CLC number: R737.9
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2017-01-04
Cited: 1
Clicked: 6353
Shu-min Liu, Shi-yi Ou, Hui-hua Huang. Green tea polyphenols induce cell death in breast cancer MCF-7 cells through induction of cell cycle arrest and mitochondrial-mediated apoptosis[J]. Journal of Zhejiang University Science B, 2017, 18(2): 89-98.
@article{title="Green tea polyphenols induce cell death in breast cancer MCF-7 cells through induction of cell cycle arrest and mitochondrial-mediated apoptosis",
author="Shu-min Liu, Shi-yi Ou, Hui-hua Huang",
journal="Journal of Zhejiang University Science B",
volume="18",
number="2",
pages="89-98",
year="2017",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1600022"
}
%0 Journal Article
%T Green tea polyphenols induce cell death in breast cancer MCF-7 cells through induction of cell cycle arrest and mitochondrial-mediated apoptosis
%A Shu-min Liu
%A Shi-yi Ou
%A Hui-hua Huang
%J Journal of Zhejiang University SCIENCE B
%V 18
%N 2
%P 89-98
%@ 1673-1581
%D 2017
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1600022
TY - JOUR
T1 - Green tea polyphenols induce cell death in breast cancer MCF-7 cells through induction of cell cycle arrest and mitochondrial-mediated apoptosis
A1 - Shu-min Liu
A1 - Shi-yi Ou
A1 - Hui-hua Huang
J0 - Journal of Zhejiang University Science B
VL - 18
IS - 2
SP - 89
EP - 98
%@ 1673-1581
Y1 - 2017
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1600022
Abstract: In order to study the molecular mechanisms of green tea polyphenols (GTPs) in treatment or prevention of breast cancer, the cytotoxic effects of GTPs on five human cell lines (MCF-7, A549, Hela, PC3, and HepG2 cells) were determined and the antitumor mechanisms of GTPs in MCF-7 cells were analyzed. The results showed that GTPs exhibited a broad spectrum of inhibition against the detected cancer cell lines, particularly the MCF-7 cells. Studies on the mechanisms revealed that the main modes of cell death induced by GTPs were cell cycle arrest and mitochondrial-mediated apoptosis. Flow cytometric analysis showed that GTPs mediated cell cycle arrest at both G1/M and G2/M transitions. GTP dose dependently led to apoptosis of MCF-7 cells via the mitochondrial pathways, as evidenced by induction of chromatin condensation, reduction of mitochondrial membrane potential (ΔΨm), improvement in the generation of reactive oxygen species (ROS), induction of DNA fragmentation, and activations of caspase-3 and caspase-9 in the present paper.
[1]Baregamian, N., Song, J., Bailey, C.E., et al., 2009. Tumor necrosis factor-α and apoptosis signal-regulating kinase 1 control reactive oxygen species release, mitochondrial autophagy and c-Jun N-terminal kinase/p38 phosphorylation during necrotizing enterocolitis. Oxid. Med. Cell. Longev., 2(5):297-306.
[2]Boyle, P., Levin, B., 2008. World Cancer Report 2008. International Agency for Research on Cancer, Lyon, France.
[3]British Standards Institution, 2005. BS ISO 14502-1:2005. Determination of substances characteristic of green and black tea. Content of total polyphenols in tea. Colorimetric method using Folin-Ciocalteu reagent. British Standards Institution, London, UK, p.1-6. http://shop.bsigroup.com/ProductDetail/?pid=000000000030153463
[4]Chakraborty, D., Bishayee, K., Ghosh, S., et al., 2012. [6]-Gingerol induces caspase 3 dependent apoptosis and autophagy in cancer cells: drug-DNA interaction and expression of certain signal genes in HeLa cells. Eur. J. Pharmacol., 694(1-3):20-29.
[5]Cotran, R.S., Kumar, V., Collins, T., et al., 1999. Robbins Pathologic Basis of Disease, 6th Ed. WB Saunders, Philadelphia.
[6]Crews, C.M., Mohan, R., 2000. Small-molecule inhibitors of the cell cycle. Curr. Opin. Chem. Biol., 4(1):47-53.
[7]Ferlay, J., Shin, H., Bray, F., et al., 2010. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int. J. Cancer, 127(12):2893-2917.
[8]González, S.E.F., Anguiano, E.A., Herrera, A.M., et al., 2013. Cytotoxic, pro-apoptotic, pro-oxidant, and non-genotoxic activities of a novel copper(II) complex against human cervical cancer. Toxicology, 314(1):155-165.
[9]Hail, N.Jr., Carter, B.Z., Konopleva, M., 2006. Apoptosis effector mechanisms: a requiem performed in different keys. Apoptosis, 11(6):889-904.
[10]Hail, N.Jr., Cortes, M., Drake, E.N., et al., 2008. Cancer chemoprevention: a radical perspective. Free Radical Biol. Med., 45(2):97-110.
[11]Herold, M.J., Kuss, A.W., Kraus, C., et al., 2002. Mitochondria-dependent caspase-9 activation is necessary for antigen receptor-mediated effector caspase activation and apoptosis in WEHI 231 lymphoma cells. J. Immunol., 168(8):3902-3909.
[12]Hortobagyi, G.N., Ames, F.C., Buzdar, A.U., et al., 1988. Management of stage III primary breast cancer with primary chemotherapy, surgery, and radiation therapy. Cancer, 62(12):2507-2516.
[13]Huang, X.C., Wang, M., Wang, H.S., et al., 2014. Synthesis and antitumor activities of novel dipeptide derivatives derived from dehydroabietic acid. Bioorg. Med. Chem. Lett., 24(6):1511-1518.
[14]Jiang, X.G., 2014. Harnessing the immune system for the treatment of breast cancer. J. Zhejiang Univ.-Sci. B (Biomed. & Biotechnol.), 15(1):1-15.
[15]Khan, N., Mukhtar, H., 2007. Tea polyphenols for health promotion. Life Sci., 81(7):519-533.
[16]Li, L.L., Cao, W.Q., Zheng, W.J., et al., 2012. Ruthenium complexes containing 2,6-bis(benzimidazolyl)pyridine derivatives induce cancer cell apoptosis by triggering DNA damage-mediated p53 phosphorylation. Dalton Trans., 41(41):12766-12772.
[17]Li, T., Zhu, J., Guo, L., et al., 2013. Differential effects of polyphenols-enriched extracts from hawthorn fruit peels and fleshes on cell cycle and apoptosis in human MCF-7 breast carcinoma cells. Food Chem., 141(2):1008-1018.
[18]Liang, H.H., Huang, H.H., Kwok, K.C., 1999. Properties of tea-polyphenol-complexed bromelain. Food Res. Int., 32(8):545-551.
[19]Liu, H.X., Li, X.L., Dong, C.F., 2015. Epigenetic and metabolic regulation of breast cancer stem cells. J. Zhejiang Univ.-Sci. B (Biomed. & Biotechnol.), 16(1):10-17.
[20]Liu, S.M., Huang, H.H., 2015. Assessments of antioxidant effect of black tea extract and its rationals by erythrocyte haemolysis assay, plasma oxidation assay and cellular antioxidant activity (CAA) assay. J. Funct. Foods, 18(Part B):1095-1105.
[21]Lu, G., Xiao, H., You, H., et al., 2008. Synergistic inhibition of lung tumorigenesis by a combination of green tea polyphenols and atorvastatin. Clin. Cancer Res., 14(15):4981-4988.
[22]Luo, H.T., Tang, L.L., Tang, M., et al., 2006. Phase IIa chemoprevention trial of green tea polyphenols in high-risk individuals of liver cancer: modulation of urinary excretion of green tea polyphenols and 8-hydroxydeoxyguanosine. Carcinogenesis, 27(2):262-268.
[23]Pan, G.H., O'Rourke, K., Dixit, V.M., 1998. Caspase-9, Bcl-XL, and Apaf-1 form a ternary complex. J. Biol. Chem., 273(10):5841-5845.
[24]Pandey, M., Shukla, S., Gupta, S., 2010. Promoter demethylation and chromatin remodeling by green tea polyphenols leads to re-expression of GSTP1 in human prostate cancer cells. Int. J. Cancer, 126(11):2520-2533.
[25]Pianetti, S., Guo, S., Kavanagh, K.T., et al., 2002. Green tea polyphenol epigallocatechin-3 gallate inhibits Her-2/neu signaling, proliferation, and transformed phenotype of breast cancer cells. Cancer Res., 62(3):652-655.
[26]Quan, Z.W., Gu, J., Dong, P., et al., 2010. Reactive oxygen species-mediated endoplasmic reticulum stress and mitochondrial dysfunction contribute to cirsimaritin-induced apoptosis in human gallbladder carcinoma GBC-SD cells. Cancer Lett., 295(2):252-259.
[27]Radad, K., Rausch, W.D., Gille, G., 2006. Rotenone induces cell death in primary dopaminergic culture by increasing ROS production and inhibiting mitochondrial respiration. Neurochem. Int., 49(4):379-386.
[28]Rezaei, P.F., Fouladdel, S., Hassani, S., et al., 2012. Induction of apoptosis and cell cycle arrest by pericarp polyphenol-rich extract of Baneh in human colon carcinoma HT29 cells. Food Chem. Toxicol., 50(3-4):1054-1059.
[29]Rogalska, A., Koceva-Chyła, A., Jóźwiak, Z., 2008. Aclarubicin-induced ROS generation and collapse of mitochondrial membrane potential in human cancer cell lines. Chem. Biol. Interact., 176(1):58-70.
[30]Stewart, B.W., Wild, C.P., 2014. World Cancer Report 2014. World Health Organization, International Agency for Research on Cancer, Lyon, France.
[31]Strasser, A., O'Connor, L., Dixit, V.M., 2000. Apoptosis signaling. Annu. Rev. Biochem., 69:217-245.
[32]Sun, X.M., MacFarlane, M., Zhuang, J., et al., 1999. Distinct caspase cascades are initiated in receptor-mediated and chemical-induced apoptosis. J. Biol. Chem., 274(8):5053-5060.
[33]Thangapazham, R.L., Singh, A.K., Sharma, A., et al., 2007. Green tea polyphenols and its constituent epigallocatechin gallate inhibits proliferation of human breast cancer cells in vitro and in vivo. Cancer Lett., 245(1-2):232-241.
[34]Yang, C.S., Lambert, J.D., Sang, S., 2009. Antioxidative and anti-carcinogenic activities of tea polyphenols. Arch. Toxicol., 83(1):11-21.
[35]Zhang, J.Y., Wu, H.Y., Xia, X.K., et al., 2007. Anthracenedione derivative 1403P-3 induces apoptosis in KB and KBv200 cells via reactive oxygen species-independent mitochondrial pathway and death receptor pathway. Cancer Biol. Ther., 6(9):1409-1417.
Open peer comments: Debate/Discuss/Question/Opinion
<1>