Interplay between Misplaced Müllerian-Derived Stem Cells and Peritoneal Immune Dysregulation in the Pathogenesis of Endometriosis

Antonio Simone Laganà, Emanuele Sturlese, Giovanni Retto, Vincenza Sofo, Onofrio Triolo, Antonio Simone Laganà, Emanuele Sturlese, Giovanni Retto, Vincenza Sofo, Onofrio Triolo

Abstract

In the genetic regulation of Müllerian structures development, a key role is played by Hoxa and Wnt clusters, because they lead the transcription of different genes according to the different phases of the organogenesis, addressing correctly cell-to-cell interactions, allowing, finally, the physiologic morphogenesis. Accumulating evidence is suggesting that dysregulation of Wnt and/or Hox genes may affect cell migration during organogenesis and differentiation of Müllerian structures of the female reproductive tract, with possible dislocation and dissemination of primordial endometrial stem cells in ectopic regions, which have high plasticity to differentiation. We hypothesize that during postpubertal age, under the influence of different stimuli, these misplaced and quiescent ectopic endometrial cells could acquire new phenotype, biological functions, and immunogenicity. So, these kinds of cells may differentiate, specializing in epithelium, glands, and stroma to form a functional ectopic endometrial tissue. This may provoke a breakdown in the peritoneal cavity homeostasis, with the consequent processes of immune alteration, documented by peripheral mononuclear cells recruitment and secretion of inflammatory cytokines in early phases and of angiogenic and fibrogenic cytokines in the late stages of the disease.

Figures

Figure 1
Figure 1
Hoxa and Wnt interplay mechanism. Hox—homeobox protein: this gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor that may regulate gene expression, morphogenesis, and differentiation. More specifically, it may function in fertility, embryo viability, and regulation of hematopoietic lineage commitment. Wnt—wingless-type: this gene is involved in the development of the anterior-posterior axis in the female reproductive tract and also plays a critical role in uterine smooth muscle pattering and maintenance of adult uterine function. BMP—bone morphogenetic protein: the protein encoded by this gene is a member of the bone morphogenetic protein family which is part of the transforming growth factor-beta superfamily. The superfamily includes large families of growth and differentiation factors. Please refer to chapters 5 (Role of Hoxa genes), 6 (Role of Wnt genes), and 7 (Hoxa and Wnt dynamic interplay) for extensive explanation.

References

    1. Giudice LC, Kao LC. Endometriosis. The Lancet. 2004;364(9447):1789–1799.
    1. Baldi A, Campioni M, Signorile PG. Endometriosis: pathogenesis, diagnosis, therapy and association with cancer. Oncology Reports. 2008;19(4):843–846.
    1. Bulun SE. Endometriosis. The New England Journal of Medicine. 2009;360(3):268–279.
    1. Fourquet J, Báez L, Figueroa M, Iriarte RI, Flores I. Quantification of the impact of endometriosis symptoms on health-related quality of life and work productivity. Fertility and Sterility. 2011;96(1):107–112.
    1. Jones G, Jenkinson C, Kennedy S. The impact of endometriosis upon quality of life: a qualitative analysis. Journal of Psychosomatic Obstetrics and Gynecology. 2004;25(2):123–133.
    1. Nnoaham KE, Hummelshoj L, Webster P, et al. Impact of endometriosis on quality of life and work productivity: a multicenter study across ten countries. Fertility and Sterility. 2011;96(2):366.e8–373.e8.
    1. Fanta M, Koliba P, Hrušková H. Endometriosis. Ceska Gynekol. 2012;77(4):314–319.
    1. Jia SZ, Leng JH, Shi JH, Sun PR, Lang JH. Health-related quality of life in women with endometriosis: a systematic review. Journal of Ovarian Research. 2012;5(1):p. 29.
    1. Gao X, Yeh Y-C, Outley J, Simon J, Botteman M, Spalding J. Health-related quality of life burden of women with endometriosis: a literature review. Current Medical Research and Opinion. 2006;22(9):1787–1797.
    1. Hemmings R, Rivard M, Olive DL, et al. Evaluation of risk factors associated with endometriosis. Fertility and Sterility. 2004;81(6):1513–1521.
    1. Eskenazi B, Warner ML. Epidemiology of endometriosis. Obstetrics and Gynecology Clinics of North America. 1997;24(2):235–258.
    1. Viganò P, Parazzini F, Somigliana E, Vercellini P. Endometriosis: epidemiology and aetiological factors. Best Practice and Research. 2004;18(2):177–200.
    1. Huhtinen K, Perheentupa A, Poutanen M, Heikinheimo O. Pathogenesis of endometriosis. Duodecim. 2011;127(17):1827–1835.
    1. Marana R, Lecca A, Biscione A, Muzii EL. Endometriosis: the gynecologist's opinion. Urologia. 2012;79(3):160–166.
    1. Stratton P, Berkley KJ. Chronic pelvic pain and endometriosis: translational evidence of the relationship and implications. Human Reproduction Update. 2011;17(3):327–346.
    1. Fauconnier A, Fritel X, Chapron C. Endometriosis and pelvic pain: epidemiological evidence of the relationship and implications. Gynecologie Obstetrique Fertilite. 2009;37(1):57–69.
    1. Porpora MG, Koninckx PR, Piazze J, Natili M, Colagrande S, Cosmi EV. Correlation between endometriosis and pelvic pain. Journal of the American Association of Gynecologic Laparoscopists. 1999;6(4):429–434.
    1. Vercellini P, Fedele L, Aimi G, Pietropaolo G, Consonni D, Crosignani PG. Association between endometriosis stage, lesion type, patient characteristics and severity of pelvic pain symptoms: a multivariate analysis of over 1000 patients. Human Reproduction. 2007;22(1):266–271.
    1. Arruda MS, Petta CA, Abrão MS, Benetti-Pinto CL. Time elapsed from onset of symptoms to diagnosis of endometriosis in a cohort study of Brazilian women. Human Reproduction. 2003;18(4):756–759.
    1. Berkley KJ, Rapkin AJ, Papka RE. The pains of endometriosis. Science. 2005;308(5728):1587–1589.
    1. Westney OL, Amundsen CL, Mcguire EJ. Bladder endometriosis: conservative management. Journal of Urology. 2000;163(6):1814–1817.
    1. Traşcă ET, Traşcă E, Tiţu A, Riza ML, Busuioc I. Ureteral stenosis due to endometriosis. Romanian Journal of Morphology and Embryology. 2012;53(2):433–437.
    1. Shook TE, Nyberg LM. Endometriosis of the urinary tract. Urology. 1988;31(1):1–6.
    1. Sinder C, Dochat GR, Wentsler NE. Splenoendometriosis. American Journal of Obstetrics and Gynecology. 1965;92:883–884.
    1. Saadat-Gilani K, Bechmann L, Frilling A, Gerken G, Canbay A. Gallbladder endometriosis as a cause of occult bleeding. World Journal of Gastroenterology. 2007;13(33):4517–4519.
    1. Kyamidis K, Lora V, Kanitakis J. Spontaneous cutaneous umbilical endometriosis: report of a new case with immunohistochemical study and literature review. Dermatology Online Journal. 2011;17(7):p. 5.
    1. American Society for Reproductive Medicine. Revised American society for reproductive medicine classification of endometriosis. Fertility and Sterility. 1997;67(5):817–821.
    1. Capobianco A, Rovere-Querini P. Endometriosis, a disease of the macrophage. Frontiers in Immunology. 2013;4, article 9
    1. Smith KA, Pearson CB, Hachey AM, Xia DL, Wachtman LM. Alternative activation of macrophages in rhesus macaques (Macaca mulatta) with endometriosis. Comparative Medicine. 2012;62(4):303–310.
    1. Mylonas KJ, Nair MG, Prieto-Lafuente L, Paape D, Allen JE. Alternatively activated macrophages elicited by helminth infection can be reprogrammed to enable microbial killing. Journal of Immunology. 2009;182(5):3084–3094.
    1. Arici A, Oral E, Attar E, Tazuke SI, Olive DL. Monocyte chemotactic protein-1 concentration in peritoneal fluid of women with endometriosis and its modulation of expression in mesothelial cells. Fertility and Sterility. 1997;67(6):1065–1072.
    1. Braun DP, Ding J, Shen J, Rana N, Fernandez BB, Dmowski WP. Relationship between apoptosis and the number of macrophages in eutopic endometrium from women with and without endometriosis. Fertility and Sterility. 2002;78(4):830–835.
    1. Cao X, Yang D, Song M, Murphy A, Parthasarathy S. The presence of endometrial cells in the peritoneal cavity enhances monocyte recruitment and induces inflammatory cytokines in mice: implications for endometriosis. Fertility and Sterility. 2004;82(supplement 3):999–1007.
    1. Pizzo A, Salmeri FM, Ardita FV, Sofo V, Tripepi M, Marsico S. Behaviour of cytokine levels in serum and peritoneal fluid of women with endometriosis. Gynecologic and Obstetric Investigation. 2002;54(2):82–87.
    1. Tariverdian N, Siedentopf F, Rücke M, et al. Intraperitoneal immune cell status in infertile women with and without endometriosis. Journal of Reproductive Immunology. 2009;80(1-2):80–90.
    1. Galleri L, Luisi S, Rotondi M, et al. Low serum and peritoneal fluid concentration of interferon-γ-induced protein-10 (CXCL10) in women with endometriosis. Fertility and Sterility. 2009;91(2):331–334.
    1. Lousse J-C, Defrère S, Van Langendonckt A, et al. Iron storage is significantly increased in peritoneal macrophages of endometriosis patients and correlates with iron overload in peritoneal fluid. Fertility and Sterility. 2009;91(5):1668–1675.
    1. Novembri R, Carrarelli P, Toti P, et al. Urocortin 2 and urocortin 3 inendometriosis: evidence for a possible role in inflammatory response. Molecular Human Reproduction. 2011;17(9):587–593.
    1. Chuang P-C, Wu M-H, Shoji Y, Tsai S-J. Downregulation of CD36 results in reduced phagocytic ability of peritoneal macrophages of women with endometriosis. The Journal of Pathology. 2009;219(2):232–241.
    1. Chuang P-C, Lin Y-J, Wu M-H, Wing L-YC, Shoji Y, Tsai S-J. Inhibition of CD36-dependent phagocytosis by prostaglandin E2 contributes to the development of endometriosis. The American Journal of Pathology. 2010;176(2):850–860.
    1. Bacci M, Capobianco A, Monno A, et al. Macrophages are alternatively activated in patients with endometriosis and required for growth and vascularization of lesions in a mouse model of disease. The American Journal of Pathology. 2009;175(2):547–556.
    1. Borda JT, Alvarez X, Mohan M, et al. CD163, a marker of perivascular macrophages, is up-regulated by microglia in simian immunodeficiency virus encephalitis after haptoglobin-hemoglobin complex stimulation and is suggestive of breakdown of the blood-brain barrier. The American Journal of Pathology. 2008;172(3):725–737.
    1. Cairo G, Recalcati S, Mantovani A, Locati M. Iron trafficking and metabolism in macrophages: contribution to the polarized phenotype. Trends in Immunology. 2011;32(6):241–247.
    1. Recalcati S, Locati M, Marini A, et al. Differential regulation of iron homeostasis during human macrophage polarized activation. European Journal of Immunology. 2010;40(3):824–835.
    1. Bach J-P, Rinn B, Meyer B, Dodel R, Bacher M. Role of MIF in inflammation and tumorigenesis. Oncology. 2008;75(3-4):127–133.
    1. Khoufache K, Bazin S, Girard K, et al. Macrophage migration inhibitory factor antagonist blocks the development of endometriosis in vivo. PLoS One. 2012;7(5)e37264
    1. Akoum A, Metz CN, Al-Akoum M, Kats R. Macrophage migration inhibitory factor expression in the intrauterine endometrium of women with endometriosis varies with disease stage, infertility status, and pelvic pain. Fertility and Sterility. 2006;85(5):1379–1385.
    1. Seeber B, Sammel MD, Fan X, et al. Panel of markers can accurately predict endometriosis in a subset of patients. Fertility and Sterility. 2008;89(5):1073–1081.
    1. Carli C, Metz CN, Al-Abed Y, Naccache PH, Akoum A. Up-regulation of cyclooxygenase-2 expression and prostaglandin E 2 production in human endometriotic cells by macrophage migration inhibitory factor: involvement of novel kinase signaling pathways. Endocrinology. 2009;150(7):3128–3137.
    1. Petrenko O, Fingerle-Rowson G, Peng T, Mitchell RA, Metz CN. Macrophage migration inhibitory factor deficiency is associated with altered cell growth and reduced susceptibility to Ras-mediated transformation. The Journal of Biological Chemistry. 2003;278(13):11078–11085.
    1. Nishihira J, Ishibashi T, Fukushima T, Sun B, Sato Y, Todo S. Macrophage migration inhibitory factor (MIF): Its potential role in tumor growth and tumor-associated angiogenesis. Annals of the New York Academy of Sciences. 2003;995:171–182.
    1. Bianco B, André GM, Vilarino FL, et al. The possible role of genetic variants in autoimmune-related genes in the development of endometriosis. Human Immunology. 2012;73(3):306–315.
    1. Treloar SA, Wicks J, Nyholt DR, et al. Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. American Journal of Human Genetics. 2005;77(3):365–376.
    1. Singh MN, Stringfellow HF, Taylor SE, et al. Elevated expression of CYP1A1 and γ-SYNUCLEIN in human ectopic (ovarian) endometriosis compared with eutopic endometrium. Molecular Human Reproduction. 2008;14(11):655–663.
    1. Wu C-H, Guo C-Y, Yang J-G, et al. Polymorphisms of dioxin receptor complex components and detoxification-related genes jointly confer susceptibility to advanced-stage endometriosis in the taiwanese han population. American Journal of Reproductive Immunology. 2012;67(2):160–168.
    1. Vichi S, Medda E, Ingelido AM, et al. Glutathione transferase polymorphisms and risk of endometriosis associated with polychlorinated biphenyls exposure in Italian women: a gene-environment interaction. Fertility and Sterility. 2012;97(5):1143.e3–1151.e3.
    1. Painter JN, Nyholt DR, Morris A, et al. High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19. Fertility and Sterility. 2011;95(7):2236–2240.
    1. Costa IR, Silva RCPC, Frare AB, et al. Polymorphism of the progesterone receptor gene associated with endometriosis in patients from Goiás, Brazil. Genetics and Molecular Research. 2011;10(3):1364–1370.
    1. Govatati S, Tangudu NK, Deenadayal M, Chakravarty B, Shivaji S, Bhanoori M. Association of E-cadherin single nucleotide polymorphisms with the increased risk of endometriosis in Indian women. Molecular Human Reproduction. 2012;18(5):280–287.
    1. Guo S-W. Association of endometriosis risk and genetic polymorphisms involving sex steroid biosynthesis and their receptors: a meta-analysis. Gynecologic and Obstetric Investigation. 2006;61(2):90–105.
    1. Kim H, Park JH, Ku S-Y, Kim SH, Choi YM, Kim JG. Association between endometriosis and polymorphisms in insulin-like growth factors (IGFs) and IGF-I receptor genes in Korean women. European Journal of Obstetrics Gynecology and Reproductive Biology. 2011;156(1):87–90.
    1. Kim H, Ku S-Y, Kim SH, Choi YM, Kim JG. Association between endometriosis and polymorphisms in insulin-like growth factor binding protein genes in Korean women. European Journal of Obstetrics Gynecology and Reproductive Biology. 2012;162(1):96–101.
    1. Çayan F, Ertun D, Aras-Ateş N, et al. Association of G1057D variant of insulin receptor substrate-2 with endometriosis. Fertility and Sterility. 2010;94(5):1622–1626.
    1. Ammendola M, Bottini N, Pietropolli A, Saccucci P, Gloria-Bottini F. Association between PTPN22 and endometriosis. Fertility and Sterility. 2008;89(4):993–994.
    1. Lee GH, Choi YM, Kim SH, et al. Interleukin-2 receptor β gene C627T polymorphism in Korean women with endometriosis: a case-control study. Human Reproduction. 2009;24(10):2596–2599.
    1. Gonçalves-Filho RP, Brandes A, Christofolini DM, Lerner TG, Bianco B, Barbosa CP. Plasminogen activator inhibitor-1 4G/5G polymorphism in infertile women with and without endometriosis. Acta Obstetricia et Gynecologica Scandinavica. 2011;90(5):473–477.
    1. André GM, Barbosa CP, Teles JS, Vilarino FL, Christofolini DM, Bianco B. Analysis of FOXP3 polymorphisms in infertile women with and without endometriosis. Fertility and Sterility. 2011;95(7):2223–2227.
    1. Barbosa CP, Teles JS, Lerner TG, et al. Genetic association study of polymorphisms FOXP3 and FCRL3 in women with endometriosis. Fertility and Sterility. 2012;97(5):1124–1128.
    1. Ruiz LA, Dutil J, Ruiz A, et al. Single-nucleotide polymorphisms in the lysyl oxidase-like protein 4 and complement component 3 genes are associated with increased risk for endometriosis and endometriosis-associated infertility. Fertility and Sterility. 2011;96(2):512–515.
    1. Medeiros F, Wang X, Araujo ARC, et al. HMGA gene rearrangement is a recurrent somatic alteration in polypoid endometriosis. Human Pathology. 2012;43(8):1243–1248.
    1. Nyholt DR, Low SK, Anderson CA, et al. Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics. 2012;44(12):1355–1359.
    1. Osuga Y, Koga K, Hirota Y, Hirata T, Yoshino O, Taketani Y. Lymphocytes in endometriosis. American Journal of Reproductive Immunology. 2011;65(1):1–10.
    1. Sturlese E, Salmeri FM, Retto G, et al. Dysregulation of the Fas/FasL system in mononuclear cells recovered from peritoneal fluid of women with endometriosis. Journal of Reproductive Immunology. 2011;92(1-2):74–81.
    1. Laganà AS, D’Ascola A, Salmeri FM, et al. mRNA expression of Foxp3 and RORc transcription factors and of IL-10 and IL-17A cytokines in ovarian endometrioma of women with endometriosis. Journal of Endometriosis. 2012;4(4):227–228.
    1. Laganà AS, Pizzo A, D’Ascola A, et al. mRNA expression of transcription factors and cytokines in immune cells of ovarian endometrioma from women with endometriosis. Reproductive Sciences. 2013;20(3, supplement):146–147.
    1. Kalu E, Sumar N, Giannopoulos T, et al. Cytokine profiles in serum and peritoneal fluid from infertile women with and without endometriosis. Journal of Obstetrics and Gynaecology Research. 2007;33(4):490–495.
    1. Zhou L, Chong MMW, Littman DR. Plasticity of CD4+ T Cell Lineage Differentiation. Immunity. 2009;30(5):646–655.
    1. Basta P, Majka M, Jozwicki W, et al. The frequency of CD25+CD4+ and FOXP3+ regulatory T cells in ectopic endometrium and ectopic decidua. Reproductive Biology and Endocrinology. 2010;8, article 116
    1. Polanczyk MJ, Hopke C, Vandenbark AA, Offner H. Treg suppressive activity involves estrogen-dependent expression of programmed death-1 (PD-1) International Immunology. 2007;19(3):337–343.
    1. Berbic M, Fraser IS. Regulatory T cells and other leukocytes in the pathogenesis of endometriosis. Journal of Reproductive Immunology. 2011;88(2):149–155.
    1. Hirata T, Osuga Y, Hamasaki K, et al. Interleukin (IL)-17A stimulates IL-8 secretion, cyclooxygensase-2 expression, and cell proliferation of endometriotic stromal cells. Endocrinology. 2008;149(3):1260–1267.
    1. Hirata T, Osuga Y, Takamura M, et al. Recruitment of CCR6-expressing Th17 cells by CCL 20 secreted from IL-1β-, TNF-α-, and IL-17A-stimulated endometriotic stromal cells. Endocrinology. 2010;151(11):5468–5476.
    1. Budiu RA, Diaconu I, Chrissluis R, Dricu A, Edwards RP, Vlad AM. A conditional mouse model for human MUC1-positive endometriosis shows the presence of anti-MUC1 antibodies and Foxp3+ regulatory T cells. Disease Models and Mechanisms. 2009;2(11-12):593–603.
    1. Podgaec S, Rizzo LV, Fernandes LF, Baracat EC, Abrao MS. CD4(+) CD25(high) Foxp3(+) cells increased in the peritoneal fluid of patients with endometriosis. American Journal of Reproductive Immunology. 2012;68(4):301–308.
    1. Oosterlynck DJ, Cornillie FJ, Waer M, Vandeputte M, Koninckx PR. Women with endometriosis show a defect in natural killer activity resulting in a decreased cytotoxicity to autologous endometrium. Fertility and Sterility. 1991;56(1):45–51.
    1. Sikora J, Mielczarek-Palacz A, Kondera-Anasz Z. Role of Natural Killer cell activity in the pathogenesis of endometriosis. Current Medicinal Chemistry. 2011;18(2):200–208.
    1. Agic A, Djalali S, Diedrich K, Hornung D. Apoptosis in endometriosis. Gynecologic and Obstetric Investigation. 2009;68(4):217–223.
    1. Harada T, Taniguchi F, Izawa M, et al. Apoptosis and endometriosis. Frontiers in Bioscience. 2007;12(8):3140–3151.
    1. Ulukus M, Arici A. Immunology of endometriosis. Minerva Ginecologica. 2005;57(3):237–248.
    1. Gregory CD, Pound JD. Microenvironmental influences of apoptosis in vivo and in vitro. Apoptosis. 2010;15(9):1029–1049.
    1. Tzifi F, Economopoulou C, Gourgiotis D, Ardavanis A, Papageorgiou S, Scorilas A. The role of BCL2 family of apoptosis regulator proteins in acute and chronic leukemias. Advances in Hematology. 2012;2012:15 pages.524308
    1. Peter ME, Budd RC, Desbarats J, et al. The CD95 receptor: apoptosis revisited. Cell. 2007;129(3):447–450.
    1. Strasser A, Jost PJ, Nagata S. The many roles of FAS receptor signaling in the immune system. Immunity. 2009;30(2):180–192.
    1. Lettau M, Paulsen M, Kabelitz D, Janssen O. FasL expression and reverse signalling. Results and Problems in Cell Differentiation. 2009;49:49–61.
    1. Suda T, Takahashi T, Golstein P, Nagata S. Molecular cloning and expression of the Fas ligand, a novel member of the tumor necrosis factor family. Cell. 1993;75(6):1169–1178.
    1. Lettau M, Paulsen M, Kabelitz D, Janssen O. Storage, expression and function of Fas ligand, the key death factor of immune cells. Current Medicinal Chemistry. 2008;15(17):1684–1696.
    1. O Reilly LA, Tai L, Lee L, et al. Membrane-bound Fas ligand only is essential for Fas-induced apoptosis. Nature. 2009;461(7264):659–663.
    1. Paunel-Görgülü A, Flohé S, Scholz M, Windolf J, Lögters T. Increased serum soluble Fas after major trauma is associated with delayed neutrophil apoptosis and development of sepsis. Critical Care. 2011;15(1):p. R20.
    1. Weinlich R, Brunner T, Amarante-Mendes GP. Control of death receptor ligand activity by posttranslational modifications. Cellular and Molecular Life Sciences. 2010;67(10):1631–1642.
    1. Cabal-Hierro L, Lazo PS. Signal transduction by tumor necrosis factor receptors. Cellular Signalling. 2012;24(6):1297–1305.
    1. Laganà AS, Salmeri FM, Retto G, et al. Stage-related changes of peritoneal soluble TNFαand TNFR1 and TNFR2 in cells recovered from PF of women with endometriosis. Journal of Reproductive Immunology. 2012;94(1):94–95.
    1. Zhao ZZ, Nyholt DR, Le L, et al. Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample. Human Reproduction. 2007;22(9):2389–2397.
    1. Chae SJ, Kim H, Jee BC, Suh CS, Kim SH, Kim JG. Tumor necrosis factor (TNF)-TNF receptor gene polymorphisms and their serum levels in Korean women with endometriosis. American Journal of Reproductive Immunology. 2008;60(5):432–439.
    1. Vijaya Lakshmi K, Shetty P, Vottam K, Govindhan S, Ahmad SN, Hasan Q. Tumor necrosis factor alpha -C850T polymorphism is significantly associated with endometriosis in Asian Indian women. Fertility and Sterility. 2010;94(2):453–456.
    1. Paul Dmowski W, Braun DP. Immunology of endometriosis. Best Practice & Research Clinical Obstetrics & Gynaecology. 2004;18(2):245–263.
    1. Trovó de Marqui AB. Genetic polymorphisms and endometriosis: contribution of genes that regulate vascular function and tissue remodeling. Revista da Associação Médica Brasileira. 2012;58(5):620–632.
    1. Khoufache K, Bondza PK, Harir N, et al. Soluble human IL-1 receptor type 2 inhibits ectopic endometrial tissue implantation and growth: identification of a novel potential target for endometriosis treatment. The American Journal of Pathology. 2012;181(4):1197–1205.
    1. Sikora J, Mielczarek-Palacz A, Kondera-Anasz Z. Imbalance in cytokines from interleukin-1 family—role in pathogenesis of endometriosis. American Journal of Reproductive Immunology. 2012;68(2):138–45.
    1. Bersinger NA, Dechaud H, McKinnon B, Mueller MD. Analysis of cytokinesin the peritoneal fluid of endometriosispatients as a function of the menstrual cycle stage using the Bio-Plex platform. Archives of Physiology and Biochemistry. 2012;118(4):210–218.
    1. Wickiewicz D, Chrobak A, Gmyrek GB, et al. Diagnostic accuracy of interleukin-6 levels in peritoneal fluid for detection of endometriosis. Archives of Gynecology and Obstetrics. 2013
    1. Carmona F, Chapron C, Martínez-Zamora MÁ, et al. Ovarian endometrioma but not deep infiltrating endometriosis is associated with increased serum levels of interleukin-8 and interleukin-6. Journal of Reproductive Immunology. 2012;95(1-2):80–86.
    1. Fan W, Li S, Chen Q, Huang Z, Ma Q, Xiao Z. Association between interleukin-10 promoter polymorphisms and endometriosis: a meta-analysis. Gene. 2013;515(1):49–55.
    1. Arici A, Matalliotakis I, Goumenou A, et al. Increased levels of interleukin-15 in the peritoneal fluid of women with endometriosis: inverse correlation with stage and depth of invasion. Human Reproduction. 2003;18(2):429–432.
    1. Zhang F, Yang Y, Wang Y. Association between TGF-β1-509C/T polymorphism and endometriosis: a systematic review and meta-analysis. European Journal of Obstetrics & Gynecology and Reproductive Biology. 2012;164(2):121–126.
    1. Arici A, Matalliotakis I, Goumenou A, Koumantakis G, Vassiliadis S, Mahutte NG. Altered expression of interleukin-18 in the peritoneal fluid of women with endometriosis. Fertility and Sterility. 2003;80(4):889–894.
    1. Santulli P, Borghese B, Chouzenoux S, et al. Interleukin-19 and interleukin-22 serum levels are decreased in patients with ovarian endometrioma. Fertility and Sterility. 2013;99(1):219–226.
    1. Santulli P, Borghese B, Chouzenoux S, et al. Serum and peritoneal interleukin-33 levels are elevated in deeply infiltrating endometriosis. Human Reproduction. 2012;27(7):2001–2009.
    1. Wu MY, Ho HN. The role of cytokines in endometriosis. American Journal of Reproductive Immunology. 2003;49(5):285–296.
    1. D’Hooghe TM, Nugent NP, Cuneo S, et al. Recombinant human TNFRSF1A (r-hTBP1) inhibits the development of endometriosis in baboons: a prospective, randomized, placebo- and drug-controlled study. Biology of Reproduction. 2006;74(1):131–136.
    1. Falconer H, Mwenda JM, Chai DC, et al. Treatment with anti-TNF monoclonal antibody (c5N) reduces the extent of induced endometriosis in the baboon. Human Reproduction. 2006;21(7):1856–1862.
    1. Harada T, Enatsu A, Mitsunari M, et al. Role of cytokines in progression of endometriosis. Gynecologic and Obstetric Investigation. 1999;47(supplement 1):34–40.
    1. Braundmeier AG, Nowak RA. Cytokines regulate matrix metalloproteinases in human uterine endometrial fibroblast cells through a mechanism that does not involve increases in extracellular matrix metalloproteinase inducer. American Journal of Reproductive Immunology. 2006;56(3):201–214.
    1. Bruner-Tran KL, Eisenberg E, Yeaman GR, Anderson TA, McBean J, Osteen KG. Steroid and cytokine regulation of matrix metalloproteinase expression in endometriosis and the establishment of experimental endometriosis in nude mice. Journal of Clinical Endocrinology and Metabolism. 2002;87(10):4782–4791.
    1. Donnez J, Smoes P, Gillerot S, Casanas-Roux F, Nisolle M. Vascular endothelial growth factor (VEGF) in endometriosis. Human Reproduction. 1998;13(6):1686–1690.
    1. Fasciani A, D’Ambrogio G, Bocci G, Monti M, Genazzani AR, Artini PG. High concentrations of the vascular endothelial growth factor and interleukin-8 in ovarian endometriomata. Molecular Human Reproduction. 2000;6(1):50–54.
    1. McLaren J, Prentice A, Charnock-Jones DS, Smith SK. Vascular endothelial growth factor (VEGF) concentrations are elevated in peritoneal fluid of women with endometriosis. Human Reproduction. 1996;11(1):220–223.
    1. Takehara M, Ueda M, Yamashita Y, Terai Y, Hung Y-C, Ueki M. Vascular endothelial growth factor A and C gene expression in endometriosis. Human Pathology. 2004;35(11):1369–1375.
    1. Girling JE, Rogers PAW. Recent advances in endometrial angiogenesis research. Angiogenesis. 2005;8(2):89–99.
    1. Gilabert-Estellés J, Ramón LA, España F, et al. Expression of angiogenic factors in endometriosis: relationship to fibrinolytic and metalloproteinase systems. Human Reproduction. 2007;22(8):2120–2127.
    1. Braza-Boïls A, Gilabert-Estellés J, Ramón LA, et al. Peritoneal fluid reduces angiogenesis-related MicroRNA expression in cell cultures of endometrial and endometriotic tissues from women with endometriosis. PLoS One. 2013;8(4)e62370
    1. Barcz E, Milewski Ł, Dziunycz P, Kamiński P, Płoski R, Malejczyk J. Peritoneal cytokines and adhesion formation in endometriosis: an inverse association with vascular endothelial growth factor concentration. Fertility and Sterility. 2012;97(6):1380.e1–1386.e1.
    1. Cosín R, Gilabert-Estellés J, Ramón LA, et al. Vascular endothelial growth factor polymorphisms (-460C/T, +405G/C, and 936C/T) and endometriosis: their influence on vascular endothelial growth factor expression. Fertility and Sterility. 2009;92(4):1214–1220.
    1. Emamifar B, Salehi Z, Mehrafza M, Mashayekhi F. The vascular endothelial growth factor (VEGF) polymorphisms and the risk of endometriosis in northern Iran. Gynecological Endocrinology. 2012;28(6):447–450.
    1. Kim J-H, Yang Y-I, Ahn J-H, Lee J-G, Lee K-T, Choi J-H. Deer (Cervus elaphus) antler extract suppresses adhesion and migration of endometriotic cells and regulates MMP-2 and MMP-9 expression. Journal of Ethnopharmacology. 2012;140(2):391–397.
    1. Osteen KG, Yeaman GR, Bruner-Tran KL. Matrix metalloproteinases and endometriosis. Seminars in Reproductive Medicine. 2003;21(2):155–164.
    1. Shaco-Levy R, Sharabi S, Piura B, Sion-Vardy N. MMP-2, TIMP-1, E-cadherin, and β;-catenin expression in endometrial serous carcinoma compared with low-grade endometrial endometrioid carcinoma and proliferative endometrium. Acta Obstetricia et Gynecologica Scandinavica. 2008;87(8):868–874.
    1. Kim K-H, Lee EN, Park JK, 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. Phytotherapy Research. 2012;26(7):1037–1047.
    1. Berkkanoglu M, Arici A. Immunology and endometriosis. American Journal of Reproductive Immunology. 2003;50(1):48–59.
    1. Vigano P, Magri B, Busacca M, Vignali M, Pardi R, Di Blasio AM. Expression of intercellular adhesion molecule-1 (ICAM-1) on cultured human endometrial stromal cells and its role in the interaction with natural killers. American Journal of Reproductive Immunology. 1994;32(3):139–145.
    1. Defrère S, Donnez J, Moulin P, et al. Expression of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 in human endometrial stromal and epithelial cells is regulated by interferon-gamma but not iron. Gynecologic and Obstetric Investigation. 2008;65(3):145–154.
    1. Viganò P, Somigliana E, Gaffuri B, Santorsola R, Busacca M, Vignali M. Endometrial release of soluble intercellular adhesion molecule 1 and endometriosis: relationship to the extent of the disease. Obstetrics and Gynecology. 2000;95(1):115–118.
    1. Kyama CM, Overbergh L, Mihalyi A, et al. Endometrial and peritoneal expression of aromatase, cytokines, and adhesion factors in women with endometriosis. Fertility and Sterility. 2008;89(2):301–310.
    1. Wu MH, Chuang PC, Lin YJ, Tsai SJ. Suppression of annexin A2 by prostaglandin E2 impairs phagocytic ability of peritoneal macrophages in women with endometriosis. Human Reproduction. 2013;28(4):1045–1053.
    1. Maia H, Jr., Haddad C, Coelho G, Casoy J. Role of inflammation and aromatase expression in the eutopic endometrium and its relationship with the development of endometriosis. Womens Health. 2012;8(6):647–658.
    1. Bulun SE, Cheng Y-H, Pavone ME, et al. 17β-Hydroxysteroid dehydrogenase-2 deficiency and progesterone resistance in endometriosis. Seminars in Reproductive Medicine. 2010;28(1):44–50.
    1. Cheng Y-H, Imir A, Fenkci V, Yilmaz MB, Bulun SE. Stromal cells of endometriosis fail to produce paracrine factors that induce epithelial 17β-hydroxysteroid dehydrogenase type 2 gene and its transcriptional regulator Sp1: a mechanism for defective estradiol metabolism. American Journal of Obstetrics and Gynecology. 2007;196(4):391.e1–398.e1.
    1. Machado-Linde F, Pelegrin P, Sanchez-Ferrer ML, Leon J, Cascales P, Parrilla JJ. 2-methoxyestradiol in the pathophysiology of endometriosis: focus on angiogenesis and therapeutic potential. Reproductive Sciences. 2012;19(10):1018–1029.
    1. Missmer SA, Hankinson SE, Spiegelman D, et al. Reproductive history and endometriosis among premenopausal women. Obstetrics and Gynecology. 2004;104(5):965–974.
    1. Cumiskey J, Whyte P, Kelehan P, Gibbons D. A detailed morphologic and immunohistochemical comparison of pre- and postmenopausal endometriosis. Journal of Clinical Pathology. 2008;61(4):455–459.
    1. Parente Barbosa C, Bentes De Souza AM, Bianco B, Christofolini DM. The effect of hormones on endometriosis development. Minerva Ginecologica. 2011;63(4):375–386.
    1. Pabona JMP, Simmen FA, Nikiforov MA, et al. Krüppel-like factor 9 and progesterone receptor coregulation of decidualizing endometrial stromal cells: implications for the pathogenesis of endometriosis. Journal of Clinical Endocrinology and Metabolism. 2012;97(3):E376–E392.
    1. Vinatier D, Orazi G, Cosson M, Dufour P. Theories of endometriosis. European Journal of Obstetrics Gynecology and Reproductive Biology. 2001;96(1):21–34.
    1. Andrade SS, Azevedo AD, Monasterio IC, et al. 17β-Estradiol and steady-state concentrations of H2O2: antiapoptotic effect in endometrial cells from patients with endometriosis. Free Radical Biology & Medicine. 2013;60:63–72.
    1. Di W, Guo SW. The search for genetic variants predisposing women to endometriosis. Current Opinion in Obstetrics and Gynecology. 2007;19(4):395–401.
    1. Fan W, Li S, Chen Q, Huang Z, Ma Q, Xiao Z. Association between interleukin-10 promoter polymorphisms and endometriosis: a meta-analysis. Gene. 2013;515(1):49–55.
    1. Kashima K, Ishimaru T, Okamura H, et al. Familial risk among Japanese patients with endometriosis. International Journal of Gynecology and Obstetrics. 2004;84(1):61–64.
    1. Kennedy S, Mardon H, Barlow D. Familial endometriosis. Journal of Assisted Reproduction and Genetics. 1995;12(1):32–34.
    1. Hirschhorn JN, Lohmueller K, Byrne E, Hirschhorn K. A comprehensive review of genetic association studies. Genetics in Medicine. 2002;4(2):45–61.
    1. McCarty CA, Berg RL, Welter JD, Kitchner TE, Kemnitz JW. A novel gene-environment interaction involved in endometriosis. International Journal of Gynecology and Obstetrics. 2012;116(1):61–63.
    1. Ballester M, Dehan P, Béliard A, Brichant G, Nisolle M. Role of genetic and environmental factors in the development of endometriosis. Revue Médicale de Liège. 2012;67(5-6):374–380.
    1. Rahmioglu N, Missmer SA, Montgomery GW, Zondervan KT. Insights into assessing the genetics of endometriosis. Current Obstetrics and Gynecology Reports. 2012;1(3):124–137.
    1. Falconer H, D’Hooghe T, Fried G. Endometriosis and genetic polymorphisms. Obstetrical and Gynecological Survey. 2007;62(9):616–628.
    1. Zhao X, Zong L-L, Wang Y-F, et al. Association of single nucleotide polymorphism in CYP17 and ERα genes with endometriosis risk in southern Chinese women. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011;28(3):304–307.
    1. Vainio S, Heikkilä M, Kispert A, Chin N, McMahon AP. Female development in mammals is regulated by Wnt-4 signalling. Nature. 1999;397(6718):405–409.
    1. Guo X, Jing C, Li L, et al. Down-regulation of VEZT gene expression in human gastric cancer involves promoter methylation and miR-43c. Biochemical and Biophysical Research Communications. 2011;404(2):622–627.
    1. Boyer A, Lapointe É, Zheng X, et al. WNT4 is required for normal ovarian follicle development and female fertility. FASEB Journal. 2010;24(8):3010–3025.
    1. Rae JM, Johnson MD, Scheys JO, Cordero KE, Larios JM, Lippman ME. GREB1 is a critical regulator of hormone dependent breast cancer growth. Breast Cancer Research and Treatment. 2005;92(2):141–149.
    1. Acién P, Acién M, Sánchez-Ferrer M. Complex malformations of the female genital tract. New types and revision of classification. Human Reproduction. 2004;19(10):2377–2384.
    1. Morcel K, Guerrier D, Watrin T, Pellerin I, Levêque J. The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: clinical description and genetics. Journal de Gynecologie Obstetrique et Biologie de la Reproduction. 2008;37(6):539–546.
    1. Zanatta A, Rocha AM, Carvalho FM, et al. The role of the Hoxa10/HOXA10 gene in the etiology of endometriosis and its related infertility: a review. Journal of Assisted Reproduction and Genetics. 2010;27(12):701–710.
    1. Krumlauf R. Hox genes in vertebrate development. Cell. 1994;78(2):191–201.
    1. Taylor HS, Vanden Heuvel GB, Igarashi P. A conserved Hox axis in the mouse and human female reproductive system: late establishment and persistent adult expression of the Hoxa cluster genes. Biology of Reproduction. 1997;57(6):1338–1345.
    1. Modi D, Godbole G. HOXA10 signals on the highway through pregnancy. Journal of Reproductive Immunology. 2009;83(1-2):72–78.
    1. Lim H, Ma L, Ma W-G, Maas RL, Dey SK. Hoxa-10 regulates uterine stromal cell responsiveness to progesterone during implantation and decidualization in the mouse. Molecular Endocrinology. 1999;13(6):1005–1017.
    1. Painter JN, Anderson CA, Nyholt DR, et al. Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics. 2011;43(1):51–54.
    1. Cheng W, Liu J, Yoshida H, Rosen D, Naora H. Lineage infidelity of epithelial ovarian cancers is controlled by HOX genes that specify regional identity in the reproductive tract. Nature Medicine. 2005;11(5):531–537.
    1. Borghese B, Vaiman D, de Ziegler D, Chapron C. Endometriosis and genetics: what responsibility for the genes? Journal de Gynecologie Obstetrique et Biologie de la Reproduction. 2010;39(3):196–207.
    1. Daftary GS, Taylor HS. EMX2 gene expression in the female reproductive tract and aberrant expression in the endometrium of patients with endometriosis. Journal of Clinical Endocrinology and Metabolism. 2004;89(5):2390–2396.
    1. Lin J, Zong L, Kennedy SH, Zondervan KT. Coding regions of INHBA, SFRP4 and HOXA10 are not implicated in familial endometriosis linked to chromosome 7p13-15. Molecular Human Reproduction. 2011;17(10):605–611.
    1. Biason-Lauber A, Konrad D, Navratil F, Schoenle EJ. A WNT4 mutation associated with Müllerian-Duct regression and virilization in a 46,XX woman. The New England Journal of Medicine. 2004;351(8):792–798.
    1. Biason-Lauber A, De Filippo G, Konrad D, Scarano G, Nazzaro A, Schoenle EJ. WNT4 deficiency-a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. Human Reproduction. 2007;22(1):224–229.
    1. Hayashi K, Erikson DW, Tilford SA, et al. Wnt genes in the mouse uterus: potential regulation of implantation. Biology of Reproduction. 2009;80(5):989–1000.
    1. Sonderegger S, Pollheimer J, Knöfler M. Wnt signalling in implantation, decidualisation and placental differentiation—review. Placenta. 2010;31(10):839–847.
    1. Matsuzaki S, Darcha C, Maleysson E, Canis M, Mage G. Impaired down-regulation of E-cadherin and β-catenin protein expression in endometrial epithelial cells in the mid-secretory endometrium of infertile patients with endometriosis. Journal of Clinical Endocrinology and Metabolism. 2010;95(7):3437–3445.
    1. Bondos S. Variations on a theme: Hox and Wnt combinatorial regulation during animal development. Science’s STKE. 2006;2006(355):p. pe38.
    1. Klapholz-Brown Z, Walmsley GG, Nusse YM, Nusse R, Brown PO. Transcriptional program induced by Wnt protein in human fibroblasts suggests mechanisms for cell cooperativity in defining tissue microenvironments. PLoS One. 2007;2(9, article e945)
    1. Deschamps J. Ancestral and recently recruited global control of the Hox genes in development. Current Opinion in Genetics and Development. 2007;17(5):422–427.
    1. Cervelló I, Gil-Sanchis C, Mas A, et al. Human endometrial side population cells exhibit genotypic, phenotypic and functional features of somatic stem cells. PLoS One. 2010;5(6)e10964
    1. Tsuji S, Yoshimoto M, Takahashi K, Noda Y, Nakahata T, Heike T. Side population cells contribute to the genesis of human endometrium. Fertility and Sterility. 2008;90(4, supplement):1528–1537.
    1. Bratincsák A, Brownstein MJ, Cassiani-Ingoni R, et al. CD45-positive blood cells give rise to uterine epithelial cells in mice. Stem Cells. 2007;25(11):2820–2826.
    1. Masuda H, Matsuzaki Y, Hiratsu E, et al. Stem cell-like properties of the endometrial side population: implication in endometrial regeneration. PLoS One. 2010;5(4)e10387
    1. Ye L, Mayberry R, Lo CY, et al. Generation of human female reproductive tract epithelium from human embryonic stem cells. PLoS One. 2011;6(6)e21136
    1. Schwab KE, Chan RWS, Gargett CE. Putative stem cell activity of human endometrial epithelial and stromal cells during the menstrual cycle. Fertility and Sterility. 2005;84(supplement 2):1124–1130.
    1. Ikoma T, Kyo S, Maida Y, et al. Bone marrow-derived cells from male donors can compose endometrial glands in female transplant recipients. American Journal of Obstetrics and Gynecology. 2009;201(6):608.e1–608.e8.
    1. Taylor HS. Endometrial cells derived from donor stem cells in bone marrow transplant recipients. Journal of the American Medical Association. 2004;292(1):81–85.
    1. Gargett CE, Masuda H. Adult stem cells in the endometrium. Molecular Human Reproduction. 2010;16(11):818–834.
    1. Maruyama T, Masuda H, Ono M, Kajitani T, Yoshimura Y. Human uterine stem/progenitor cells: their possible role in uterine physiology and pathology. Reproduction. 2010;140(1):11–22.
    1. Sampson JA. Peritoneal endometriosis due to menstrual dissemination of endometrial tissue into the peritoneal cavity. American Journal of Obstetrics & Gynecology. 1927;14:442–469.
    1. Khan KN, Kitajima M, Hiraki K, et al. Immunopathogenesis of pelvic endometriosis: role of hepatocyte growth factor, macrophages and ovarian steroids. American Journal of Reproductive Immunology. 2008;60(5):383–404.
    1. Bellelis P, Dias JA, Jr., Podgaec S, Gonzales M, Baracat EC, Abrão MS. Epidemiological and clinical aspects of pelvic endometriosis—series of cases. Revista da Associacao Medica Brasileira. 2010;56(4):467–471.
    1. Anger DL, Foster WG. The link between environmental toxicant exposure and endometriosis. Frontiers in Bioscience. 2008;13(4):1578–1593.
    1. Ichida M, Gomi A, Hiranouchi N, et al. A case of cerebral endometriosis causing catamenial epilepsy. Neurology. 1993;43(12):2708–2709.
    1. Laghzaoui O, Laghzaoui M. Nasal endometriosis: apropos of 1 case. Journal de Gynecologie Obstetrique et Biologie de la Reproduction. 2001;30(8):786–788.
    1. Barresi V, Cerasoli S, Vitarelli E, Donati R. Spinal intradural müllerianosis: a case report. Histology and Histopathology. 2006;21(10–12):1111–1114.
    1. Sepilian V, Della Badia C. Iatrogenic endometriosis caused by uterine morcellation during a supracervical hysterectomy. Obstetrics and Gynecology. 2003;102(5):1125–1127.
    1. Signorile PG, Baldi F, Bussani R, D’Armiento M, De Falco M, Baldi A. Ectopic endometrium in human foetuses is a common event and sustains the theory of müllerianosis in the pathogenesis of endometriosis, a disease that predisposes to cancer. Journal of Experimental and Clinical Cancer Research. 2009;28(1, article 49)
    1. Signorile PG, Baldi F, Bussani R, et al. New evidence of the presence of endometriosis in the human fetus. Reproductive BioMedicine Online. 2010;21(1):142–147.
    1. Signorile PG, Baldi F, Bussani R, et al. Embryologic origin of endometriosis: analysis of 101 human female fetuses. Journal of Cellular Physiology. 2012;227(4):1653–1656.

Source: PubMed

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