Role of inflammation in benign gynecologic disorders: from pathogenesis to novel therapies

被引:62
作者
AlAshqar, Abdelrahman [1 ,2 ]
Reschke, Lauren [1 ]
Kirschen, Gregory W. [1 ]
Borahay, Mostafa A. [1 ]
机构
[1] Johns Hopkins Univ, Dept Gynecol & Obstet, 4940 Eastern Ave, Baltimore, MD 21224 USA
[2] Kuwait Univ, Dept Obstet & Gynecol, Kuwait, Kuwait
基金
美国国家卫生研究院;
关键词
adenomyosis; chemokine; cytokine; endometriosis; growth factor; infertility; inflammation; prostaglandin; uterine leiomyoma; TUMOR-NECROSIS-FACTOR; MIGRATION INHIBITORY FACTOR; FACTOR-KAPPA-B; ENDOMETRIAL STROMAL CELLS; CHEMOTACTIC PROTEIN-1 EXPRESSION; ENDOTHELIAL GROWTH-FACTOR; NATURAL-KILLER-CELLS; INDUCED INTERLEUKIN-8 PRODUCTION; PERITONEAL-FLUID MACROPHAGES; RECURRENT PREGNANCY LOSS;
D O I
10.1093/biolre/ioab054
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Emerging evidence supports the notion that inflammation fosters the development of common benign gynecologic disorders, including uterine leiomyoma, endometriosis, and adenomyosis. Numerous cytokines, chemokines, and growth and transcription factors have indisputable roles in the establishment and maintenance of benign gynecologic disorders by initiating complex cascades that promote proliferation, angiogenesis, and lesion progression. The interaction between inflammation and benign gynecologic disorders is orchestrated by a plethora of factors, including sex steroids, genetics, epigenetics, extracellular matrix, stem cells, cardiometabolic risk factors, diet, vitamin D, and the immune system. The role of inflammation in these disorders is not limited to local pathobiology but also extends to involve clinical sequelae that range from those confined to the reproductive tract, such as infertility and gynecologic malignancies, to systemic complications such as cardiovascular disease. Enhanced understanding of the intricate mechanisms of this association will introduce us to unvisited pathophysiological perspectives and guide future diagnostic and therapeutic implications aimed at reducing the burden of these disorders. Utilization of inflammatory markers, microRNA, and molecular imaging as diagnostic adjuncts may be valuable, noninvasive techniques for prompt detection of benign gynecologic disorders. Further, use of novel as well as previously established therapeutics, such as immunomodulators, hormonal treatments, cardiometabolic medications, and cyclooxygenase-2 and NF-kappa B inhibitors, can target inflammatory pathways involved in their pathogenesis. In this comprehensive review, we aim to dissect the existing literature on the role of inflammation in benign gynecologic disorders, including the proposed underlying mechanisms and complex interactions, its contribution to clinical sequelae, and the clinical implications this role entails. Summary sentence Reconceptualizing common benign gynecologic disorders as having inherent inflammatory pathobiology will introduce us to previously unvisited perspectives of their development and devise novel clinical implications aimed at reducing their burden.
引用
收藏
页码:7 / 31
页数:25
相关论文
共 279 条
[1]   Treatment of endometriosis with transvaginal ultrasound-guided drainage under GnRH analogues and recombinant interleukin-2 left in the cysts [J].
Acién, P ;
Pérez-Albert, G ;
Quereda, FJ ;
Sánchez-Ferrer, M ;
García- Almela, A ;
Velasco, I .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 2005, 60 (04) :224-231
[2]   Simvastatin ameliorates altered mechanotransduction in uterine leiomyoma cells [J].
Afrin, Sadia ;
Islam, Md Soriful ;
Patzkowsky, Kristin ;
Malik, Minnie ;
Catherino, William H. ;
Segars, James H. ;
Borahay, Mostafa A. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2020, 223 (05) :733.e1-733.e14
[3]   Effects of rapamycin on the epithelial-to-mesenchymal transition of human peritoneal mesothelial cells [J].
Aguilera, A ;
Aroeira, LS ;
Ramírez-Huesca, M ;
Pérez-Lozano, ML ;
Cirugeda, A ;
Bajo, MA ;
Del Paso, G ;
Valenzuela-Fernández, A ;
Sánchez-Tomero, JA ;
López-Cabrera, M ;
Selgas, R .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 2005, 28 (02) :164-169
[4]   Immune-inflammation gene signatures in endometriosis patients [J].
Ahn, Soo Hyun ;
Khalaj, Kasra ;
Young, Steven L. ;
Lessey, Bruce A. ;
Koti, Madhuri ;
Tayade, Chandrakant .
FERTILITY AND STERILITY, 2016, 106 (06) :1420-+
[5]   Pathophysiology and Immune Dysfunction in Endometriosis [J].
Ahn, Soo Hyun ;
Monsanto, Stephany P. ;
Miller, Caragh ;
Singh, Sukhbir S. ;
Thomas, Richard ;
Tayade, Chandrakant .
BIOMED RESEARCH INTERNATIONAL, 2015, 2015
[6]   Ectopic endometrial cells express high concentrations of interleukin (IL)-8 in vivo regardless of the menstrual cycle phase and respond to oestradiol by up-regulating IL-1-induced IL-8 expression in vitro [J].
Akoum, A ;
Lawson, C ;
McColl, S ;
Villeneuve, M .
MOLECULAR HUMAN REPRODUCTION, 2001, 7 (09) :859-866
[7]   Silencing Med12 Gene Reduces Proliferation of Human Leiomyoma Cells Mediated via Wnt/β-Catenin Signaling Pathway [J].
Al-Hendy, Ayman ;
Laknaur, Archana ;
Diamond, Michael P. ;
Ismail, Nahed ;
Boyer, Thomas G. ;
Halder, Sunil K. .
ENDOCRINOLOGY, 2017, 158 (03) :592-603
[8]   The Detection of Uterine Leiomyoma (Fibroid) Calcifications on 18F-NaF PET/CT [J].
Al-Zaghal, Abdullah ;
Werner, Thomas J. ;
Hoilund-Carlsen, Poul F. ;
Alavi, Abass .
CLINICAL NUCLEAR MEDICINE, 2018, 43 (08) :E287-E288
[9]   Cardiometabolic Risk Factors and Benign Gynecologic Disorders [J].
AlAshqar, Abdelrahman ;
Patzkowsky, Kristin ;
Afrin, Sadia ;
Wild, Robert ;
Taylor, Hugh S. ;
Borahay, Mostafa A. .
OBSTETRICAL & GYNECOLOGICAL SURVEY, 2019, 74 (11) :661-673
[10]   The Systemic Effects of Endometriosis [J].
Alderman, Myles H., III ;
Yoder, Nicole ;
Taylor, Hugh S. .
SEMINARS IN REPRODUCTIVE MEDICINE, 2017, 35 (03) :263-270