Department of Nutritional Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Oklahoma Center for Geroscience, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Endocrinology. 2021 Sep 1;162(9). doi: 10.1210/endocr/bqab126.
The selective estrogen receptor (ER) modulator tamoxifen is frequently used in preclinical studies to induce Cre recombinase and generate conditional transgenic mice. In addition, it is often prescribed to treat ER-positive breast cancer, which is diagnosed in approximately 150 000 people each year. In mice, protocols to activate Cre-ER transgenes require tamoxifen administration by several methods, including oral gavage, IP injection, or intragastric injection, spanning a wide range of doses to achieve transgene induction. As a result, the reported metabolic effects of tamoxifen treatment are not always consistent with anecdotal reports from breast cancer patients, or with expected outcomes based on the overall metabolically protective role of estrogen. A greater awareness of tamoxifen's adverse metabolic effects is critical to designing studies with appropriate controls, especially those investigations focused on metabolic outcomes.
选择性雌激素受体 (ER) 调节剂他莫昔芬常用于临床前研究中诱导 Cre 重组酶并产生条件性转基因小鼠。此外,它通常被用于治疗雌激素受体阳性乳腺癌,每年约有 150000 人被诊断出患有这种癌症。在小鼠中,激活 Cre-ER 转基因的方案需要通过多种方法给予他莫昔芬,包括口服灌胃、腹腔注射或胃内注射,剂量范围很广,以实现转基因的诱导。因此,他莫昔芬治疗的代谢效应的报道并不总是与乳腺癌患者的传闻报告一致,也与雌激素的整体代谢保护作用所预期的结果不一致。提高对他莫昔芬不良代谢作用的认识对于设计具有适当对照的研究至关重要,特别是那些关注代谢结果的研究。