In Vitro Antithrombotic, Antitumor and Antiangiogenic Activities of Green Tea Polyphenols and Its Main Constituent Epigallocatechin-3-gallate

被引:9
作者
da Luz, Jefferson Romaryo Duarte [1 ,2 ]
Lopez, Jorge A. [1 ,2 ]
Ferreira, Macelia Pinheiro [2 ]
de Sousa, Rubiamara Mauricio [2 ,3 ]
Victor e Silva, Saulo [2 ,4 ]
das Gracas Almeida, Maria [2 ,3 ,4 ]
Araujo-Silva, Gabriel [1 ]
机构
[1] State Univ Amapa UEAP, Organ Chem & Biochem Lab, Ave Presidente Vargas S-N Ctr, BR-68900070 Macapa, AP, Brazil
[2] Univ Fed Rio Grande do Norte, Hlth Sci Ctr, Dept Clin & Toxicol Anal DACT, Multidisciplinary Res Lab, R Gen Gustavo Cordeiro de Farias S-N, BR-59012570 Natal, RN, Brazil
[3] Univ Fed Rio Grande do Norte, Hlth Sci Ctr, Postgrad Program Hlth Sci, R Gen Gustavo Cordeiro de Farias S-N, BR-59012570 Natal, RN, Brazil
[4] Univ Fed Rio Grande do Norte, Hlth Sci Ctr, Postgrad Program Pharmaceut Sci, R Gen Gustavo Cordeiro de Farias S-N, BR-59012570 Natal, RN, Brazil
关键词
melanoma; cancer; anticoagulant; apoptosis; toxicity; green tea; DOWN-REGULATION; BIOACTIVE COMPONENTS; MELANIN SYNTHESIS; CANCER CELLS; EGCG; APOPTOSIS; EXTRACT; VEGF; (-)-EPIGALLOCATECHIN-3-GALLATE; MELANOGENESIS;
D O I
10.3390/pr11010076
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The balance between embolic risk and bleeding represents a clinical challenge in cancer patient treatment, encouraging studies on adjuvant oncologic treatments. Thereby, this study evaluated the in vitro effect of green tea extract (GTE) and epigallocatechin-3-gallate (EGCG) on hemostasis modulation and the antineoplastic effect on melanoma cells (B16-F10) by applying platelet aggregation, angiogenesis and viability cell assays. The results displayed a significant platelet antiaggregant effect, corresponding to 50 and 80% for the extract and EGCG, respectively, compared to the negative control. Furthermore, both GTE and EGCG exhibited antitumor effects by reducing melanoma cell growth by 25 and 50%, respectively, verified by cellular apoptosis. Regarding angiogenesis, these substances inhibited blood vessel formation, reaching about 25% and 99% for GTE and EGCG at 100 mu g/mL, respectively. Moreover, TNF-alpha cell stimulation evidenced VEGF and IL-8 secretion inhibition at 55 and 20% with GTE, while EGCG promoted an inhibition around 78% for both VEGF and IL-8. The results indicate the promising performance of GTE and EGCG as an option for treating cancer and its side effects. Nonetheless, further studies are required to elucidate their action mechanism on clotting, cell death and angiogenesis.
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页数:17
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