User menu

Targeting mast cells: a new way to treat endometriosis

Bibliographic reference Binda, Maria Mercedes ; Donnez, Jacques ; Dolmans, Marie-Madeleine. Targeting mast cells: a new way to treat endometriosis. In: Expert Opinion On Therapeutic Targets, Vol. 21, no.1, p. 67-75 (2016)
Permanent URL http://hdl.handle.net/2078.1/180166
  1. Donnez Jacques, Peritoneal endometriosis is an inflammatory disease, 10.2741/e358
  2. Dunselman G. A. J., Vermeulen N., Becker C., Calhaz-Jorge C., D'Hooghe T., De Bie B., Heikinheimo O., Horne A. W., Kiesel L., Nap A., Prentice A., Saridogan E., Soriano D., Nelen W., ESHRE guideline: management of women with endometriosis, 10.1093/humrep/det457
  3. Donnez J, Panminerva Med (2016)
  4. Koninckx Philippe R., Ussia Anastasia, Adamyan Leila, Wattiez Arnaud, Donnez Jacques, Deep endometriosis: definition, diagnosis, and treatment, 10.1016/j.fertnstert.2012.07.1061
  5. Donnez Jacques, Lousse Jean-Christophe, Jadoul Pascale, Donnez Olivier, Squifflet Jean, Laparoscopic management of endometriomas using a combined technique of excisional (cystectomy) and ablative surgery, 10.1016/j.fertnstert.2009.02.065
  6. Jadoul Pascale, Kitajima Michio, Donnez Olivier, Squifflet Jean, Donnez Jacques, Surgical treatment of ovarian endometriomas: state of the art?, 10.1016/j.fertnstert.2012.06.023
  7. Berlanda Nicola, Somigliana Edgardo, Viganò Paola, Vercellini Paolo, Safety of medical treatments for endometriosis, 10.1517/14740338.2016.1121991
  8. Vercellini Paolo, Viganò Paola, Somigliana Edgardo, Fedele Luigi, Endometriosis: pathogenesis and treatment, 10.1038/nrendo.2013.255
  9. Nisolle Michelle, Donnez Jacques, Peritoneal endometriosis, ovarian endometriosis, and adenomyotic nodules of the rectovaginal septum are three different entities, 10.1016/s0015-0282(97)00191-x
  10. Sampson JA, Am J Pathol, 3, 93 (1927)
  11. Oral E, The peritoneal environment in endometriosis, 10.1093/humupd/2.5.385
  12. Maybin Jacqueline A., Critchley Hilary O.D., Jabbour Henry N., Inflammatory pathways in endometrial disorders, 10.1016/j.mce.2010.08.006
  13. Berbic M., Fraser I.S., Regulatory T cells and other leukocytes in the pathogenesis of endometriosis, 10.1016/j.jri.2010.11.004
  14. Berbic M., Schulke L., Markham R., Tokushige N., Russell P., Fraser I. S., Macrophage expression in endometrium of women with and without endometriosis, 10.1093/humrep/den393
  15. BARRIER BRETON F., Immunology of Endometriosis : , 10.1097/grf.0b013e3181db7c33
  16. Van Langendonckt Anne, Casanas-Roux Françoise, Donnez Jacques, Oxidative stress and peritoneal endometriosis, 10.1016/s0015-0282(02)02959-x
  17. Defrere S., Lousse J.C., Gonzalez-Ramos R., Colette S., Donnez J., Van Langendonckt A., Potential involvement of iron in the pathogenesis of peritoneal endometriosis, 10.1093/molehr/gan033
  18. Pirdel L., Pirdel M., Role of iron overload-induced macrophage apoptosis in the pathogenesis of peritoneal endometriosis, 10.1530/rep-13-0552
  19. Lousse Jean-Christophe, Defrère Sylvie, Van Langendonckt Anne, Gras Jérémie, González-Ramos Reinaldo, Colette Sébastien, Donnez Jacques, Iron storage is significantly increased in peritoneal macrophages of endometriosis patients and correlates with iron overload in peritoneal fluid, 10.1016/j.fertnstert.2008.02.103
  20. Santulli Pietro, Chouzenoux Sandrine, Fiorese Mauro, Marcellin Louis, Lemarechal Herve, Millischer Anne-Elodie, Batteux Frédéric, Borderie Didier, Chapron Charles, Protein oxidative stress markers in peritoneal fluids of women with deep infiltrating endometriosis are increased, 10.1093/humrep/deu290
  21. D?Cruz Osmond J., Uckun Fatih M., Targeting Mast Cells in Endometriosis with Janus Kinase 3 Inhibitor, JANEX-1, 10.1111/j.1600-0897.2007.00502.x
  22. Oosterlynck Didier J., Meuleman Christel, Waer Mark, Vandeputte Michel, Koninckx Philippe R., The natural killer activity of peritoneal fluid lymphocytes is decreased in women with endometriosis**Supported by the National Fund for Scientific Research, Brussels, Belgium., 10.1016/s0015-0282(16)55224-8
  23. Acién Pedro, Quereda Francisco, Campos Adolfo, Gomez-Torres Marı́a-José, Velasco Irene, Gutierrez Mercedes, Use of intraperitoneal interferon α-2b therapy after conservative surgery for endometriosis and postoperative medical treatment with depot gonadotropin-releasing hormone analog: a randomized clinical trial, 10.1016/s0015-0282(02)03330-7
  24. Acién Pedro, Quereda Francisco J., Gómez-Torres María-José, Bermejo Rosa, Gutierrez Mercedes, GnRH Analogues, Transvaginal Ultrasound-Guided Drainage and Intracystic Injection of Recombinant Interleukin-2 in the Treatment of Endometriosis, 10.1159/000070181
  25. Hornung D, J Clin Endocrinol Metab, 82, 1621 (1997)
  26. Koninckx Philippe R., Ussia Anastasia, Adamyan Leila, The role of the peritoneal cavity in adhesion formation, 10.1016/j.fertnstert.2012.04.017
  27. Arici Aydin, Oral Engin, Bukulmez Orhan, Buradagunta Sumati, Bahtiyar Ozan, Jones Ervin E., Monocyte chemotactic protein-1 expression in human preovulatory follicles and ovarian cells, 10.1016/s0165-0378(97)82476-x
  28. Dmowski W.P., Steele Russell W., Baker Glen F., Deficient cellular immunity in endometriosis, 10.1016/0002-9378(81)90598-6
  29. Hart David A., Curbing Inflammation in Multiple Sclerosis and Endometriosis: Should Mast Cells Be Targeted?, 10.1155/2015/452095
  30. Menzies F. M., Shepherd M. C., Nibbs R. J., Nelson S. M., The role of mast cells and their mediators in reproduction, pregnancy and labour, 10.1093/humupd/dmq053
  31. Kirchhoff Dennis, Kaulfuss Stefan, Fuhrmann Ulrike, Maurer Marcus, Zollner Thomas M, Mast cells in endometriosis: guilty or innocent bystanders?, 10.1517/14728222.2012.661415
  32. Kempuraj Duraisamy, Papadopoulou Nikoletta, Stanford Edward J., Christodoulou Spyridon, Madhappan Bhuvaneshwari, Sant Grannum R., Solage Kathleen, Adams Tayrickia, Theoharides Theoharis C., Increased Numbers of Activated Mast Cells in Endometriosis Lesions Positive for Corticotropin-Releasing Hormone and Urocortin, 10.1111/j.1600-0897.2004.00224.x
  33. Kyama Cleophas M, Debrock Sophie, Mwenda Jason M, D'Hooghe Thomas M, 10.1186/1477-7827-1-123
  34. Van Langendonckt A., Donnez J., Defrere S., Dunselman G. A.J., Groothuis P. G., Antiangiogenic and vascular-disrupting agents in endometriosis: pitfalls and promises, 10.1093/molehr/gan019
  35. de Ziegler Dominique, Borghese Bruno, Chapron Charles, Endometriosis and infertility: pathophysiology and management, 10.1016/s0140-6736(10)60490-4
  36. KYAMA C, OVERBERGH L, DEBROCK S, VALCKX D, VANDERPERRE S, MEULEMAN C, MIHALYI A, MWENDA J, MATHIEU C, DHOOGHE T, Increased peritoneal and endometrial gene expression of biologically relevant cytokines and growth factors during the menstrual phase in women with endometriosis, 10.1016/j.fertnstert.2005.11.060
  37. Kyama Cleophas M., Overbergh Lutgart, Mihalyi Attila, Meuleman Christel, Mwenda Jason M., Mathieu Chantal, D'Hooghe Thomas M., Endometrial and peritoneal expression of aromatase, cytokines, and adhesion factors in women with endometriosis, 10.1016/j.fertnstert.2007.02.057
  38. Gazvani R, Templeton A, Peritoneal environment, cytokines and angiogenesis in the pathophysiology of endometriosis, 10.1530/rep.0.1230217
  39. Harada Tasuku, Iwabe Tomio, Terakawa Naoki, Role of cytokines in endometriosis, 10.1016/s0015-0282(01)01816-7
  40. Sivridis E, Giatromanolaki A, Agnantis Niki, Anastasiadis P, Mast cell distribution and density in the normal uterus — metachromatic staining using lectins, 10.1016/s0301-2115(00)00564-9
  41. Zhang Jin, Nie Guiying, Jian Wang, Woolley David E., Salamonsen Lois A., Mast Cell Regulation of Human Endometrial Matrix Metalloproteinases: A Mechanism Underlying Menstruation1, 10.1095/biolreprod59.3.693
  42. Marbaix E., Kokorine I., Donnez J., Eeckhout Y., Courtoy P. J., Regulation and restricted expression of interstitial collagenase suggest a pivotal role in the initiation of menstruation, 10.1093/humrep/11.suppl_2.134
  43. Kokorine I, J Cell Sci, 109, 2151 (1996)
  44. Lin KQ, Zhejiang Da Xue Xue Bao Yi Xue Ban, 44, 269 (2015)
  45. Umezawa Masakazu, Sakata Chika, Tanaka Naomi, Tabata Masako, Takeda Ken, Ihara Tomomi, Sugamata Masao, Pathological study for the effects of in utero and postnatal exposure to diesel exhaust on a rat endometriosis model, 10.2131/jts.36.493
  46. Uchiide Ichiro, Ihara Tomomi, Sugamata Masao, Pathological evaluation of the rat endometriosis model, 10.1016/s0015-0282(02)03327-7
  47. ANAF V, CHAPRON C, ELNAKADI I, DEMOOR V, SIMONART T, NOEL J, Pain, mast cells, and nerves in peritoneal, ovarian, and deep infiltrating endometriosis, 10.1016/j.fertnstert.2006.03.057
  48. Sugamata Masao, Ihara Tomomi, Uchiide Ichiro, Increase of Activated Mast Cells in Human Endometriosis, 10.1111/j.1600-0897.2005.00254.x
  49. Paula Rubens, Oliani Antonio H., Vaz-Oliani Denise C. M., D’Ávila Solange C. G. P., Oliani Sonia M., Gil Cristiane D., The intricate role of mast cell proteases and the annexin A1-FPR1 system in abdominal wall endometriosis, 10.1007/s10735-014-9595-y
  50. MATSUZAKI SACHIKO, CANIS MICHEL, DARCHA CLAUDE, FUKAYA TAKAO, YAJIMA AKIRA, BRUHAT MAURICE A., Increased Mast Cell Density in Peritoneal Endometriosis Compared with Eutopic Endometrium with Endometriosis, 10.1111/j.1600-0897.1998.tb00420.x
  51. Zaitsu Masafumi, Narita Shin-Ichiro, Lambert K. Chad, Grady James J., Estes D. Mark, Curran Edward M., Brooks Edward G., Watson Cheryl S., Goldblum Randall M., Midoro-Horiuti Terumi, Estradiol activates mast cells via a non-genomic estrogen receptor-α and calcium influx, 10.1016/j.molimm.2006.09.030
  52. Bonds Rana S., Midoro-Horiuti Terumi, Estrogen effects in allergy and asthma : , 10.1097/aci.0b013e32835a6dd6
  53. Novella-Maestre Edurne, Herraiz Sonia, Vila-Vives José María, Carda Carmen, Ruiz-Sauri Amparo, Pellicer Antonio, Effect of antiangiogenic treatment on peritoneal endometriosis-associated nerve fibers, 10.1016/j.fertnstert.2012.07.1103
  54. KONNO Ryo, YAMADA-OKABE Hisafumi, FUJIWARA Hiroyuki, UCHIIDE Ichiro, SHIBAHARA Hiroaki, OHWADA Michitaka, IHARA Tomomi, SUGAMATA Masao, SUZUKI Mitsuaki, Role of immunoreactions and mast cells in pathogenesis of human endometriosis -morphologic study and gene expression analysis-, 10.1111/j.1749-0774.2003.tb00146.x
  55. OSUGA YUTAKA, KOGA KAORI, TSUTSUMI OSAMU, IGARASHI TOSHIO, OKAGAKI RYUGO, TAKAI YASUSHI, MATSUMI HIROTAKA, HIROI HISAHIKO, FUJIWARA TOSHIHIRO, MOMOEDA MIKIO, YANO TETSU, TAKETANI YUJI, TSUTSUMI OSAMU, Stem Cell Factor (SCF) Concentrations in Peritoneal Fluid of Women with or without Endometriosis, 10.1111/j.8755-8920.2000.440407.x
  56. Graziottin A, Urologia, 75, 67 (2008)
  57. Graziottin Alessandra, Gambini Dania, Bertolasi Laura, Genital and sexual pain in women, Neurology of Sexual and Bladder Disorders (2015) ISBN:9780444632470 p.395-412, 10.1016/b978-0-444-63247-0.00023-7
  58. Aich Anupam, Afrin Lawrence, Gupta Kalpna, Mast Cell-Mediated Mechanisms of Nociception, 10.3390/ijms161226151
  59. Zuo Yunxia, Perkins Nicholas M, Tracey David J, Geczy Carolyn L, Inflammation and hyperalgesia induced by nerve injury in the rat: a key role of mast cells : , 10.1016/s0304-3959(03)00261-6
  60. Ihara Tomomi, Uchiide Ichiro, Sugamata Masao, Light and electron microscopic evaluation of antileukotriene therapy for experimental rat endometriosis, 10.1016/j.fertnstert.2003.08.029
  61. Alvarez P., Bogen O., Chen X., Giudice L.C., Levine J.D., Ectopic endometrium-derived leptin produces estrogen-dependent chronic pain in a rat model of endometriosis, 10.1016/j.neuroscience.2013.11.008
  62. Iuvone Teresa, Affaitati Giannapia, De Filippis Daniele, Lopopolo Mariangela, Grassia Gianluca, Lapenna Domenico, Negro Luana, Costantini Raffaele, Vaia Massimo, Cipollone Francesco, Ialenti Armando, Giamberardino Maria Adele, Ultramicronized palmitoylethanolamide reduces viscerovisceral hyperalgesia in a rat model of endometriosis plus ureteral calculosis : role of mast cells, 10.1097/j.pain.0000000000000220
  63. Zhu LB, Zhejiang Da Xue Xue Bao Yi Xue Ban, 44, 278 (2015)
  64. Zhang Tao, Finn Deirdre Frances, Barlow James William, Walsh John Jarlath, Mast cell stabilisers, 10.1016/j.ejphar.2015.05.071
  65. Indraccolo Ugo, Barbieri Fabrizio, Effect of palmitoylethanolamide–polydatin combination on chronic pelvic pain associated with endometriosis: Preliminary observations, 10.1016/j.ejogrb.2010.01.008
  66. Engemise Samuel L., Willets Jonathon M., Emembolu Joseph O., Konje Justin C., The effect of the levonorgestrel-releasing intrauterine system, Mirena® on mast cell numbers in women with endometriosis undergoing symptomatic treatment, 10.1016/j.ejogrb.2011.09.007
  67. Alvarez Pedro, Levine Jon D., Screening the Role of Pronociceptive Molecules in a Rodent Model of Endometriosis Pain, 10.1016/j.jpain.2014.04.002
  68. Theron A. J., Steel H. C., Tintinger G. R., Gravett C. M., Anderson R., Feldman C., Cysteinyl Leukotriene Receptor-1 Antagonists as Modulators of Innate Immune Cell Function, 10.1155/2014/608930
  69. De Filippis D., Negro L., Vaia M., Cinelli M.P., Iuvone T., New Insights in Mast Cell Modulation by Palmitoylethanolamide, 10.2174/1871527311312010013
  70. Facci L., Dal Toso R., Romanello S., Buriani A., Skaper S. D., Leon A., Mast cells express a peripheral cannabinoid receptor with differential sensitivity to anandamide and palmitoylethanolamide., 10.1073/pnas.92.8.3376
  71. Cobellis Luigi, Castaldi Maria Antonietta, Giordano Valentino, Trabucco Elisabetta, De Franciscis Pasquale, Torella Marco, Colacurci Nicola, Effectiveness of the association micronized N-Palmitoylethanolamine (PEA)–transpolydatin in the treatment of chronic pelvic pain related to endometriosis after laparoscopic assessment: a pilot study, 10.1016/j.ejogrb.2011.04.011
  72. Lo Monte MG, Minerva Ginecol, 65, 453 (2013)
  73. Keppel Hesselink Jan M., Effectiveness of the association micronized N-palmitoylethanolamine (PEA)-transpolydatin in the treatment of chronic pelvic pain, 10.1016/j.ejogrb.2011.06.005
  74. Lockhat F.B., The evaluation of the effectiveness of an intrauterine-administered progestogen (levonorgestrel) in the symptomatic treatment of endometriosis and in the staging of the disease, 10.1093/humrep/deh004
  75. Vasiadi M., Kempuraj D., Boucher W., Kalogeromitros D., Theoharides T.C., Progesterone Inhibits Mast Cell Secretion, 10.1177/039463200601900408
  76. Korzus Edward, Nagase Hideaki, Rydell Russell, Travis James, The Mitogen-activated Protein Kinase and JAK-STAT Signaling Pathways Are Required for an Oncostatin M-responsive Element-mediated Activation of Matrix Metalloproteinase 1 Gene Expression, 10.1074/jbc.272.2.1188
  77. Rawlings J. S., The JAK/STAT signaling pathway, 10.1242/jcs.00963
  78. Howell J.B.L., Altounyan R.E.C., A DOUBLE-BLIND TRIAL OF DISODIUM CROMOGLYCATE IN THE TREATMENT OF ALLERGIC BRONCHIAL ASTHMA, 10.1016/s0140-6736(67)90499-0
  79. Kahlich R, J Hyg Epidemiol Microbiol Immunol, 23, 11 (1979)
  80. Mašek K., Perlík F., Klíma J., Kahlich R., Prophylactic efficacy of N-2-hydroxyethyl palmitamide (Impulsin®) in acute respiratory tract infections, 10.1007/bf00560353
  81. Colette S., Donnez J., Modèles animaux dans la recherche expérimentale sur l’endométriose, 10.1016/j.gyobfe.2012.07.009
  82. Dehoux Jean-Paul, Defrère Sylvie, Squifflet Jean, Donnez Olivier, Polet Roland, Mestdagt Mélanie, Foidart Jean-Michel, Van Langendonckt Anne, Donnez Jacques, Is the baboon model appropriate for endometriosis studies?, 10.1016/j.fertnstert.2011.06.037
  83. Defrère Sylvie, Van Langendonckt Anne, Ramos Reinaldo González, Jouret Mathieu, Mettlen Marcel, Donnez Jacques, Quantification of endometriotic lesions in a murine model by fluorimetric and morphometric analyses, 10.1093/humrep/dei387
  84. Peterse Daniëlle P., Fassbender Amelie, O Dorien F., Vanhie Arne, Saunders Philippa, Vriens Joris, Binda M. Mercedes, D’Hooghe Thomas M., Laparoscopic Surgery : A New Technique to Induce Endometriosis in a Mouse Model, 10.1177/1933719116638178
  85. Donnez Olivier, Van Langendonckt Anne, Defrère Sylvie, Colette Sébastien, Van Kerk Olivier, Dehoux Jean-Paul, Squifflet Jean, Donnez Jacques, Induction of endometriotic nodules in an experimental baboon model mimicking human deep nodular lesions, 10.1016/j.fertnstert.2012.10.032
  86. Donnez Olivier, Soares Michelle, Defrère Sylvie, Dehoux Jean-Paul, van Langendonckt Anne, Donnez Jacques, Dolmans Marie-Madeleine, Colette Sébastien, Nerve fiber density in deep nodular endometriotic lesions induced in a baboon experimental model, 10.1016/j.fertnstert.2013.06.014
  87. Donnez Olivier, Orellana Renan, Van Kerk Olivier, Dehoux Jean-Paul, Donnez Jacques, Dolmans Marie-Madeleine, Invasion process of induced deep nodular endometriosis in an experimental baboon model: similarities with collective cell migration?, 10.1016/j.fertnstert.2015.05.011
  88. Katz Howard R., Austen K. Frank, Mast Cell Deficiency, A Game of Kit and Mouse, 10.1016/j.immuni.2011.11.004
  89. Chatterjea Devavani, Wetzel Abigail, Mack Madison, Engblom Camilla, Allen Juliann, Mora-Solano Carolina, Paredes Luisa, Balsells Evelyn, Martinov Tijana, Mast cell degranulation mediates compound 48/80-induced hyperalgesia in mice, 10.1016/j.bbrc.2012.07.074
  90. Finn D F, Walsh J J, Twenty-first century mast cell stabilizers : Twenty-first century mast cell stabilizers, 10.1111/bph.12138
  91. Malaviya Ravi, Zhu DeMin, Dibirdik Ilker, Uckun Fatih M., Targeting Janus Kinase 3 in Mast Cells Prevents Immediate Hypersensitivity Reactions and Anaphylaxis, 10.1074/jbc.274.38.27028
  92. Sudbeck Elise A., Jennissen Jason D., Liu Xing-Ping, Uckun Fatih M., An inhibitor of Janus kinase 3: 4-(4-hydroxyphenylamino)-6,7-dimethoxyquinazolin-1-ium chloride methanol solvate, 10.1107/s0108270100007496
  93. Uckun Fatih M., Tibbles Heather, Ozer Zahide, Qazi Sanjive, Vassilev Alexei, Anti-inflammatory activity profile of JANEX-1 in preclinical animal models, 10.1016/j.bmc.2007.10.066
  94. Santulli Pietro, Marcellin Louis, Tosti Claudia, Chouzenoux Sandrine, Cerles Olivier, Borghese Bruno, Batteux Frédéric, Chapron Charles, MAP kinases and the inflammatory signaling cascade as targets for the treatment of endometriosis?, 10.1517/14728222.2015.1090974
  95. Li Liangchang, Jin Guangyu, Jiang Jingzhi, Zheng Mingyu, Jin Yan, Lin Zhenhua, Li Guangzhao, Choi Yunho, Yan Guanghai, Cornuside inhibits mast cell-mediated allergic response by down-regulating MAPK and NF-κB signaling pathways, 10.1016/j.bbrc.2016.03.007
  96. Zhang Ning, Li Hong, Jia Jihui, He Mingqiang, Anti-inflammatory effect of curcumin on mast cell-mediated allergic responses in ovalbumin-induced allergic rhinitis mouse, 10.1016/j.cellimm.2015.09.010