Targeting of oncogenic signaling pathways by berberine for treatment of colorectal cancer

被引:0
|
作者
Jamal Hallajzadeh
Parisa Maleki Dana
Moein Mobini
Zatollah Asemi
Mohammad Ali Mansournia
Mehran Sharifi
Bahman Yousefi
机构
[1] Maragheh University of Medical Sciences,Department of Biochemistry and Nutrition, Research Center for Evidence
[2] Kashan University of Medical Sciences,Based Health Management
[3] University of Calgary,Research Center for Biochemistry and Nutrition in Metabolic Diseases
[4] Tehran University of Medical Sciences,Faculty of Kinesiology
[5] Isfahan University of Medical Sciences,Department of Epidemiology and Biostatistics, School of Public Health
[6] Tabriz University of Medical Sciences,Department of Hematology and Oncology, School of Medicine
来源
Medical Oncology | 2020年 / 37卷
关键词
Berberine; Apoptosis; microRNA; Signaling pathway; Inflammation; Oxidative stress;
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摘要
Studies indicate that inhibiting a single signaling pathway or one single product of a gene is insufficient for the prevention and treatment of cancer. This is due to the fact that dysregulation must occur in more than 500 genes in order to produce a cancerous phenotype. Despite this evidence, available drugs used for cancer treatment focus on a single target. Meanwhile, berberine as a nutraceutical is capable of targeting various processes involved in tumor development including proliferation, invasion, angiogenesis, and metastasis. In comparison with synthetic agents, berberine is cheaper, safer, and more available. Berberine has shown anti-inflammatory properties which make it an ideal option in order to prevent inflammation-associated cancers. Colorectal cancer is one of the most common cancers all over the world and its incidence is increasing each day. Therefore, further investigations about berberine could be helpful in the discovery of novel agents for preventing and/or treating colorectal cancer. This review emphasizes the studies investigating the roles of berberine in colorectal cancer such as controlling cell signaling pathways, inducing apoptosis, regulating microRNAs, attenuating oxidative stress, and affecting inflammation.
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