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Silymarin antiproliferative and apoptotic effects: Insights into its clinical impact in various types of cancer

Tahereh HosseinabadiDepartment of Pharmacognosy and Biotechnology, School of Pharmacy Shahid Beheshti University of Medical Sciences Tehran IranZahra LorigooiniMedical Plants Research Center, Basic Health Sciences Institute Shahrekord University of Medical Sciences Shahrekord IranMaryam TabarzadProtein Technology Research Center Shahid Beheshti University of Medical Sciences Tehran IranBahare SalehiStudent Research Committee, School of Medicine Bam University of Medical Sciences Bam IranCélia F. RodriguesLEPABE–Department of Chemical Engineering, Faculty of Engineering University of Porto Porto PortugalNatália MartinsInstitute for Research and Innovation in Health (i3S) University of Porto Porto PortugalJavad Sharifi‐RadZabol Medicinal Plants Research Center Zabol University of Medical Sciences Zabol Iran
2019en
ABI

Annotatsiya

Silymarin is a complex extract isolated from the plant Silybum marianum, widely known for its prominent antioxidant and hepatoprotective effects, although increasing evidences have reported extraordinary antiproliferative and apoptotic abilities. As a result, several signaling pathways involved in cell cycle control, cell proliferation, and cell death have been deconvoluted as critical mechanisms. In this regard, cyclin and cyclin-dependent pathways have been the most studied ones. Following that, apoptotic pathways, such as p53, Akt, STAT-3, Ras, and caspases pathways, have been extensively studied, although other mechanisms involved in inflammation and angiogenesis have also been highlighted as silymarin-likely targets in cancer therapy. Therefore, the main challenge of this review is to discuss the diverse molecular mechanisms for silymarin antiproliferative and apoptotic effects; most of them largely studied in various types of cancers so far. Clinical trials and combination therapies related to silymarin application in cancer prevention and treatment are presented as well.

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