Medikamentozno zdravljenje endometrioze: pregled stanja in nove možnosti zdravljenja

In: Slovenian Medical Journal · 2016 · vol. 85(7-8) · doi:10.6016/zdravvestn.1416 · W2769469379
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This review examines current pharmacological treatments for endometriosis, including NSAIDs, oral contraceptives, and progestins, and discusses novel agents targeting inflammation, hormonal systems, and other pathophysiological processes.

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This paper is a review of current and emerging pharmacological treatments for endometriosis, outlining when medication is used (e.g., empirical treatment for pelvic pain with normal gynecologic examination, recurrence after surgery, or as an adjunct to surgical care) and comparing first- and second-line approaches. It reports that in routine practice non-steroidal anti-inflammatory drugs, oral contraceptives, and progestins are commonly used first-line, while gonadoliberin (GnRH) agonists are described as second-line but discouraged. Beyond standard hormone and anti-inflammatory strategies, the review groups newer candidate therapies by targeted pathways including immune dysregulation, reduced apoptosis, increased angiogenesis, extracellular matrix degradation, oxidative stress, and epigenetic changes, while emphasizing that implementation into routine use requires more convincing clinical studies. This paper is centrally about endometriosis — a state-of-the-art review of pharmacological treatment options and emerging therapeutic targets.

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Abstract

Endometriosis is a gynecological disease that is defined as the presence of endometrium-like tissue outside the uterine cavity, and it is one of the main causes of female infertility. Although there is unfortunately no known ‘optimal’ treatment for endometriosis, there are three treatment options: medication, surgical treatment, and a combination of both. The gold standard for diagnosis of endometriosis is a diagnostic laparoscopy, which is also therapeutic. Indications for pharmacological treatment of endometriosis include empirical treatment for patients with pelvic pain who are normal on gynecological examination, or who have recurrent disease after surgical treatment or in combination with surgical treatment. In everyday practice, non-steroid anti-inflammatory drugs, oral contraceptives, and progestins per os are used as first-line pharmacological treatments of endometriosis. Gonadoliberin agonists can be used as second-line treatment, although their use is discouraged. These medications can be used alone or in combination. Studies over the last 10 years have shown that many other agents have potential for treatment of endometriosis. These can be broadly classified into several groups: anti-inflammatory agents, and agents that interfere with the hormonal system, or with other pathophysiological processes, such as a disturbed immune system, reduced apoptosis, enhanced angiogenesis, degradation of the extracellular matrix, increased oxidative stress, and epigenetic changes. However, their introduction into routine use requires more convincing clinical studies to confirm their effectiveness.
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Pharmacological treatment of endometriosis: review of current and new options for treatment DOI: https://doi.org/10.6016/ZdravVestn.1416Keywords: pharmacological treatment, anti-inflammatory agents, hormone therapy, anti-angiogenic agents, antioxidants, histone deacetylase inhibitors.Abstract Endometriosis is a gynecological disease that is defined as the presence of endometrium-like tissue outside the uterine cavity, and it is one of the main causes of female infertility. Although there is unfortunately no known ‘optimal’ treatment for endometriosis, there are three treatment options: medication, surgical treatment, and a combination of both. The gold standard for diagnosis of endometriosis is a diagnostic laparoscopy, which is also therapeutic. Indications for pharmacological treatment of endometriosis include empirical treatment for patients with pelvic pain who are normal on gynecological examination, or who have recurrent disease after surgical treatment or in combination with surgical treatment. In everyday practice, non-steroid anti-inflammatory drugs, oral contraceptives, and progestins per os are used as first-line pharmacological treatments of endometriosis. Gonadoliberin agonists can be used as second-line treatment, although their use is discouraged. These medications can be used alone or in combination. Studies over the last 10 years have shown that many other agents have potential for treatment of endometriosis. These can be broadly classified into several groups: anti-inflammatory agents, and agents that interfere with the hormonal system, or with other pathophysiological processes, such as a disturbed immune system, reduced apoptosis, enhanced angiogenesis, degradation of the extracellular matrix, increased oxidative stress, and epigenetic changes. However, their introduction into routine use requires more convincing clinical studies to confirm their effectiveness. Downloads References Vercellini P, Viganò P, Somigliana E, Fedele L. Endometriosis: pathogenesis and treatment. Nat Rev Endocrinol. 2014; 10 (5): 261–75. Kvaskoff M, Mu F, Terry KL, Harris HR, Poole EM, Farland L, et al. Endometriosis: a high-risk population for major chronic diseases? Hum Reprod Update. 2015; 21 (4): 500–16. Hjordt Hansen MV, Dalsgaard T, Hartwell D, Skovlund CW, Lidegaard O. Reproductive prognosis in endometriosis. A national cohort study. Acta Obstet Gynecol Scand. 2014; 93 (5): 483–9. Signorile PG, Baldi A. New evidence in endometriosis. Int J Biochem Cell Biol. 2015; 60: 19–22. Mohar J, Mojca Böhm M, Vogler A. Pogostnost endometrioze pri zdravih in neplodnih ženskah. Med Razgl. 2004; 43: 193–201. Djokovic D, Calhaz-Jorge C. Somatic stem cells and their dysfunction in endometriosis. Front Surg. 2015; 1: 51. Jerman LF, Hey-Cunningham AJ. Te role of the lymphatic system in endometriosis: a comprehensive review of the literature. Biol Reprod. 2015; 92 (3): 64. Lanišnik Rižner T, Ribič–Pucelj M. Estrogeni in endometrioza. Med Razgl. 2010; 49 (3): 263–74. Viganò P, Parazzini F, Somigliana E, Vercellini P. Endometriosis: epidemiology and aetiological factors. Best Pract Res Clin Obstet Gynaecol. 2004; 18 (2): 177–200. D’Hooghe TM, Debrock S. Endometriosis, retrograde menstruation and peritoneal inflammation in women and in baboons. Hum Reprod Update. 2002; 8 (1): 84–8. Gargett CE, Schwab KE, Brosens JJ, Puttemans P, Benagiano G, Brosens I. Potential role of endometrial stem/progenitor cells in the pathogenesis of early-onset endometriosis. Mol Hum Reprod. 2014; 20 (7): 591–8. Slabe N, Košir R, Meden-Vrtovec H. Sodobni pogled na etiopatogenezo endometrioze. Zdrav Vestn. 2009; 78 (6/7): 315–9. Montgomery GW, Nyholt DR, Zhao ZZ, Treloar SA, Painter JN, Missmer SA, et al. Te search for genes contributing to endometriosis risk. Hum Reprod Update. 2008; 14 (5): 447–457. Porpora MG, Resta S, Fuggetta E, Storelli P, Megiorni F, Manganaro L, et al. Role of environmental organochlorinated pollutants in the development of endometriosis. Clin Exp Obstet Gynecol. 2013; 40 (4): 565–567. Uzunçakmak C, Güldaş A, Ozçam H, Dinç K. Scar endometriosis: a case report of this uncommon entity and review of the literature. Case Rep Obstet Gynecol. 2013; 2013: 386783. Anderson TL, Aguirre F, Ayuso A. Diaphragmatic endometriosis in a patient with cyclic shoulder pain. J Minim Invasive Gynecol. 2014; 21 (1): 23–4. Azizad-Pinto P, Clarke D. Toracic endometriosis syndrome: case report and review of the literature. Perm J. 2014; 18 (3): 61–5. Haas D, Shebl O, Shamiyeh A, Oppelt P. Te rASRM score and the Enzian classifcation for endometriosis: their strengths and weaknesses. Acta Obstet Gynecol Scand. 2013; 92 (1): 3–7. Hsiao KY, Lin SC, Wu MH, Tsai SJ. Pathological functions of hypoxia in endometriosis. Front Biosci (Elite Ed). 2015; 7: 309–21. Jarząbek-Bielecka G, Radomski D, Pawlaczyk M, Friebe Z, Biedermann K. Dyspareunia as a sexual problem in women with endometriosis. Archives of Perinatal Medicine. 2010; 16 (1): 51–3. Vogler A, Ribič-Pucelj M, Tomaževič T. Kirurško zdravljenje endometrioze pri neplodnih bolnicah. Zdrav Vestn. 2003; 72: II-117–20. Kodaman PH. Current strategies for endometriosis management. Obstet Gynecol Clin North Am. 2015; 42 (1): 87–101. Mettler L, Ruprai R, Alkatout I. Impact of medical and surgical treatment of endometriosis on the cure of endometriosis and pain. Biomed Res Int. 2014; 2014: 264653. Hamdan M, Omar SZ, Dunselman G, Cheong Y. Influence of endometriosis on assisted reproductive technology outcomes: a systematic review and meta-analysis. Obstet Gynecol. 2015; 125 (1): 79–88. Herzog M, Pavšlar K, Vogler A. Vpliv endometrioze na uspešnost zunajtelesne oploditve. Zdrav Vestn. 2012; 81 (6): 453–60. Chiang HJ, Lin PY, Huang FJ, Kung FT, Lin YL, Sung PH, et al. Te impact of previous ovarian surgery on ovarian reserve in patients with endometriosis. BMC Womens Health. 2015; 15 (1): 74. Dunselman GA, Vermeulen N, Becker C, Calhaz-Jorge C, D’Hooghe T, De Bie B, et al. ESHRE guideline: management of women with endometriosis. Hum Reprod. 2014; 29 (3): 400–12. Allen C, Hopewell S, Prentice A. Non-steroidal anti-inflammatory drugs for pain in women with endometriosis. Cochrane Database Syst Rev. 2005; (4): CD004753. Marjoribanks J, Proctor ML, Farquhar C. Nonsteroidal anti-inflammatory drugs for primary dysmenorrhoea. Cochrane Database Syst Rev. 2003; (4): CD001751. Zito G, Luppi S, Giolo E, Martinelli M, Venturin I, Di Lorenzo G, et al. Medical treatments for endometriosis-associated pelvic pain. Biomed Res Int. 2014; 2014: 191967. Solomon DH. Patient information: Nonsteroidal antiinflammatory drugs (NSAIDs) (Beyond the Basics). Up to date. Dosegljivo 15.7.2015 s spletne strani: http://www.uptodate.com/contents/nonsteroidal-antiinflammatory-drugs-nsaids-beyond-the-basics. Soares SR, Martínez-Varea A, Hidalgo-Mora JJ, Pellicer A. Pharmacologic therapies in endometriosis: a systematic review. Fertil Steril. 2012; 98 (3): 529–55. Tarjanne S, Ng CH, Manconi F, Arola J, Mentula M, Maneck, et al. Use of hormonal therapy is associated with reduced nerve fber density in deep infltrating, rectovaginal endometriosis. Acta Obstet Gynecol Scand. 2015; 94 (7): 693–700. Wu L, Wu Q, Liu L. Oral contraceptive pills for endometriosis afer conservative surgery: a systematic review and meta-analysis. Gynecol Endocrinol. 2013; 29 (10): 883–90. Tu FF, Du H, Goldstein GP, Beaumont JL, Zhou Y, Brown WJ. Te influence of prior oral contraceptive use on risk of endometriosis is conditional on parity. Fertil Steril. 2014; 101 (6): 1697–704. Horne A, Critchley HOD. Medical therapies: progestines. In: Guidice LC, Evers JLH, Healy DL. Endometriosis: Science and Practice. New Delhi: Wily-Blackwell; 2007. p. 351–6. Andres MP, Lopes LA, Baracat EC, Podgaec S. Dienogest in the treatment of endometriosis: systematic review. Arch Gynecol Obstet. 2015 Sep; 292 (3): 523–9 Register zdravil. Dostopno 30.7.2015 s spletne strani: https://mediately.co/si. Carr B, Dmowski WP, O’Brien C, Jiang P, Burke J, Jimenez R, et al. Elagolix, an oral GnRH antagonist, versus subcutaneous depot medroxyprogesterone acetate for the treatment of endometriosis: effects on bone mineral density. Reprod Sci. 2014; 21 (11): 1341–51. Morotti M, Sozzi F, Remorgida V, Venturini PL, Ferrero S. Dienogest in women with persistent endometriosis-related pelvic pain during norethisterone acetate treatment. Eur J Obstet Gynecol Reprod Biol. 2014; 183: 188–92. Meldrum DR, Chang RJ, Lu J, Vale W, Rivier J, Judd HL. »Medical oophorectomy« using a long-acting GNRH agonist—a possible new approach to the treatment of endometriosis. J Clin Endocrinol Metab. 1982; 54 (5): 1081–3. Kumar P, Sharma A. Gonadotropin-releasing hormone analogs: Understanding advantages and limitations. J Hum Reprod Sci. 2014; 7 (3): 170–4. Khan KN, Kitajima M, Hiraki K, Fujishita A, Sekine I, Ishimaru T, et al. Changes in tissue inflammation, angiogenesis and apoptosis in endometriosis, adenomyosis and uterine myoma afer GnRH agonist therapy. Hum Reprod. 2010; 25 (3): 642–53. Surrey ES, Silverberg KM, Surrey MW, Schoolcraf WB. Effect of prolonged gonadotropin-releasing hormone agonist therapy on the outcome of in vitro fertilization-embryo transfer in patients with endometriosis. Fertil Steril. 2002; 78 (4): 699–704. Surrey ES, Hornstein MD. Prolonged GnRH agonist and add-back therapy for symptomatic endometriosis: long-term follow-up. Obstet Gynecol. 2002; 99 (5 Pt 1): 709–19. Brown J, Farquhar C. An overview of treatments for endometriosis. JAMA. 2015; 313 (3): 296–7. Selam B, Kayisli UA, Garcia-Velasco JA, Arici A. Extracellular matrix-dependent regulation of Fas ligand expression in human endometrial stromal cells. Biol Reprod. 2002; 66 (1): 1–5. Olivares CN, Bilotas MA, Ricci AG et al. Anastrozole and celecoxib for endometriosis treatment, good to keep them apart? Reproduction. 2013; 145 (2): 119–26. Matsuzaki S, Canis M, Pouly JL, Wattiez A, Okamura K, Mage G. Cyclooxygenase-2 expression in deep endometriosis and matched eutopic endometrium. Fertil Steril. 2004; 82 (5): 1309–15. Kim KH, Kim HY, Kim HH, Lee KS, Cheong J. Hypoxia induces expression of COX-2 through the homeodomain transcription factor CDX1 and orphan nuclear receptor SHP in human endometrial cells. Mol Hum Reprod. 2011; 17 (11): 710–9. Callejas NA, Fernández-Martínez A, Castrillo A, Boscá L, Martín-Sanz P. Selective inhibitors of cyclooxygenase-2 delay the activation of nuclear factor kappa B and attenuate the expression of inflammatory genes in murine macrophages treated with lipopolysaccharide. Mol Pharmacol. 2003; 63 (3): 671–7. Mattia C, Coluzzi F. COX-2 inhibitors: pharmacological data and adverse effects. Minerva Anestesiol. 2005; 71 (7–8): 461–70. Muñoz-Hernando L, Muñoz-Gonzalez JL, Marqueta-Marques L, Alvarez-Conejo C, Tejerizo-García Á, Lopez-Gonzalez G, et al. Endometriosis: alternative methods of medical treatment. Int J Womens Health. 2015; 7: 595–603. Rižner TL. Diagnostic potential of peritoneal fluid biomarkers of endometriosis. Expert Rev Mol Diagn. 2015; 15 (4): 557–80. Richter ON, Dorn C, Rösing B, Krebs D. Tumor necrosis factor alpha secretion by peritoneal macrophages in patients with endometriosis. Arch Gynecol Obstet. 2005; 271 (2): 143–7. Yildirim G, Attar R, Ficicioglu C, Karateke A, Ozkan F, Yesildaglar N. Etanercept causes regression of endometriotic implants in a rat model. Arch Gynecol Obstet. 2011; 283 (6): 1297–302. Koninckx PR, Craessaerts M, Timmerman D, Cornillie F, Kennedy S. Anti-TNF-alpha treatment for deep endometriosis-associated pain: a randomized placebo-controlled trial. Hum Reprod. 2008; 23 (9): 2017–2023. Quattrone F, Sanchez AM, Pannese M, Hemmerle T, Viganò P, Candiani M, et al. Te targeted delivery of interleukin 4 inhibits development of endometriotic lesions in a mouse model. Reprod Sci. 2015; 22 (9): 1143–52. Bulun SE, Attar E, Gurates B. Medial therapies: aromatase inhibitors. In: Guidice LC, Evers JLH, Healy DL. Endometriosis in science. New Delhi: Wiley-Blackwell; 2007. p. 357–365. Bulun SE, Sharda G, Rink J, Sharma S, Simpson ER. Distribution of aromatase P450 transcripts and adipose fbroblasts in the human breast. J Clin Endocrinol Metab. 1996; 81: 1273–1277. Pavone ME, Bulun SE. Aromatase inhibitors for the treatment of endometriosis. Fertil Steril. 2012; 98 (6): 1370–9. Kulak J Jr, Fischer C, Komm B, Taylor HS. Treatment with bazedoxifene, a selective estrogen receptor modulator, causes regression of endometriosis in a mouse model. Endocrinology. 2011; 152 (8): 3226–32. Shang Y. Molecular mechanisms of oestrogen and SERMs in endometrial carcinogenesis. Nat Rev Cancer. 2006; 6 (5): 360–8. Taylor HS, Osteen KG, Bruner-Tran KL, Lockwood CJ, Krikun G, Sokalska A, et al. Novel therapies targeting endometriosis. Reprod Sci. 2011; 18 (9): 814–23. Narvekar N, Cameron S, Critchley HO, Lin S, Cheng L, Baird DT. Low-dose mifepristone inhibits endometrial proliferation and up-regulates androgen receptor. J Clin Endocrinol Metab. 2004; 89 (5): 2491–7. Kettel LM, Murphy AA, Morales AJ, Yen SS. Preliminary report on the treatment of endometriosis with low-dose mifepristone (RU 486). Am J Obstet Gynecol. 1998; 178 (6): 1151–6. Broqua P, Riviere PJ, Conn PM, Rivier JE, Aubert ML, Junien JL. Pharmacological profle of a new, potent, and long-acting gonadotropin-releasing hormone antagonist: degarelix. J Pharmacol Exp Ter. 2002; 301 (1): 95–102. Ezzati M, Carr BR. Elagolix, a novel, orally bioavailable GnRH antagonist under investigation for the treatment of endometriosis-related pain. Womens Health (Lond Engl). 2015; 11 (1): 19–28. Diamond MP, Carr B, Dmowski WP, Koltun W, O’Brien C, Jiang P, et al. Elagolix treatment for endometriosis-associated pain: results from a phase 2, randomized, double-blind, placebo-controlled study. Reprod Sci. 2014; 21 (3): 363–71. Altintas D, Kokcu A, Tosun M, Cetinkaya MB, Kandemir B. Comparison of the effects of cetrorelix, a GnRH antagonist, and leuprolide, a GnRH agonist, on experimental endometriosis. J Obstet Gynaecol Res. 2008; 34 (6): 1014–9. Finas D, Hornung D, Diedrich K, Schultze-Mosgau A. Cetrorelix in the treatment of female infertility and endometriosis. Expert Opin Pharmacother. 2006; 7 (15): 2155–68. Depalo R, Jayakrishan K, Garruti G, Totaro I, Panzarino M, Giorgino F, et al. GnRH agonist versus GnRH antagonist in in vitro fertilization and embryo transfer (IVF/ET). Reprod Biol Endocrinol. 2012; 10: 26. Tarlatzis BC, Kolibianakis EM. GnRH agonists vs antagonists, Practice points, Research agenda. Bpobgyn. 2007; 21 (1): 57–65. Orvieto R, Patrizio P. GnRH agonist versus GnRH antagonist in ovarian stimulation: an ongoing debate. Reprod Biomed Online. 2013; 26 (1): 4–8. Ozer H, Boztosun A, Açmaz G, Atilgan R, Akkar OB, Kosar MI. Te efcacy of bevacizumab, sorafenib, and retinoic acid on rat endometriosis model. Reprod Sci. 2013; 20 (1): 26–32. Dahut WL, Lakhani NJ, Gulley JL, Arlen PM, Kohn EC, Kotz H, et al. Phase I clinical trial of oral 2-methoxyestradiol, an antiangiogenic and apoptotic agent, in patients with solid tumors. Cancer Biol Ter. 2006; 5 (1): 22–7. Becker CM, Rohwer N, Funakoshi T, Cramer T, Bernhardt W, Birsner A, et al. 2-methoxyestradiol inhibits hypoxia-inducible factor-1{alpha} and suppresses growth of lesions in a mouse model of endometriosis. Am J Pathol. 2008; 172 (2): 534–44. Ercan CM, Kayaalp O, Cengiz M, Keskin U, Yumusak N, Aydogan U, et al. Comparison of efcacy of bromocriptine and cabergoline to GnRH agonist in a rat endometriosis model. Arch Gynecol Obstet. 2015; 291 (5): 1103–11. Xin L, Hou Q, Xiong QI, Ding X. Association between matrix metalloproteinase-2 and matrix metalloproteinase-9 polymorphisms and endometriosis: A systematic review and meta-analysis. Biomed Rep. 2015; 3 (4): 559–565. Yang M, Jiang C, Chen H, Nian Y, Bai Z, Ha C. Te involvement of osteopontin and matrix metalloproteinase- 9 in the migration of endometrial epithelial cells in patients with endometriosis. Reprod Biol Endocrinol. 2015; 13 (1): 95. Almassinokiani F, Mehdizadeh A, Sariri E, Rezaei M, Almasi A, Akbari H, et al. Effects of simvastatin in prevention of pain recurrences afer surgery for endometriosis. Med Sci Monit. 2013; 19: 534–9. Cetinkaya N, Attar R, Yildirim G, Ficicioglu C, Ozkan F, Yilmaz B, et al. Te effects of different doses of melatonin treatment on endometrial implants in an oophorectomized rat endometriosis model. Arch Gynecol Obstet. 2015; 291 (3): 591–8. Schwertner A, Conceição Dos Santos CC, Costa GD, Deitos A, de Souza A, de Souza IC, et al. Efcacy of melatonin in the treatment of endometriosis: a phase II, randomized, double-blind, placebo-controlled trial. Pain. 2013; 154 (6): 874–81. Leconte M, Santulli P, Chouzenoux S, Marcellin L, Cerles O, Chapron C, et al. Inhibition of MAPK and VEGFR by sorafenib controls the progression of endometriosis. Reprod Sci. 2015. 2015; 22 (9): 1171–80. Zhang H, Xue J, Li M, Zhao X, Wei D, Li C. Metformin regulates stromal-epithelial cells communication via Wnt2/β-catenin signaling in endometriosis. Mol Cell Endocrinol. 2015; 413: 61–5 Zhou Y, Xu JN, Zeng C, Li X, Zhou YF, Qi Y, et al. Metformin Suppresses Prostaglandin E2-Induced Cytochrome P450 Aromatase Gene Expression and Activity via Stimulation of AMP-Activated Protein Kinase in Human Endometriotic Stromal Cells. Reprod Sci. 2015; 22 (9): 1162–70. Goumenou A, Panayiotides I, Matalliotakis I, Vlachonikolis I, Tzardi M, Koumantakis E. Bcl-2 and Bax expression in human endometriotic and adenomyotic tissues. Eur J Obstet Gynecol Reprod Biol. 2001; 99 (2): 256–60. Zhang Y, Cao H, Yu Z, Peng HY, Zhang CJ. Curcumin inhibits endometriosis endometrial cells by reducing estradiol production. Iran J Reprod Med. 2013; 11 (5): 415–22. Kim KH, Lee EN, Park JK, Lee JR, Lee JR, Kim JH, Choi HJ, et al. Curcumin attenuates TNF-α-induced expression of intercellular adhesion molecule-1, vascular cell adhesion molecule-1 and proinflammatory cytokines in human endometriotic stromal cells. Phytother Res. 2012; 26 (7): 1037–47. Jana S, Paul S, Swarnakar S. Curcumin as anti-endometriotic agent: implication of MMP-3 and intrinsic apoptotic pathway. Biochem Pharmacol. 2012; 83 (6): 797–804. Zhang Y, Cao H, Hu YY, Wang H, Zhang CJ. Inhibitory effect of curcumin on angiogenesis in ectopic endometrium of rats with experimental endometriosis. Int J Mol Med. 2011; 27 (1): 87–94. Nasu K, Nishida M, Ueda T, Takai N, Bing S, Narahara H, et al. Bufalin induces apoptosis and the G0/G1 cell cycle arrest of endometriotic stromal cells: a promising agent for the treatment of endometriosis. Mol Hum Reprod. 2005; 11 (11): 817–23. Nakaya K, Miyasaka T. A shikonin derivative, beta-hydroxyisovalerylshikonin, is an ATP-non-competitive inhibitor of protein tyrosine kinases. Anticancer Drugs. 2003; 14 (9): 683–93. Iwabuchi T, Yoshimoto C, Shigetomi H, Kobayashi H. Oxidative stress and antioxidant defense in endometriosis and its malignant transformation. Oxid Med Cell Longev. 2015; 2015: 848595. Harlev A, Gupta S, Agarwal A. Targeting oxidative stress to treat endometriosis. Expert Opin Ter Targets. 2015; 19 (11): 1447–64. Darling AM, Chavarro JE, Malspeis S, Harris HR, Missmer SA. A prospective cohort study of Vitamins B, C, E, and multivitamin intake and endometriosis. J Endometr. 2013; 5 (1): 17–26. Bhat KPL, Kosmeder JW 2nd, Pezzuto JM. Biological effects of resveratrol. Antioxid Redox Signal. 2001; 3 (6): 1041–64. Timmers S, Konings E, Bilet L, Houtkooper RH, van de Weijer T, Goossens GH, et al. Calorie restriction-like effects of 30 days of resveratrol supplementation on energy metabolism and metabolic profle in obese humans. Cell Metab. 2011 Nov 2; 14 (5): 612–22. Yavuz S, Aydin NE, Celik O, Houtkooper RH, van de Weijer T, Goossens GH, et al. Resveratrol successfully treats experimental endometriosis through modulation of oxidative stress and lipid peroxidation. J Cancer Res Ter. 2014; 10 (2): 324–9. Taguchi A, Wada-Hiraike O, Kawana K, Koga K, Yamashita A, Shirane A, et al. Resveratrol suppresses inflammatory responses in endometrial stromal cells derived from endometriosis: a possible role of the sirtuin 1 pathway. J Obstet Gynaecol Res. 2014; 40 (3): 770–8. Durak Y, Kokcu A, Kefeli M, Bildircin D, Çelik H, Alper T. Effect of vitamin C on the growth of experimentally induced endometriotic cysts. J Obstet Gynaecol Res. 2013; 39 (7): 1253–8. Mojzis J, Varinska L, Mojzisova G, Kostova I, Mirossay L. Antiangiogenic effects of flavonoids and chalcones. Pharmacol Res. 2008; 57 (4): 259–65. Matsuzaki S, Darcha C. Antifbrotic properties of epigallocatechin-3-gallate in endometriosis. Hum Reprod. 2014; 29 (8): 1677–87. Wang CC, Xu H, Man GC, Zhang T, Chu KO, Chu CY, et al. Prodrug of green tea epigallocatechin-3-gallate (Pro-EGCG) as a potent anti-angiogenesis agent for endometriosis in mice. Angiogenesis. 2013; 16 (1): 59–69. Zhou YX, Zhang H, Peng C. Puerarin: a review of pharmacological effects. Phytother Res. 2014; 28 (7): 961–75. Ji M, Liu Y, Yang S, Zhai D, Zhang D, Bai L, et al. Puerarin suppresses proliferation of endometriotic stromal cells in part via differential recruitment of nuclear receptor coregulators to estrogen receptor-α. J Steroid Biochem Mol Biol. 2013; 138: 421–6. Cheng W, Chen L, Yang S, Han J, Zhai D, Ni J, et al. Puerarin suppresses proliferation of endometriotic stromal cells partly via the MAPK signaling pathway induced by 17ß-estradiol-BSA. PLoS One. 2012; 7 (9): e45529. Chen Y, Chen C, Shi S, Han J, Wang J, Hu J, et al. Endometriotic implants regress in rat models treated with puerarin by decreasing estradiol level. Reprod Sci. 2011; 18 (9): 886–91. Nasu K, Kawano Y, Kai K, Aoyagi Y, Abe W, Okamoto M, et al. Aberrant histone modifcation in endometriosis. Front Biosci (Landmark Ed). 2014; 19: 1202–14. Samartzis EP, Noske A, Samartzis N, Fink D, Imesch P. Te expression of histone deacetylase 1, but not other class I histone deacetylases, is signifcantly increased in endometriosis. Reprod Sci. 2013; 20 (12): 1416–22. Lu Y, Nie J, Liu X, Zheng Y, Guo SW. Trichostatin A, a histone deacetylase inhibitor, reduces lesion growth and hyperalgesia in experimentally induced endometriosis in mice. Hum Reprod. 2010; 25 (4): 1014–25. Imesch P, Fink D, Fedier A. Romidepsin reduces histone deacetylase activity, induces acetylation of histones, inhibits proliferation, and activates apoptosis in immortalized epithelial endometriotic cells. Fertil Steril. 2010; 94 (7): 2838–42. Imesch P, Samartzis EP, Schneider M, Fink D, Fedier A. Inhibition of transcription, expression, and secretion of the vascular epithelial growth factor in human epithelial endometriotic cells by romidepsin. Fertil Steril. 2011; 95 (5): 1579-83. Downloads Published Issue Section License The Author transfers to the Publisher (Slovenian Medical Association) all economic copyrights following form Article 22 of the Slovene Copyright and Related Rights Act (ZASP), including the right of reproduction, the right of distribution, the rental right, the right of public performance, the right of public transmission, the right of public communication by means of phonograms and videograms, the right of public presentation, the right of broadcasting, the right of rebroadcasting, the right of secondary broadcasting, the right of communication to the public, the right of transformation, the right of audiovisual adaptation and all other rights of the author according to ZASP. 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