In Vivo Performance and Properties of Tamoxifen Metabolites for CreERT2 Control
Language English Country United States Media electronic-ecollection
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27077909
PubMed Central
PMC4831813
DOI
10.1371/journal.pone.0152989
PII: PONE-D-15-53789
Knihovny.cz E-resources
- MeSH
- Cell Line MeSH
- Time Factors MeSH
- Zebrafish MeSH
- Integrases genetics MeSH
- Humans MeSH
- Receptors, Estrogen chemistry genetics MeSH
- Recombination, Genetic drug effects MeSH
- Recombinant Fusion Proteins chemistry genetics MeSH
- Drug Stability MeSH
- Stereoisomerism MeSH
- Tamoxifen analogs & derivatives chemistry metabolism pharmacology MeSH
- Protein Structure, Tertiary MeSH
- Hot Temperature MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 4-hydroxy-N-desmethyltamoxifen MeSH Browser
- Cre recombinase MeSH Browser
- Integrases MeSH
- Receptors, Estrogen MeSH
- Recombinant Fusion Proteins MeSH
- Tamoxifen MeSH
Mutant Estrogen Receptor (ERT2) ligand-binding domain fusions with Cre recombinase are a key tool for spatio-temporally controlled genetic recombination with the Cre/lox system. CreERT2 is efficiently activated in a concentration-dependent manner by the Tamoxifen metabolite trans-4-OH-Tamoxifen (trans-4-OHT). Reproducible and efficient Cre/lox experimentation is hindered by the gradual loss of CreERT2 induction potency upon prolonged storage of dissolved trans-4-OHT, which potentially results from gradual trans-to-cis isomerization or degradation. Here, we combined zebrafish CreERT2 recombination experiments and cell culture assays to document the gradual activity loss of trans-4-OHT and describe the alternative Tamoxifen metabolite Endoxifen as more stable alternative compound. Endoxifen retains potent activation upon prolonged storage (3 months), yet consistently induces half the ERT2 domain fusion activity compared to fresh trans-4-OHT. Using 1H-NMR analysis, we reveal that trans-4-OHT isomerization is undetectable upon prolonged storage in either DMSO or Ethanol, ruling out isomer transformation as cause for the gradual loss of trans-4-OHT activity. We further establish that both trans-4-OHT and Endoxifen are insensitive to light exposure under regular laboratory handling conditions. We attribute the gradual loss of trans-4-OHT potency to precipitation over time, and show that heating of aged trans-4-OHT aliquots reinstates their CreERT2 induction potential. Our data establish Endoxifen as potent and reproducible complementary compound to 4-OHT to control ERT2 domain fusion proteins in vivo, and provide a framework for efficient chemically controlled recombination experiments.
CZ OPENSCREEN Institute of Molecular Genetics of the ASCR v v i Prague Czech Republic
Department of Chemistry University of Zürich Zürich Switzerland
Institute of Molecular and Cell Biology A*STAR Biopolis Drive Singapore Singapore
Institute of Molecular Life Sciences University of Zürich Zürich Switzerland
See more in PubMed
Feil R, Wagner J, Metzger D, Chambon P. Regulation of Cre recombinase activity by mutated estrogen receptor ligand-binding domains. Biochem Biophys Res Commun. 1997;237: 752–757. Available: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=9299439 PubMed
Feil R, Brocard J, Mascrez B, LeMeur M, Metzger D, Chambon P. Ligand-activated site-specific recombination in mice. Proc Natl Acad Sci U S A. 1996;93: 10887–10890. Available: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=8855277 PubMed PMC
Sinha DK, Neveu P, Gagey N, Aujard I, Benbrahim-Bouzidi C, Le Saux T, et al. Photocontrol of protein activity in cultured cells and zebrafish with one- and two-photon illumination. Chembiochem. 2010;11: 653–63. 10.1002/cbic.201000008 PubMed DOI
Wakeling AE, Dukes M, Bowler J. A potent specific pure antiestrogen with clinical potential. Cancer Res. 1991;51: 3867–73. Available: http://www.ncbi.nlm.nih.gov/pubmed/1855205 PubMed
MacGregor JI, Jordan VC. Basic guide to the mechanisms of antiestrogen action. Pharmacol Rev. 1998;50: 151–96. Available: http://www.ncbi.nlm.nih.gov/pubmed/9647865 PubMed
Robertson DW, Katzenellenbogen JA, Long DJ, Rorke EA, Katzenellenbogen BS. Tamoxifen antiestrogens. A comparison of the activity, pharmacokinetics, and metabolic activation of the cis and trans isomers of tamoxifen. J Steroid Biochem. 1982;16: 1–13. 10.1016/0022-4731(82)90137-6 PubMed DOI
Katzenellenbogen BS, Norman MJ, Eckert RL, Peltz SW, Mangel WF. Bioactivities, estrogen receptor interactions, and plasminogen activator-inducing activities of tamoxifen and hydroxy-tamoxifen isomers in MCF-7 human breast cancer cells. Cancer Res. 1984;44: 112–119. Available: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=6537799 PubMed
Lim YC, Desta Z, Flockhart DA, Skaar TC. Endoxifen (4-hydroxy-N-desmethyl-tamoxifen) has anti-estrogenic effects in breast cancer cells with potency similar to 4-hydroxy-tamoxifen. Cancer Chemother Pharmacol. 2005;55: 471–478. 10.1007/s00280-004-0926-7 PubMed DOI
Helland T, Gjerde J, Dankel S, Fenne IS, Skartveit L, Drangevåg A, et al. The active tamoxifen metabolite endoxifen (4OHNDtam) strongly down-regulates cytokeratin 6 (CK6) in MCF-7 breast cancer cells. PLoS One. 2015;10: e0122339 10.1371/journal.pone.0122339 PubMed DOI PMC
Johnson MD, Zuo H, Lee KH, Trebley JP, Rae JM, Weatherman R V., et al. Pharmacological characterization of 4-hydroxy-N-desmethyl tamoxifen, a novel active metabolite of tamoxifen. Breast Cancer Res Treat. 2004;85: 151–159. 10.1023/B:BREA.0000025406.31193.e8 PubMed DOI
Dickschen K, Eissing T, Mürdter T, Schwab M, Willmann S, Hempel G. Concomitant use of tamoxifen and endoxifen in postmenopausal early breast cancer: prediction of plasma levels by physiologically-based pharmacokinetic modeling. Springerplus. Springer; 2014;3: 285 10.1186/2193-1801-3-285 PubMed DOI PMC
Hans S, Kaslin J, Freudenreich D, Brand M. Temporally-controlled site-specific recombination in zebrafish. PLoS One. Public Library of Science; 2009;4: e4640 10.1371/journal.pone.0004640 PubMed DOI PMC
Mosimann C, Kaufman CK, Li P, Pugach EK, Tamplin OJ, Zon LI. Ubiquitous transgene expression and Cre-based recombination driven by the ubiquitin promoter in zebrafish. Development. 2011;138: 169–177. 10.1242/dev.059345 PubMed DOI PMC
Hans S, Freudenreich D, Geffarth M, Kaslin J, Machate A, Brand M. Generation of a non-leaky heat shock-inducible Cre line for conditional Cre/lox strategies in zebrafish. Dev Dyn. 2011;240: 108–15. 10.1002/dvdy.22497 PubMed DOI
Felker A, Mosimann C. Contemporary zebrafish transgenesis with Tol2 and application for Cre/lox recombination experiments. Methods Cell Biol. 2016; 10.1016/bs.mcb.2016.01.009 PubMed DOI
Manns JE, Hanks S, Brown JE, Double JA. Methods for liquid chromatographic analysis of tamoxifen, tamoxifen metabolites and their geometric isomers in biological samples. In: Analytical Proceedings. 30(3) [Internet]. 1993 pp. 161–163. Available: http://eurekamag.com/research/032/327/032327157.php
Yu DD, Forman BM. Simple and efficient production of (Z)-4-hydroxytamoxifen, a potent estrogen receptor modulator. J Org Chem. 2003;68: 9489–91. 10.1021/jo035164n PubMed DOI
Robertson DW, Katzenellenbogen JA. Synthesis of the (E) and (Z) isomers of the antiestrogen tamoxifen and its metabolite, hydroxytamoxifen, in tritium-labeled form. J Org Chem. American Chemical Society; 1982;47: 2387–2393. 10.1021/jo00133a030 DOI
Mosimann C, Zon LI. Advanced zebrafish transgenesis with Tol2 and application for Cre/lox recombination experiments. Methods Cell Biol. 2011;104: 173–194. 10.1016/B978-0-12-374814-0.00010-0 PubMed DOI
Lawrence C. Advances in zebrafish husbandry and management. Methods Cell Biol. 2011/09/20 ed. 2011;104: 429–451. doi:B978-0-12-374814-0.00023–9 [pii]10.1016/B978-0-12-374814-0.00023-9 PubMed DOI
Mosimann C, Panáková D, Werdich AA, Musso G, Burger A, Lawson KL, et al. Chamber identity programs drive early functional partitioning of the heart. Nat Commun. Nature Publishing Group; 2015;6 10.1038/ncomms9146 PubMed DOI PMC
Burgess A, Vigneron S, Brioudes E, Labbé J- C, Lorca T, Castro A. Loss of human Greatwall results in G2 arrest and multiple mitotic defects due to deregulation of the cyclin B-Cdc2/PP2A balance. Proc Natl Acad Sci U S A. 2010;107: 12564–9. 10.1073/pnas.0914191107 PubMed DOI PMC
Fauq AH, Maharvi GM, Sinha D. A convenient synthesis of (Z)-4-hydroxy-N-desmethyltamoxifen (endoxifen). Bioorg Med Chem Lett. 2010;20: 3036–8. 10.1016/j.bmcl.2010.03.117 PubMed DOI