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
[11]   Medicinal plants and cancer chemoprevention [J].
Desai, Avni G. ;
Qazi, Ghulam N. ;
Ganju, Ramesh K. ;
El-Tamer, Mahmoud ;
Singh, Jaswant ;
Saxena, Ajit K. ;
Bedi, Yashbir S. ;
Taneja, Subhash C. ;
Bhat, Hari K. .
CURRENT DRUG METABOLISM, 2008, 9 (07) :581-591
[12]  
Dörrie J, 2001, CANCER RES, V61, P4731
[13]   Apoptosis: A review of programmed cell death [J].
Elmore, Susan .
TOXICOLOGIC PATHOLOGY, 2007, 35 (04) :495-516
[14]   Resveratrol attenuates the anticancer efficacy of paclitaxel in human breast cancer cells in vitro and in vivo [J].
Fukui, Masayuki ;
Yamabe, Noriko ;
Zhu, Bao Ting .
EUROPEAN JOURNAL OF CANCER, 2010, 46 (10) :1882-1891
[15]  
Geng Wf, 2012, J CWNU NATURAL SCI, P03
[16]   Resveratrol suppresses prostate cancer progression in transgenic mice [J].
Harper, Curt E. ;
Patel, Brijesh B. ;
Wang, Jun ;
Arabshahi, Alireza ;
Eltoum, Isam A. ;
Lamartiniere, Coral A. .
CARCINOGENESIS, 2007, 28 (09) :1946-1953
[17]   Regulated necrosis-related molecule mRNA expression in humans and mice and in murine acute tissue injury and systemic autoimmunity leading to progressive organ damage, and progressive fibrosis [J].
Honarpisheh, Mohsen ;
Desai, Jyaysi ;
Maschner, Julian A. ;
Weidenbusch, Marc ;
Lech, Maciej ;
Vielhauer, Volker ;
Anders, Hans-Joachim ;
Mulay, Shrikant R. .
BIOSCIENCE REPORTS, 2016, 36
[18]   Resveratrol enhances anticancer effects of paclitaxel in HepG2 human liver cancer cells [J].
Jiang, Qin ;
Yang, Manyi ;
Qu, Zhan ;
Zhou, Jixiang ;
Zhang, Qi .
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2017, 17
[19]   Effects of resveratrol on cerebral blood flow variables and cognitive performance in humans: a double-blind, placebo-controlled, crossover investigation [J].
Kennedy, David O. ;
Wightman, Emma L. ;
Reay, Jonathon L. ;
Lietz, Georg ;
Okello, Edward J. ;
Wilde, Anthea ;
Haskell, Crystal F. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2010, 91 (06) :1590-1597
[20]   Death receptor signals to mitochondria [J].
Khosravi-Far, R ;
Esposti, MD .
CANCER BIOLOGY & THERAPY, 2004, 3 (11) :1051-1057