Have a personal or library account? Click to login
Effect of selected bisphenol derivatives on nuclear receptor expression in ovarian cell line COV434 Cover

Effect of selected bisphenol derivatives on nuclear receptor expression in ovarian cell line COV434

Open Access
|Nov 2020

References

  1. Alexiadis M, Eriksson N, Jamieson S, Davis M, Drummond AE, Chu S, Clyne CD, Muscat GE, Fuller PJ. Nuclear receptor profiling of ovarian granulosa cell tumors. Horm Cancer 2, 157–169, 2011.10.1007/s12672-011-0069-321761343
  2. Bassett MH, Suzuki T, Sasano H, De Vries CJ, Jimenez PT, Carr BR, Rainey WE. The orphan nuclear receptor NGFIB regulates transcription of 3beta-hydroxysteroid dehydrogenase. Implications for the control of adrenal functional zonation. J Biol Chem 279, 37622–37630, 2004.10.1074/jbc.M40543120015208301
  3. Beard JA, Tenga A, Chen T. The interplay of NR4A receptors and the oncogene-tumor suppressor networks in cancer. Cell Signal 27, 257–266, 2015.10.1016/j.cellsig.2014.11.009427644125446259
  4. Cao Y, Qu X, Ming Z, Yao Y, Zhang Y. The correlation between exposure to BPA and the decrease of the ovarian reserve. Int J Clin Exp Pathol 11, 3375–3382, 2018.
  5. Castellini C, Totaro M, Parisi A, D’Andrea S, Lucente L, Cordeschi G, Francavilla S, Francavilla F, Barbonetti A. Bisphenol A and Male Fertility: Myths and Realities. Front Endocrinol (Lausanne) 11, 353, 2020.10.3389/fendo.2020.00353730433732595601
  6. Castillo Sanchez R, Gomez R, Perez Salazar E. Bisphenol A induces migration through a GPER-, FAK-, Src-, and ERK2-dependent pathway in MDA-MB-231 breast cancer cells. Chem Res Toxicol 29, 285–295, 2016.10.1021/acs.chemrestox.5b0045726914403
  7. Chand AL, Pathirage N, Lazarus K, Chu S, Drummond AE, Fuller PJ, Clyne CD. Liver receptor homologue-1 expression in ovarian epithelial and granulosa cell tumours. Steroids 78, 700–706, 2013.10.1016/j.steroids.2013.03.00123537609
  8. Chen D, Kannan K, Tan H, Zheng Z, Feng YL, Wu Y, Widelka M. Bisphenol analogues other than BPA: environmental occurrence, human exposure, and toxicity-a review. Environ Sci Technol 50, 5438–5453, 2016.10.1021/acs.est.5b0538727143250
  9. Ciucci A, Ferrandina G, Mascilini F, Filippetti F, Scambia G, Zannoni GF, Gallo D. Estrogen receptor β: Potential target for therapy in adult granulosa cell tumors? Gynecol Oncol 150, 158–165, 2018.10.1016/j.ygyno.2018.05.01329786517
  10. Ditsch N, Heublein S, Jeschke U, Sattler C, Kuhn C, Hester A, Czogalla B, Trillsch F, Mahner S, Engel J, Mayr D, Schmoeckel E. Cytoplasmic versus nuclear THR alpha expression determines survival of ovarian cancer patients. J Cancer Res Clin Oncol 146, 1923–1932, 2020.10.1007/s00432-020-03241-7732441532533406
  11. Gerona RR, Pan J, Zota AR, Schwartz JM, Friesen M, Taylor JA, Hunt PA, Woodruff TJ. Direct measurement of Bisphenol A (BPA), BPA glucuronide and BPA sulfate in a diverse and low-income population of pregnant women reveals high exposure, with potential implications for previous exposure estimates: a cross-sectional study. Environ Health 15, 50, 2016.10.1186/s12940-016-0131-2482888827071747
  12. Gorowska-Wojtowicz E, Duliban M, Kudrycka M, Dutka P, Pawlicki P, Milon A, Zarzycka M, Placha W, Kotula-Balak M, Ptak A, Wolski JK, Bilinska B. Leydig cell tumorigenesis - implication of G-protein coupled membrane estrogen receptor, peroxisome proliferator-activated receptor and xenoestrogen exposure. In vivo and in vitro appraisal. Tissue Cell 61, 51–60, 2019.10.1016/j.tice.2019.08.00131759407
  13. Grimaldi M, Boulahtouf A, Toporova L, Balaguer P. Functional profiling of bisphenols for nuclear receptors. Toxicology 420, 39–45, 2019.10.1016/j.tox.2019.04.00330951782
  14. Hui L, Li H, Lu G, Chen Z, Sun W, Shi Y, Fu Z, Huang B, Zhu X, Lu W, Xia D, Wu Y. Low dose of bisphenol A modulates ovarian cancer gene expression profile and promotes epithelial to mesenchymal transition via canonical Wnt pathway. Toxicol Sci 164, 527–538, 2018.10.1093/toxsci/kfy10729718440
  15. Hunakova L, Macejova D, Toporova L, Brtko J. Anticancer effects of tributyltin chloride and triphenyltin chloride in human breast cancer cell lines MCF-7 and MDA-MB-231. Tumour Biol 37, 6701–6708, 2016.10.1007/s13277-015-4524-626662104
  16. Inoue T, Kohro T, Tanaka T, Kanki Y, Li G, Poh HM, Mimura I, Kobayashi M, Taguchi A, Maejima T, Suehiro J, Sugiyama A, Kaneki K, Aruga H, Dong S, Stevens JF, Yamamoto S, Tsutsumi S, Fujita T, Ruan X, Aburatani H, Nangaku M, Ruan Y, Kodama T, Wada Y. Cross-enhancement of ANGPTL4 transcription by HIF1 alpha and PPAR beta/delta is the result of the conformational proximity of two response elements. Genome Biol, 15, R63, 2014.10.1186/gb-2014-15-4-r63405374924721177
  17. Kulus M, Kranc W, Sujka-Kordowska P, Celichowski P, Konwerska A, Jankowski M, Jeseta M, Skowronski MT, Piotrowska-Kempisty H, Bukowska D, Zabel M, Bruska M, Mozdziak P, Kempisty B, Antosik P. Transcriptomic analysis of expression of genes regulating cell cycle progression in porcine ovarian granulosa cells during short-term in vitro primary culture. Histochem Cell Biol 153, 397–412, 2020.10.1007/s00418-020-01860-2729992632157392
  18. Lammel Lindemann JA, Angajala A, Engler DA, Webb P, Ayers SD. Thyroid hormone induction of human cholesterol 7 alpha-hydroxylase (Cyp7a1) in vitro. Mol Cell Endocrinol 388, 32–40, 2014.10.1016/j.mce.2014.02.003418072024582860
  19. Lathi RB, Liebert CA, Brookfield KF, Taylor JA, vom Saal FS, Fujimoto VY, Baker VL. Conjugated bisphenol A in maternal serum in relation to miscarriage risk. Fertil Steril 102, 123–128, 2014.10.1016/j.fertnstert.2014.03.024471126324746738
  20. Lee S, Kim C, Youn H, Choi K. Thyroid hormone disrupting potentials of bisphenol A and its analogues - in vitro comparison study employing rat pituitary (GH3) and thyroid follicular (FRTL-5) cells. Toxicol In Vitro 40, 297–304, 2017.10.1016/j.tiv.2017.02.00428167136
  21. Lefevre L, Authier H, Stein S, Majorel C, Couderc B, Dardenne C, Eddine MA, Meunier E, Bernad J, Valentin A, Pipy B, Schoonjans K, Coste A. LRH-1 mediates anti-inflammatory and antifungal phenotype of IL-13-activated macrophages through the PPARγ ligand synthesis. Nat Commun 6, 6801, 2015.10.1038/ncomms7801441063825873311
  22. Leung DTH, Nguyen T, Oliver EM, Matti J, Alexiadis M, Silke J, Jobling TW, Fuller PJ, Chu S. Combined PPARγ activation and XIAP inhibition as a potential therapeutic strategy for ovarian granulosa cell tumors. Mol Cancer Ther 18, 364–375, 2019.10.1158/1535-7163.MCT-18-007830530769
  23. Liu Y, Deguchi Y, Tian R, Wei D, Wu L, Chen W, Xu W, Xu M, Liu F, Gao S, Jaoude JC, Chrieki SP, Moussalli MJ, Gagea M, Morris J, Broaddus RR, Zuo X, Shureiqi I. Pleiotropic Effects of PPARD Accelerate colorectal tumorigenesis, progression, and invasion. Cancer Res 79, 954–969, 2019.10.1158/0008-5472.CAN-18-1790639766330679176
  24. Livak KJ, Schmittgen TC. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25, 402–408, 2001.10.1006/meth.2001.126211846609
  25. Martin-Martin N, Zabala-Letona A, Fernandez-Ruiz S, Arreal L, Camacho L, Castillo-Martin M, Cortazar AR, Torrano V, Astobiza I, Zuniga-Garcia P, Ugalde-Olano A, Loizaga-Iriarte A, Unda M, Valcarcel-Jimenez L, Arruabarrena-Aristorena A, Piva M, Sanchez-Mosquera P, Aransay AM, Gomez-Munoz A, Barrio R, Sutherland JD, Carracedo A. PPARδ elicits ligand-independent repression of trefoil factor family to limit prostate cancer growth. Cancer Res 78, 399–409, 2018.10.1158/0008-5472.CAN-17-090829187400
  26. Meinsohn MC, Smith OE, Bertolin K, Murphy BD. The orphan nuclear receptors steroidogenic factor-1 and liver receptor homolog-1: structure, regulation, and essential roles in mammalian reproduction. Physiol Rev 99, 1249–1279, 2019.10.1152/physrev.00019.201830810078
  27. Nishizawa H, Morita M, Sugimoto M, Imanishi S, Manabe N. Effects of in utero exposure to bisphenol A on mRNA expression of arylhydrocarbon and retinoid receptors in murine embryos. J Reprod Dev 51, 315–324, 2005.10.1262/jrd.1600815738621
  28. Nomiri S, Hoshyar R, Ambrosino C, Tyler CR, Mansouri B. A minireview of bisphenol A (BPA) effects on cancer-related cellular signaling pathways. Environ Sci Pollut Res Int 26, 8459–8467, 2019.10.1007/s11356-019-04228-930712204
  29. Pei F, Jiang J, Bai S, Cao H, Tian L, Zhao Y, Yang C, Dong H, Ma Y. Chemical-defined and albumin-free generation of human atrial and ventricular myocytes from human pluripotent stem cells. Stem Cell Res 19, 94–103, 2017.10.1016/j.scr.2017.01.00628110125
  30. Peretz J, Vrooman L, Ricke WA, Hunt PA, Ehrlich S, Hauser R, Padmanabhan V, Taylor HS, Swan SH, VandeVoort CA, Flaws JA. Bisphenol a and reproductive health: update of experimental and human evidence, 2007-2013. Environ Health Perspect 122, 775–786, 2014.10.1289/ehp.1307728412303124896072
  31. Renaud L, Huff M, da Silveira WA, Angert M, Haas M, Hardiman G. Genome-wide analysis of low dose bisphenol-A (BPA) exposure in human prostate cells. Curr Genomics 20, 260–274, 2019.10.2174/1389202920666190603123040698395532030086
  32. Rochester J, Bolden A. Bisphenol S and F: A systematic review and comparison of the hormonal activity of bisphenol A substitutes. Environ Health Perspect 123, 643–650, 2015.10.1289/ehp.1408989449227025775505
  33. Safe S, Jin UH, Hedrick E, Reeder A, Lee SO. Minireview: role of orphan nuclear receptors in cancer and potential as drug targets. Mol Endocrinol 28, 157–172, 2014.10.1210/me.2013-1291389663824295738
  34. Sauer SJ, Tarpley M, Shah I, Save AV, Lyerly HK, Patierno SR, Williams KP, Devi GR. Bisphenol A activates EGFR and ERK promoting proliferation, tumor spheroid formation and resistance to EGFR pathway inhibition in estrogen receptor-negative inflammatory breast cancer cells. Carcinogenesis 38, 252–260, 2017.10.1093/carcin/bgx003596374228426875
  35. Scsukova S, Rollerova E, Bujnakova Mlynarcikova A. Impact of endocrine disrupting chemicals on onset and development of female reproductive disorders and hormone-related cancer. Reprod Biol 16, 243–254, 2016.10.1016/j.repbio.2016.09.00127692877
  36. Shah K, Faridi J. Estrogen, tamoxifen, and Akt modulate expression of putative housekeeping genes in breast cancer cells. J Steroid Biochem Mol Biol 125, 219–225, 2011.10.1016/j.jsbmb.2011.03.00521420492
  37. Sharma S, Ahmad S, Khan MF, Parvez S, Raisuddin S. In silico molecular interaction of bisphenol analogues with human nuclear receptors reveals their stronger affinity vs. classical bisphenol A. Toxicol Mech Methods 28, 660–669, 2018.10.1080/15376516.2018.149166329925285
  38. Toporova L, Balaguer P. Nuclear receptors are the major targets of endocrine disrupting chemicals. Mol Cell Endocrinol 502, 110665, 2020.10.1016/j.mce.2019.11066531760044
  39. Vissenberg R, Manders VD, Mastenbroek S, Fliers E, Afink GB, Ris-Stalpers C, Goddijn M, Bisschop PH. Patho-physiological aspects of thyroid hormone disorders/thyroid peroxidase autoantibodies and reproduction. Hum Reprod Update 21, 378–387, 2015.10.1093/humupd/dmv00425634660
  40. Wu F, Zhao J, Zhang E, Wu Q, Wu X, Zhang D, Liu Y, Wang R, Li W. Bisphenol A affects ovarian development in adolescent mice caused by genes expression change. Gene 740, 144535, 2020.10.1016/j.gene.2020.14453532156529
  41. Wu S, Zhang D, Zhang ZP, Soprano DR, Soprano KJ. Critical role of both retinoid nuclear receptors and retinoid-X-receptors in mediating growth inhibition of ovarian cancer cells by all-trans retinoic acid. Oncogene 17, 2839–2849, 1998.10.1038/sj.onc.12022089879990
  42. Wu S, Sun H, Zhang Q, Jiang Y, Fang T, Cui I, Yan G, Hu Y. MicroRNA-132 promotes estradiol synthesis in ovarian granulosa cells via translational repression of Nurr1. Reprod Biol Endocrinol 13, 94, 2015.10.1186/s12958-015-0095-z
  43. Wu Y, Ghosh S, Nishi Y, Yanase T, Nawata H, Hu T. The orphan nuclear receptors NURR1 and NGFI-B modulate aromatase gene expression in ovarian granulosa cells: a possible mechanism for repression of aromatase expression upon luteinizing hormone surge. Endocrinology 146, 237–246, 2005.10.1210/en.2004-0889
  44. Yanase T, Mu YM, Nishi Y, Goto K, Nomura M, Okabe T, Takayanagi R, Nawata H. Regulation of aromatase by nuclear receptors. J Steroid Biochem Mol Biol 79, 187–192, 2001.10.1016/S0960-0760(01)00161-3
  45. Yoo SW, Savchev S, Sergott L, Rezai T, Lopez MF, Von Wald T, Eaton JL, Reindollar R, Usheva A. A large network of interconnected signaling pathways in human ovarian follicles is supported by the gene expression activity of the granulosa cells. Reprod Sci 18, 476–484, 2011.10.1177/193371911038884821558463
  46. Ziv-Gal A, Flaws JA. Evidence for bisphenol A-induced female infertility: a review (2007-2016). Fertil Steril 106, 827–856, 2016.10.1016/j.fertnstert.2016.06.027502690827417731
DOI: https://doi.org/10.2478/enr-2020-0031 | Journal eISSN: 1336-0329 | Journal ISSN: 1210-0668
Language: English
Page range: 275 - 283
Published on: Nov 24, 2020
Published by: Slovak Academy of Sciences, Institute of Experimental Endocrinology
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2020 Alzbeta Bujnakova Mlynarcikova, Sona Scsukova, published by Slovak Academy of Sciences, Institute of Experimental Endocrinology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.