The DOI matches its Crossref record.
Fast and easy in vitro screening assay for cholesterol biosynthesis inhibitors in the post-squalene pathway
Abstract
A whole-cell assay for screening cholesterol biosynthesis inhibitors in the post-squalene pathway has been developed. HL 60 cells were incubated for 24h with test substances. The nonsaponifiable lipids were extracted by means of liquid-liquid extraction using tert-butylmethylether. The raw extracts were purified by dispersive solid phase extraction using a primary-secondary amine material (PSA) and dried using sodium sulphate. The sterols were derivatized using N-trimethylsilylimidazole. GLC/MS analysis was carried out in less than 12.5 min using fast GLC mode. The obtained sterol patterns indicated which enzyme had been inhibited. Specific sterol patterns which reflect the different enzyme inhibitions were obtained using established inhibitors of cholesterol biosynthesis like AY 9944, NB 598, clotrimazole, aminotriazole and DR 258, a Delta24-reductase inhibitor prepared in our working group. For characterizing IC(50) values we used sodium 2-(13)C-acetate and quantified the incorporation of it into cholesterol relative to control levels after the samples had been normalized to their protein content.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Sterols were identified based on their relative retention time and comparison of electron ionization mass spectra (Giera et al., 2007, Müller et al., 2017).”
From Cholesterol Metabolism Is a Druggable Axis that Independently Regulates Tau and Amyloid-β in iPSC-Derived Alzheimer’s Disease Neurons (2019) · cites this paper as Giera et al., 2007
Citations
Cites
No references could be resolved yet.
Research works printed but not linked: 40
- Grundy, 2004, Implications of recent clinical trials fort the national cholesterol education program adult treatment panel III guidelines, J Am Coll Cardiol, 44, 720, 10.1016/j.jacc.2004.07.001 · DOI · Paper page
- Bellosta, 2004, Safety of statins focus on clinical pharmacokinetics and drug interactions, Circulation, 109, III-50, 10.1161/01.CIR.0000131519.15067.1f · DOI · Paper page
- Huff, 2005, Lord of the rings—the mechanisms for oxidosqualene:lanosterol cyclase becomes crystal clear, Trends Phamacol Sci, 26, 335, 10.1016/j.tips.2005.05.004 · DOI
- Wolf, 1999, The function of cholesterol in embryogenesis, J Nutr Biochem, 10, 188, 10.1016/S0955-2863(98)00102-8 · DOI
- Waterham, 2000, Biochemical and genetic aspects of 7-dehydrocholesterol reductase and Smith–Lemli–Opitz syndrome, Biochim Biophys Acta, 1529, 340, 10.1016/S1388-1981(00)00159-1 · DOI
- Herman, 2003, Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes, Hum Mol Gen, 12, R75, 10.1093/hmg/ddg072 · DOI
- Aufenanger, 1986, The effects of BM 15.766 an inhibitor of 7-dehydrocholesterol Δ7-reductase, on cholesterol biosynthesis in primary rat hepatocytes, Biochem Pharmacol, 35, 911, 10.1016/0006-2952(86)90076-6 · DOI
- Pill, 1987, Thin-layer chromatography of radioactively labelled cholesterol and precursors from biological material, Fresenius Z Anal Chem, 327, 558, 10.1007/BF00487248 · DOI
- Eisele, 1997, Effects of a novel 2,3-oxidosqualene cyclase inhibitor on cholesterol biosynthesis and lipid metabolism in vivo, J Lipid Res, 38, 564, 10.1016/S0022-2275(20)37264-3 · DOI
- Fernández, 2002, Inhibition of cholesterol biosynthesis by Δ22-unsaturated phytosterols via competitive inhibition of sterol Δ24-reductase in mammalian cells, Biochem J, 366, 109, 10.1042/bj20011777 · DOI
- Lewis, 1995, Enzyme inhibition during the conversion of squalene to cholesterol, Steroids, 60, 475, 10.1016/0039-128X(95)00054-T · DOI
- Harwood, 2005, Dual-action hypoglycemic and hypocholesterolemic agents that inhibit glycogen phosphorylase and lanosterol demethylase, J Lipid Res, 46, 547, 10.1194/jlr.M400436-JLR200 · DOI
- Wolff Briche, 2002, Comparison of gas chromatography and liquid chromatography mass spectrometric measurements for high accuracy analysis of cholesterol in human serum by isotope dilution mass spectrometry, Rapid Commun Mass Spectrom, 16, 848, 10.1002/rcm.646 · DOI
- De Zeeuw, 2006, Fast, practical GC and GC–MS, Am Lab, 38, 26
- Plössl, 2006, Multiresidue analytical method using dispersive solid-phase extraction and gas chromatography/ion trap mass spectrometry to determine pharmaceuticals in whole blood, J Chromatogr A, 1135, 19, 10.1016/j.chroma.2006.09.033 · DOI
- Lee, 1996, Stable isotopes and mass isotopomer study of fatty acid and cholesterol synthesis. A review of the MIDA Approach, Adv Exp Med Biol, 399, 95, 10.1007/978-1-4613-1151-5_8 · DOI
- Kelleher, 1994, Isotopomer spectral analysis of cholesterol synthesis: applications in human hepatoma cells, Am J Physiol Endocrinol Metab, 266, E384, 10.1152/ajpendo.1994.266.3.E384 · DOI
- Holleran, 1998, Effect of tamoxifen on cholesterol synthesis in HepG2 cells and cultured rat hepatocytes, Metabolism, 47, 1504, 10.1016/S0026-0495(98)90078-6 · DOI
- Di Buono, 2000, Comparison of deuterium incorporation and mass isotopomer distribution analysis for measurement of human cholesterol biosynthesis, J Lipid Res, 41, 1516, 10.1016/S0022-2275(20)33464-7 · DOI
- Lindenthal, 2002, Isotopomer spectral analysis of intermediates of cholesterol synthesis in human subjects and hepatic cells, Am J Physiol Endocrinol Metab, 282, 1222, 10.1152/ajpendo.00324.2001 · DOI
- Mark, 1996, Effects of a novel 2,3-oxidosqualene cyclase inhibitor on the regulation of cholesterol biosynthesis in HepG2 cells, J Lipid Res, 37, 148, 10.1016/S0022-2275(20)37643-4 · DOI
- Fernández, 2005, Effects of distal cholesterol biosynthesis inhibitors on cell proliferation and cell cycle progression, J Lipid Res, 46, 920, 10.1194/jlr.M400407-JLR200 · DOI
- Bae, 1999, Cholesterol biosynthesis from lanosterol. Molecular cloning, tissue distribution, expression, chromosomal localization, and regulation of rat 7-dehydrocholesterol reductase, a Smith–Lemli–Opitz syndrome related protein, J Biol Chem, 274, 14624, 10.1074/jbc.274.21.14624 · DOI
- Sawada, 2004, biological activity of a novel squalene epoxidase inhibitor, FR194738, Bioorg Med Chem Lett, 14, 633, 10.1016/j.bmcl.2003.11.072 · DOI
- Horie, 1990, NB-598: a potent competitive inhibitor of squalene epoxidase, J Biol Chem, 265, 18075, 10.1016/S0021-9258(17)44716-8 · DOI
- Kraemer, 1986, Effects of ketoconazole on cholesterol synthesis, J Pharmacol Exp Ther, 238, 905
- Beynen, 1981, Inhibition of lipogenesis in isolated hepatocytes by 3-amino-1,2,4-triazole, Toxicology, 22, 171, 10.1016/0300-483X(81)90116-5 · DOI
- Hashimoto, 1991, Identification of intermediates after inhibition of cholesterol synthesis by aminotriazole treatment in vivo, Biochim Biophys Acta, 1086, 115, 10.1016/0005-2760(91)90162-B · DOI
- Ogihara, 1988, Facile synthesis of zymosterol and related compounds, Chem Pharm Bull, 36, 2724, 10.1248/cpb.36.2724 · DOI
- Gerst, 1997, An updated look at the analysis of unsaturated C27 sterols by gas chromatography and mass spectrometry, J Lipid Res, 38, 1685, 10.1016/S0022-2275(20)37187-X · DOI
- Bradford, 1976, A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein–dye binding, Anal Biochem, 72, 248, 10.1016/0003-2697(76)90527-3 · DOI · Paper page
- Ceruti, 1988, Stereospecific synthesis of squalenoid epoxide vinyl ethers as inhibitors of 2,3-oxidosqualene cyclase, J Chem Soc, Perkin Trans, 1, 461, 10.1039/P19880000461 · DOI
- Boer, 2000, Calculated heats of formation of sterol diene isomers compared with synthetic yields of isomerisation reactions of Δ5,7 sterols, J Chem Soc, Perkin Trans, 2, 1701, 10.1039/b002212h · DOI
- Seto, 2000, Stereo and chemical course of acid-catalyzed double bond migration of cholesta-5,7-dien-3β-ol to 5α-cholesta-8,14-dien-3β-ol, J Chem Soc, Perkin Trans, 1, 1679
- Watkinson, 1971, The formation and reduction of the 14,15-double bond in cholesterol biosynthesis, Biochem J, 121, 131, 10.1042/bj1210131 · DOI
- Tsuda, 1979, Carbon-13 nuclear magnetic resonance studies of C27 sterol precursors of cholesterol, J Org Chem, 44, 1290, 10.1021/jo01322a022 · DOI
- Wilson, 1996, Analysis of unsaturated C27 sterols by nuclear magnetic resonance spectroscopy, J Lipid Res, 37, 1529, 10.1016/S0022-2275(20)39137-9 · DOI
- Dolle, 1991, Synthesis of a tritiated 3-dehydroecdysteroid putative precursor of ecdysteroid biosynthesis in locusta migratoria, Tetrahedron, 47, 7067, 10.1016/S0040-4020(01)96161-7 · DOI
- Emmons, 1989, 1H and 13C NMR assignments for lanostan-3β-ol derivatives: revised assignments for lanosterol, Magn Reson Chem, 27, 1012, 10.1002/mrc.1260271103 · DOI
- Mitropoulos, 1976, Effect of triarimol on cholesterol biosynthesis in rat-liver subcellular fractions, Biochem Biophys Res Commun, 71, 892, 10.1016/0006-291X(76)90915-3 · DOI
Cited by
Sorted by citations
van der Kant, R., Langness, V. F., Herrera, C. M., Williams, D. A., Fong, L. K., Leestemaker, Y., Steenvoorden, E., Rynearson, K. D., Brouwers, J. F., Helms, J. B., et al. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2018.12.013 · Cited by 350
Self-citationAccumulation of 8,9-unsaturated sterols drives oligodendrocyte formation and remyelination
Hubler, Z., Allimuthu, D., Bederman, I., Elitt, M. S., Madhavan, M., Allan, K. C., Shick, H. E., Garrison, E., T. Karl, M., Factor, D. C., et al. (2018) · Nature · doi:10.1038/s41586-018-0360-3 · Cited by 226
Self-citationAtypical Antipsychotics Alter Cholesterol and Fatty Acid Metabolism in Vitro
Canfrán-Duque, A., Casado, M. E., Pastor, Ó., Sánchez-Wandelmer, J., de la Peña, G., Lerma, M., Mariscal, P., Bracher, F., Lasunción, M. A., & Busto, R. (2013) · Journal of Lipid Research · doi:10.1194/jlr.m026948 · Cited by 105
Self-citationHaloperidol Disrupts Lipid Rafts and Impairs Insulin Signaling in SH-SY5Y Cells
Sánchez-Wandelmer, J., Dávalos, A., de la Peña, G., Cano, S., Giera, M., Canfrán-Duque, A., Bracher, F., Martín-Hidalgo, A., Fernández-Hernando, C., Lasunción, M. A., et al. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.01.051 · Cited by 49
An Antifungal Benzimidazole Derivative Inhibits Ergosterol Biosynthesis and Reveals Novel Sterols
Keller, P., Müller, C., Engelhardt, I., Hiller, E., Lemuth, K., Eickhoff, H., Wiesmüller, K.-H., Burger-Kentischer, A., Bracher, F., & Rupp, S. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00640-15 · Cited by 50
Self-citation
Metadata
- Authors
- Giera, M., Plössl, F., & Bracher, F.
- Venue
- Steroids
- Publisher
- Elsevier BV
- Published
- 2007-07
- Volume
- 72
- Issue
- 8
- Pages
- 633-642
- ISSN
- 0039-128X
- Cited by
- 44
- References
- 0
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review