Tamoxifen administration to mice

Jonathan Whitfield, Trevor Littlewood, Laura Soucek

Research output: Contribution to journalArticleResearchpeer-review

10 Citations (Scopus)

Abstract

© 2015 Cold Spring Harbor Laboratory Press. The strategy of fusing a protein of interest to a hormone-binding domain (HBD) of a steroid hormone receptor allows fine control of the activity of the fused protein. Such fusion proteins are inactive in the absence of ligand, because they are complexed with a variety of intracellular polypeptides. Upon ligand binding, the receptor is released from its inhibitory complex and the fusion protein becomes functional. In the murine estrogen receptor (ER) fusion system, proteins are fused to the HBD of the ER. The system relies on the use of a mutant ER known as ERTAM. Compared to the wild-type HBD, ERTAM has 1000-fold lower affinity for estrogen, yet remains responsive to activation by the synthetic steroid 4- hydroxytamoxifen (4-OHT). Because 4-OHT is expensive, animals can be treated with the cheaper precursor tamoxifen, which is converted into 4-OHT by a liver enzyme. Here we present an overview of the methods used to deliver tamoxifen to mice. The most used method is intraperitoneal injection, because the amount of administered compound can be better controlled, but delivery by oral gavage is also possible. For short-term and immediate-effect studies or when conversion of tamoxifen by the liver is to be avoided, 4-OHT can be used directly.
Original languageEnglish
Pages (from-to)269-271
JournalCold Spring Harbor Protocols
Volume2015
Issue number3
DOIs
Publication statusPublished - 1 Jan 2015

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