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

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机构: [1]Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong. [2]Center for Reproductive Medicine, Henan Key Laboratory of Reproduction and Genetics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou. [3]Reproduction and Development, Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong. [4]School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong. [5]Chinese University of Hong Kong-Sichuan University Joint Laboratory in Reproductive Medicine, The Chinese University of Hong Kong, Hong Kong.
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关键词: endometriosis pathophysiology pathways pharmaceuticals targets treatments

摘要:
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. © 2021 The Authors. Medicinal Research Reviews published by Wiley Periodicals LLC.

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出版当年[2021]版
大类 | 1 区 医学
小类 | 1 区 药物化学 1 区 药学
最新[2023]版
大类 | 1 区 医学
小类 | 1 区 药物化学 1 区 药学
第一作者:
第一作者机构: [1]Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong.
通讯作者:
通讯机构: [1]Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong. [3]Reproduction and Development, Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong. [4]School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong. [5]Chinese University of Hong Kong-Sichuan University Joint Laboratory in Reproductive Medicine, The Chinese University of Hong Kong, Hong Kong. [*1]Department of Obstetrics & Gynaecology,The Chinese University of Hong Kong, 1/F,Special Block EF, Prince of Wales Hospital,Shatin, N.T., Hong Kong.
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