Pharmaceuticals targeting signaling pathways of endometriosis as potential new medical treatment: A review.
Sze Wan HungRuizhe ZhangZhouyurong TanJacqueline Pui Wah ChungTao ZhangChi Chiu WangPublished in: Medicinal research reviews (2021)
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-κB, Rho/ROCK, reactive oxidative stress, tumor necrosis factor, transforming growth factor-β, Wnt/β-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.
Keyphrases
- anti inflammatory
- signaling pathway
- induced apoptosis
- pi k akt
- vascular endothelial growth factor
- cell cycle arrest
- oxidative stress
- epithelial mesenchymal transition
- transforming growth factor
- endothelial cells
- healthcare
- cell proliferation
- endoplasmic reticulum stress
- clinical trial
- dna damage
- cancer therapy
- systematic review
- gene expression
- diabetic rats
- ischemia reperfusion injury
- rheumatoid arthritis
- stem cells
- human health
- polycystic ovary syndrome
- heat shock
- cell migration
- skeletal muscle
- immune response
- phase ii
- drug induced
- combination therapy
- endometrial cancer
- fluorescent probe
- lps induced
- adipose tissue
- insulin resistance