Protective Effect of Resveratrol against Glioblastoma: A Review

被引:6
|
作者
Ashrafizadeh, Milad [1 ]
Mohammadinejad, Reza [2 ]
Farkhondeh, Tahereh [3 ,4 ]
Samarghandian, Saeed [5 ]
机构
[1] Sabanci Univ, Fac Engn & Nat Sci, Univ Caddesi 27, TR-34956 Istanbul, Turkey
[2] Sabanci Univ, Nanotechnol Res & Applicat Ctr SUNUM, TR-34956 Istanbul, Turkey
[3] Birjand Univ Med Sci BUMS, Med Toxicol & Drug Abuse Res Ctr MTDRC, Birjand, Iran
[4] Birjand Univ Med Sci, Fac Pharm, Birjand, Iran
[5] Neyshabur Univ Med Sci, Noncommunicable Dis Res Ctr, Neyshabur, Iran
关键词
Resveratrol; glioblastoma; brain tumor; cancer therapy; medicinal herbs; central nervous system; EPITHELIAL-MESENCHYMAL TRANSITION; MESSENGER-RNA EXPRESSION; DNA TOPOISOMERASE-II; BLOOD-BRAIN-BARRIER; GLIOMA STEM-CELLS; NF-KAPPA-B; PARKINSONS-DISEASE; APOLIPOPROTEIN-E; MATRIX METALLOPROTEINASES; DOWN-REGULATION;
D O I
10.2174/1871520620666200929151139
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: One of the most common tumors of the central nervous system is glioblastoma (GBM). Objective: There is not still an appropriate cure for this malignant tumor. Plant-derived natural products have demonstrated great potential in cancer therapy, and resveratrol (Res) is among them. Therefore, the current study focused on the protective effect of resveratrol against glioblastoma and its underlying mechanism. Methods: PubMed, Medline, Scopus, Web of Science, and Google Scholar were searched by using the following keywords: Resveratrol, Glioblastoma, Brain tumor, Cancer therapy, Medicinal herbs to July 2020. Results: Res is a non-flavonoid polyphenol responsible for the protection of plants against pathogen attacks. Res has multiple pharmacological effects, including antioxidant, anti-inflammatory, anti-diabetic, and anti-tumor. Res is capable of penetration into the blood-brain barrier, making it suitable for brain tumor therapy. Besides, Res targets various molecular signaling pathways in cancer therapy. Conclusion: In the present review, it was found that Res administration is beneficial in GBM therapy by inhibition of proliferation, viability, and migration via modulation of molecular pathways.
引用
收藏
页码:1216 / 1227
页数:12
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