Wyatt Kara D, Sakamoto Kaori, Watford Wendy T
Department of Infectious Diseases, University of Georgia, USA.
Department of Pathology, University of Georgia, USA.
Lab Anim. 2022 Jun;56(3):297-303. doi: 10.1177/00236772211042968. Epub 2021 Sep 22.
Tamoxifen is commonly used as a cancer treatment in humans and for inducing genetic alterations using Cre-lox mouse models in the research setting. However, the extent of tamoxifen off-target effects in animal research is underappreciated. Here, we report significant changes in cellular infiltration in Cre-recombinase-negative mice treated with tamoxifen intraperitoneally. These changes were noted in the lungs, which were characterized by the presence of alveolitis, vasculitis, and pleuritis. Despite significant immunological changes in response to tamoxifen treatment, clinical symptoms were not observed. This study provides a cautionary note that tamoxifen treatment alone leads to histologic alterations that may obscure research interpretations and further highlights the need for the development of alternative mouse models for inducible Cre-mediated deletion.
他莫昔芬常用于人类癌症治疗以及在研究环境中使用Cre-lox小鼠模型诱导基因改变。然而,在动物研究中他莫昔芬脱靶效应的程度尚未得到充分认识。在此,我们报告了经腹腔注射他莫昔芬处理的Cre重组酶阴性小鼠细胞浸润的显著变化。这些变化在肺部被观察到,其特征为存在肺泡炎、血管炎和胸膜炎。尽管对他莫昔芬治疗有显著的免疫反应变化,但未观察到临床症状。本研究警示单独使用他莫昔芬治疗会导致组织学改变,这可能会模糊研究解读,并进一步凸显了开发用于诱导性Cre介导缺失的替代小鼠模型的必要性。