Jiang Shisheng, Huang Chaoming, Zheng Guodong, Yi Wei, Wu Bo, Tang Junyuan, Liu Xiawen, Huang Biyun, Wu Dan, Yan Tingdong, Li Mingxi, Wan Chunpeng, Cai Yi
Key Laboratory of Molecular Target & Clinical Pharmacology, The State & NMPA Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences, Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
School of Pharmacy, Nantong University, Nantong, China.
Front Nutr. 2022 Apr 25;9:851972. doi: 10.3389/fnut.2022.851972. eCollection 2022.
Epigallocatechin-3-gallate (EGCG), a frequently studied catechin in green tea, has been shown involved in the anti-proliferation and apoptosis of human nasopharyngeal carcinoma (NPC) cells. However, the underlying molecular mechanism of the apoptotic effects of EGCG has not been fully investigated. Recent literature emphasized the importance of Sirtuin 1 (SIRT1), an NAD-dependent protein deacetylase, in regulating cellular stress responses, survival, and organismal lifespan. Herein, the study showed that EGCG could significantly inhibit cell proliferation and promote apoptosis of 2 NPC (CNE-2 and 5-8F) cell lines. Moreover, it was also found that SIRT1 is down-regulated by EGCG, and the SIRT1-p53 signaling pathway participates in the effects of EGCG on CNE-2 and 5-8 F cells. Taken together, the findings of this study provided evidence that EGCG could inhibit the growth of NPC cell lines and is linked with the inhibition of the SIRT1-p53 signaling pathway, suggesting the therapeutic potential of EGCG in human NPC.
表没食子儿茶素-3-没食子酸酯(EGCG)是绿茶中一种经常被研究的儿茶素,已被证明参与人类鼻咽癌(NPC)细胞的抗增殖和凋亡过程。然而,EGCG凋亡作用的潜在分子机制尚未得到充分研究。最近的文献强调了沉默调节蛋白1(SIRT1)(一种NAD依赖性蛋白脱乙酰酶)在调节细胞应激反应、生存和生物体寿命方面的重要性。在此,该研究表明EGCG可显著抑制两种NPC(CNE-2和5-8F)细胞系的细胞增殖并促进其凋亡。此外,还发现EGCG可下调SIRT1,且SIRT1-p53信号通路参与EGCG对CNE-2和5-8F细胞的作用。综上所述,本研究结果提供了证据表明EGCG可抑制NPC细胞系的生长,并与SIRT1-p53信号通路的抑制有关,提示EGCG在人类鼻咽癌治疗中的潜在应用价值。