참고문헌
- Anstead GM, Carlson KE, Katzenellenbogen JA (1997). The estradiol pharmacophore: ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site. Steroids, 62, 268-303. https://doi.org/10.1016/S0039-128X(96)00242-5
- Arnal JF, Valera MC, Payrastre B, et al (2012). Structure-function relationship of estrogen receptors in cardiovascular pathophysiological models. Thromb Res, 130, 7-11. https://doi.org/10.1016/j.thromres.2011.09.022
- Ascenzi P, Bocedi A, Marino M (2006). Structure-function relationship of estrogen receptor alpha and beta: impact on human health. Mol Aspects Med, 27, 299-402. https://doi.org/10.1016/j.mam.2006.07.001
- Barkhem T, Carlsson B, Nilsson Y, et al (1998). Differential response of estrogen receptor alpha and estrogen receptor beta to partial estrogen agonists/antagonists. Mol Pharmacol, 54, 105-12.
- Berman HM, Westbrook J, Feng Z, et al (2000). The Protein Data Bank. Nucleic Acids Res, 28, 235-42. https://doi.org/10.1093/nar/28.1.235
- Bollig-Fischer A, Thakur A, Sun Y, et al (2012). The Predominant Proteins that React to the MC-20 Estrogen Receptor Alpha Antibody Differ in Molecular Weight between the Mammary Gland and Uterus in the Mouse and Rat. Int J Biomed Sci, 8, 51-63.
- Brzozowski AM, Pike AC, Dauter Z, et al (1997). Molecular basis of agonism and antagonism in the oestrogen receptor. Nature, 389, 753-8. https://doi.org/10.1038/39645
- Cao X, Jiang J, Zhang S, et al (2013). Discovery of natural estrogen receptor modulators with structure-based virtual screening. Bioorg Med Chem Lett, 23, 3329-33. https://doi.org/10.1016/j.bmcl.2013.03.105
- Chakraborty S, Cole S, Rader N, et al (2012). In silico design of peptidic inhibitors targeting estrogen receptor alpha dimer interface. Mol Divers, 16, 441-51. https://doi.org/10.1007/s11030-012-9378-x
- Chitrala KN, Yeguvapalli S (2013). Prediction and analysis of ligands against estrogen related receptor alpha. Asian Pac J Cancer Prev, 14, 2371-5. https://doi.org/10.7314/APJCP.2013.14.4.2371
- Czeczuga-Semeniuk E, Jarzabek K, Lemancewicz D, et al (2009). The vitamin A family can significantly decrease the expression of ERbeta of ERs positive breast cancer cells in the presence or absence of ER ligands and paclitaxel. Gynecol Endocrinol, 25, 287-93. https://doi.org/10.1080/09513590802530924
- D'Amelio P, Isaia GC (2013). The use of raloxifene in osteoporosis treatment. Expert Opin Pharmacother, 14, 949-56. https://doi.org/10.1517/14656566.2013.782002
- de Villiers TJ, Gass ML, Haines CJ, et al (2013). Global Consensus Statement on menopausal hormone therapy. Maturitas, 74, 391-2. https://doi.org/10.1016/j.maturitas.2013.02.001
- Eliassen AH, Hendrickson SJ, Brinton LA, et al (2012). Circulating carotenoids and risk of breast cancer: pooled analysis of eight prospective studies. J Natl Cancer Inst, 104, 1905-16. https://doi.org/10.1093/jnci/djs461
- Frasor J, Barnett DH, Danes JM, et al (2003). Response-specific and ligand dose-dependent modulation of estrogen receptor (ER) alpha activity by ERbeta in the uterus. Endocrinol, 144, 3159-66. https://doi.org/10.1210/en.2002-0143
- Gangloff M, Ruff M, Eiler S, et al (2001). Crystal structure of a mutant hERalpha ligand-binding domain reveals key structural features for the mechanism of partial agonism. J Biol Chem, 276, 15059-65. https://doi.org/10.1074/jbc.M009870200
- Gaudet P, Lane L, Fey P, et al (2009). Collaborative annotation of genes and proteins between UniProtKB/Swiss-Prot and dictyBase. Database (Oxford), 2009, 16.
- Hendrickson SJ, Hazra A, Chen C, et al (2012). beta-Carotene 15,15'-monooxygenase 1 single nucleotide polymorphisms in relation to plasma carotenoid and retinol concentrations in women of European descent. Am J Clin Nutr, 96, 1379-89. https://doi.org/10.3945/ajcn.112.034934
- Illera JC, Perez-Alenza MD, Nieto A, et al (2006). Steroids and receptors in canine mammary cancer. Steroids, 71, 541-8. https://doi.org/10.1016/j.steroids.2005.11.007
- Kuiper G, Carlsson B, Grandien K, et al (1997). Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta. Endocrinol, 138, 863-70.
- Kumar R, Thompson EB (1999). The structure of the nuclear hormone receptors. Steroids, 64, 310-9. https://doi.org/10.1016/S0039-128X(99)00014-8
- Kumar R, Zakharov MN, Khan SH, et al (2011). The dynamic structure of the estrogen receptor. J Amino Acids, 2011, 812540.
- LaFrate AL, Carlson KE, Katzenellenbogen JA (2009). Steroidal bivalent ligands for the estrogen receptor: design, synthesis, characterization and binding affinities. Bioorg Med Chem, 17, 3528-35. https://doi.org/10.1016/j.bmc.2009.04.016
- Leinonen R, Nardone F, Zhu W, et al (2006). UniSave: the UniProtKB sequence/annotation version database. Bioinformatics, 22, 1284-5. https://doi.org/10.1093/bioinformatics/btl105
- Lewis DF, Ogg MS, Goldfarb PS, et al (2002). Molecular modelling of the human glucocorticoid receptor (hGR) ligand-binding domain (LBD) by homology with the human estrogen receptor alpha (hERalpha) LBD: quantitative structure-activity relationships within a series of CYP3A4 inducers where induction is mediated via hGR involvement. J Steroid Biochem Mol Biol, 82, 195-9. https://doi.org/10.1016/S0960-0760(02)00158-9
- Li X, Huang J, Yi P, et al (2004). Single-chain estrogen receptors (ERs) reveal that the ERalpha/beta heterodimer emulates functions of the ERalpha dimer in genomic estrogen signaling pathways. Mol Cell Biol, 24, 7681-94. https://doi.org/10.1128/MCB.24.17.7681-7694.2004
- Madeira KP, Daltoe RD, Sirtoli GM, et al (2012). Comparison of immunohistochemical analysis with estrogen receptor SP1 and 1D5 monoclonal antibodies in breast cancer. Pathol Res Pract, 208, 657-61. https://doi.org/10.1016/j.prp.2012.07.010
- Maggiolini M, Bonofiglio D, Marsico S, et al (2001). Estrogen receptor alpha mediates the proliferative but not the cytotoxic dose-dependent effects of two major phytoestrogens on human breast cancer cells. Mol Pharmacol, 60, 595-602.
- Meshram RJ, Bhiogade NH, Gacche RN, et al (2012). Virtual screening and docking exploration on estrogen receptor: An in silico approach to decipher novel anticancer agents. Indian J Biotechnol, 11, 389-95.
- Millanta F, Calandrella M, Bari G, et al (2005). Comparison of steroid receptor expression in normal, dysplastic, and neoplastic canine and feline mammary tissues. Res Vet Sci, 79, 225-32. https://doi.org/10.1016/j.rvsc.2005.02.002
- Nam K, Marshall P, Wolf RM, et al (2003). Simulation of the different biological activities of diethylstilbestrol (DES) on estrogen receptor alpha and estrogen-related receptor gamma. Biopolymers, 68, 130-8. https://doi.org/10.1002/bip.10307
- Nam KH, Huang Q, Ke A (2012). Nucleic acid binding surface and dimer interface revealed by CRISPR-associated CasB protein structures. FEBS Lett, 586, 3956-61. https://doi.org/10.1016/j.febslet.2012.09.041
- Nose T, Tokunaga T, Shimohigashi Y (2009). Exploration of endocrine-disrupting chemicals on estrogen receptor alpha by the agonist/antagonist differential-docking screening (AADS) method: 4-(1-adamantyl)phenol as a potent endocrine disruptor candidate. Toxicol Lett, 191, 33-9. https://doi.org/10.1016/j.toxlet.2009.08.001
- Osborne CK, Zhao H, Fuqua SA (2000). Selective estrogen receptor modulators: structure, function, and clinical use. J Clin Oncol, 18, 3172-86.
- Pieper U, Eswar N, Braberg H, et al (2004). MODBASE, a database of annotated comparative protein structure models, and associated resources. Nucleic Acids Res, 32, 217-22.
- Pike AC, Brzozowski AM, Hubbard RE, et al (1999). Structure of the ligand-binding domain of oestrogen receptor beta in the presence of a partial agonist and a full antagonist. EMBO J, 18, 4608-18. https://doi.org/10.1093/emboj/18.17.4608
- Rehm S, Solleveld HA, Portelli ST, et al (2007). Histologic changes in ovary, uterus, vagina, and mammary gland of mature beagle dogs treated with the SERM idoxifene. Birth Defects Res B Dev Reprod Toxicol, 80, 225-32. https://doi.org/10.1002/bdrb.20119
- Rustici G, Kolesnikov N, Brandizi M, et al (2013). ArrayExpress update--trends in database growth and links to data analysis tools. Nucleic Acids Res, 41, 987-90. https://doi.org/10.1093/nar/gks1174
- Rybalchenko V, Grillo MA, Gastinger MJ, et al (2009). The unliganded long isoform of estrogen receptor beta stimulates brain ryanodine receptor single channel activity alongside with cytosolic Ca2+. J Recept Signal Transduct Res, 29, 326-41. https://doi.org/10.3109/10799890903295168
- Schnell S, Mendoza C (2001). A fast method to estimate kinetic constants for enzyme inhibitors. Acta Biotheor, 49, 109-13. https://doi.org/10.1023/A:1010219527831
- Shiau AK, Barstad D, Loria PM, et al (1998). The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen. Cell, 95, 927-37. https://doi.org/10.1016/S0092-8674(00)81717-1
- Sievers F, Wilm A, Dineen D, et al (2011). Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega. Mol Syst Biol, 7, 539.
- Stump AL, Kelley KW, Wensel TM (2007). Bazedoxifene: a third-generation selective estrogen receptor modulator for treatment of postmenopausal osteoporosis. Ann Pharmacother, 41, 833-9. https://doi.org/10.1345/aph.1H428
- Suganya J, Radha M, Naorem DL, et al (2014). In Silico docking studies of selected flavonoids-- natural healing agents against breast cancer. Asian Pac J Cancer Prev, 15, 8155-9. https://doi.org/10.7314/APJCP.2014.15.19.8155
- Thompson JD, Higgins DG, Gibson TJ (1994). CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res, 22, 4673-80. https://doi.org/10.1093/nar/22.22.4673
- Toniti W, Suthiyotha N, Puchadapirom P, et al (2011). Binding capacity of ER-alpha ligands and SERMs: comparison of the human, dog and cat. Asian Pac J Cancer Prev, 12, 2875-9.
- Touraine P (2003). [SERMs and uterus]. Ann Med Interne (Paris), 154, 103-8.
- Tremollieres F, Lopes P (2002). [Specific estrogen receptor modulators (SERMs)]. Presse Med, 31, 1323-8.
- UniProt C (2014). Activities at the Universal Protein Resource (UniProt). Nucleic Acids Res, 42, 191-8. https://doi.org/10.1093/nar/gkt1140
- Xu CY, Jiang ZN, Zhou Y, et al (2013). Estrogen receptor alpha roles in breast cancer chemoresistance. Asian Pac J Cancer Prev, 14, 4049-52. https://doi.org/10.7314/APJCP.2013.14.7.4049
- Zhang X, Spiegelman D, Baglietto L, et al (2012). Carotenoid intakes and risk of breast cancer defined by estrogen receptor and progesterone receptor status: a pooled analysis of 18 prospective cohort studies. Am J Clin Nutr, 95, 713-25. https://doi.org/10.3945/ajcn.111.014415
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