate between unoccupied and occupied receptors, determinations were done by an enzyme immunoassay for the estrogen receptor under low- and high-salt extraction. With low-salt extraction we found a temporary decrease of the estrogen receptor concentration within the first hours after tamoxifen treatment. This decrease lasted for several days before recovery to pretreatment levels occurred. The hormone-receptor complexes, tightly bound to acceptor sites of the DNA, increased more than 15 times within 24 h. These values remained at increased levels for 2-7 days, after which a decrease to initial level was observed.
激素受体状态的确切信息对于激素依赖性肿瘤的治疗策略至关重要。在评估他莫昔芬治疗患者的结果时,必须考虑他莫昔芬对雌激素受体浓度的影响。我们研究了在每只小鼠注射50微克他莫昔芬后,异种移植到裸鼠体内的肿瘤(一个乳腺癌和一个子宫内膜癌)的受体调节情况。为了区分未占据和已占据的受体,通过酶免疫测定法在低盐和高盐提取条件下测定雌激素受体。低盐提取时,我们发现在他莫昔芬治疗后的最初几个小时内雌激素受体浓度暂时降低。这种降低持续数天,之后才恢复到治疗前水平。紧密结合于DNA受体位点的激素 - 受体复合物在24小时内增加了15倍以上。这些值在2 - 7天内保持升高水平,之后观察到降至初始水平。