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Pharmaceuticals targeting signaling pathways of endometriosis as potential new medical treatment: A review

期刊

MEDICINAL RESEARCH REVIEWS
卷 41, 期 4, 页码 2489-2564

出版社

WILEY
DOI: 10.1002/med.21802

关键词

endometriosis; pathophysiology; pathways; pharmaceuticals; targets; treatments

资金

  1. General Research Fund from Research Grants Council, Hong Kong [475012]
  2. Health and Medical Research Fund from Food and Health Bureau, Hong Kong [03141386]
  3. Innovation and Technology Fund from Innovation and Technology Commission, Hong Kong [ITS/209/12]
  4. UGC Direct Grant from The Chinese University of Hong Kong, Hong Kong
  5. HKOG Trust Fund, Hong Kong
  6. National Natural Science Foundation of China, China [81974225]

向作者/读者索取更多资源

Endometriosis is a condition where endometrial tissues are found outside the uterus. The pathophysiological mechanisms involve various signaling pathways, including proliferation, apoptosis, migration, invasion, fibrosis, angiogenesis, oxidative stress, inflammation, and immune escape. Current treatments mainly focus on hormonal and symptomatic relief, prompting the need for new pharmaceuticals targeting specific molecular pathways.
Endometriosis (EM) is defined as endometrial tissues found outside the uterus. Growth and development of endometriotic cells in ectopic sites can be promoted via multiple pathways, including MAPK/MEK/ERK, PI3K/Akt/mTOR, NF-kappa B, Rho/ROCK, reactive oxidative stress, tumor necrosis factor, transforming growth factor-beta, Wnt/beta-catenin, vascular endothelial growth factor, estrogen, and cytokines. The underlying pathophysiological mechanisms include proliferation, apoptosis, autophagy, migration, invasion, fibrosis, angiogenesis, oxidative stress, inflammation, and immune escape. Current medical treatments for EM are mainly hormonal and symptomatic, and thus the development of new, effective, and safe pharmaceuticals targeting specific molecular and signaling pathways is needed. Here, we systematically reviewed the literature focused on pharmaceuticals that specifically target the molecular and signaling pathways involved in the pathophysiology of EM. Potential drug targets, their upstream and downstream molecules with key aberrant signaling, and the regulatory mechanisms promoting the growth and development of endometriotic cells and tissues were discussed. Hormonal pharmaceuticals, including melatonin, exerts proapoptotic via regulating matrix metallopeptidase activity while nonhormonal pharmaceutical sorafenib exerts antiproliferative effect via MAPK/ERK pathway and antiangiogenesis activity via VEGF/VEGFR pathway. N-acetyl cysteine, curcumin, and ginsenoside exert antioxidant and anti-inflammatory effects via radical scavenging activity. Natural products have high efficacy with minimal side effects; for example, resveratrol and epigallocatechin gallate have multiple targets and provide synergistic efficacy to resolve the complexity of the pathophysiology of EM, showing promising efficacy in treating EM. Although new medical treatments are currently being developed, more detailed pharmacological studies and large sample size clinical trials are needed to confirm the efficacy and safety of these treatments in the near future.

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