Efficacy of resveratrol against breast cancer and hepatocellular carcinoma cell lines

被引:12
作者
ALkharashi, Nouf A. [1 ]
机构
[1] Prince Sattam bin Abdulaziz Univ, Coll Educ, Dept Home Eon, Al Kharj, Saudi Arabia
关键词
MTT; resveratrol; proliferation; MCF-7; HepG2 cell line; APOPTOSIS; CASPASE-9; GROWTH; DEATH;
D O I
10.15537/smj.2023.44.3.20220768
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To evaluate the anti-cancer effect of resveratrol on Michigan cancer foundation-7 (MCF-7) and hepatoblastoma cell line (HepG2) cells.Methods: The study was carried out at the Department of Botany and Microbiology, Prince Sattam bin Abdulaziz University, Al-kharj, Saudi Arabia, from August 2022 to October 2022. Different concentrations of resveratrol were added to the MCF-7 and HepG2 cell lines. Cell death and proliferation were measured with MTT and Trypan blue exclusion assays. Apoptosis markers were assessed by using a quantitative PCR assay (qPCR).Results: The resveratrol was shown to suppress the proliferation of MCF-7 and HepG2 cells at dose-and time-dependent. The cytotoxic effect of resveratrol was observed even at 100 & mu;M after 24 hours. In comparison to untreated cells, resveratrol treatment reduced the viability of MCF-7 cells to roughly 57.5% with a half maximal inhibitory concentration (IC50) of 51.18 & mu;M and HepG2 cells to 56.2% with an IC50 of 57.4 & mu;M. Furthermore, in the tested cell lines, resveratrol was able to induce apoptosis mediated by elevated apoptosis markers.Conclusion: Resveratrol appears to be an excellent candidate agent in anticancer therapy in various human cancers.
引用
收藏
页码:246 / 252
页数:7
相关论文
共 50 条
[1]  
Aggarwal BB, 2004, ANTICANCER RES, V24, P2783
[2]   Endogenous IGFBP-3 Mediates Intrinsic Apoptosis Through Modulation of Nur77 Phosphorylation and Nuclear Export [J].
Agostini-Dreyer, Allyson ;
Jetzt, Amanda E. ;
Stires, Hillary ;
Cohick, Wendie S. .
ENDOCRINOLOGY, 2015, 156 (11) :4141-4151
[3]   Resveratrol enhances the cytotoxic profile of docetaxel and doxorubicin in solid tumour cell lines in vitro [J].
Al-Abd, A. M. ;
Mahmoud, A. M. ;
El-Sherbiny, G. A. ;
El-Moselhy, M. A. ;
Nofal, S. M. ;
El-Latif, H. A. ;
El-Eraky, W. I. ;
El-Shemy, H. A. .
CELL PROLIFERATION, 2011, 44 (06) :591-601
[4]  
Alotaibi Moureq R, 2018, Asian Pac J Cancer Prev, V19, P777
[5]  
Amjad M.T., 2022, Cancer Chemotherapy
[6]  
Banerjee S, 2002, CANCER RES, V62, P4945
[7]   Therapeutic potential of resveratrol:: the in vivo evidence [J].
Baur, Joseph A. ;
Sinclair, David A. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (06) :493-506
[8]   Biological effects of resveratrol [J].
Bhat, KPL ;
Kosmeder, JW ;
Pezzuto, JM .
ANTIOXIDANTS & REDOX SIGNALING, 2001, 3 (06) :1041-1064
[9]   Anticancer Molecular Mechanism of Protocatechuic Acid Loaded on Folate Coated Functionalized Graphene Oxide Nanocomposite Delivery System in Human Hepatocellular Carcinoma [J].
Buskaran, Kalaivani ;
Bullo, Saifullah ;
Hussein, Mohd Zobir ;
Masarudin, Mas Jaffri ;
Mohd Moklas, Mohamad Aris ;
Fakurazi, Sharida .
MATERIALS, 2021, 14 (04) :1-26
[10]   RIP1-dependent Bid cleavage mediates TNFα-induced but Caspase-3-independent cell death in L929 fibroblastoma cells [J].
Chen G. ;
Cheng X. ;
Zhao M. ;
Lin S. ;
Lu J. ;
Kang J. ;
Yu X. .
Apoptosis, 2015, 20 (1) :92-109