Faculty of Applied Health Sciences, Brock University, St. Catharines, ON L2S 3A1, Canada.
Centre for Bone and Muscle Health, Brock University, St. Catharines, ON L2S 3A1, Canada.
Molecules. 2021 Feb 13;26(4):987. doi: 10.3390/molecules26040987.
Cancer is a disease characterized by aberrant proliferative and apoptotic signaling pathways, leading to uncontrolled proliferation of cancer cells combined with enhanced survival and evasion of cell death. Current treatment strategies are sometimes ineffective in eradicating more aggressive, metastatic forms of cancer, indicating the need to develop novel therapeutics targeting signaling pathways which are essential for cancer progression. Historically, plant-derived compounds have been utilized in the production of pharmaceuticals and chemotherapeutic compounds for the treatment of cancer, including paclitaxel and docetaxel. Theaflavins, phenolic components present in black tea, have demonstrated anti-cancer potential in cell cultures in vitro and in animal studies in vivo. Theaflavins have been shown to inhibit proliferation, survival, and migration of many cancer cellswhile promoting apoptosis. Treatment with theaflavins has been associated with increased levels of cleaved poly (ADP-ribose) polymerase (PARP) and cleaved caspases-3, -7, -8, and -9, all markers of apoptosis, and increased expression of the proapoptotic marker Bcl-2-associated X protein (Bax) and concomitant reduction in the antiapoptotic marker B-cell lymphoma 2 (Bcl-2). Additionally, theaflavin treatment reduced phosphorylated Akt, phosphorylated mechanistic target of rapamycin (mTOR), phosphatidylinositol 3-kinase (PI3K), and c-Myc levels with increased expression of the tumour suppressor p53. This review summarizes the current in vitro and in vivo evidence available investigating the anti-cancer effects of theaflavins across various cancer cell lines and animal models.
癌症是一种以异常增殖和凋亡信号通路为特征的疾病,导致癌细胞的不受控制增殖,同时增强了细胞的存活和逃避细胞死亡的能力。目前的治疗策略在消除更具侵袭性、转移性的癌症方面有时并不有效,这表明需要开发针对对癌症进展至关重要的信号通路的新型治疗方法。历史上,植物衍生的化合物已被用于生产用于治疗癌症的药物和化疗化合物,包括紫杉醇和多西紫杉醇。茶黄素是红茶中的酚类成分,已在体外细胞培养和体内动物研究中显示出抗癌潜力。茶黄素已被证明能抑制许多癌细胞的增殖、存活和迁移,同时促进细胞凋亡。用茶黄素治疗与增加的切割多聚(ADP-核糖)聚合酶(PARP)和切割半胱天冬酶-3、-7、-8 和 -9 的水平有关,所有这些都是细胞凋亡的标志物,以及促凋亡标志物 Bcl-2 相关 X 蛋白(Bax)的表达增加和抗凋亡标志物 B 细胞淋巴瘤 2(Bcl-2)的相应减少。此外,茶黄素治疗降低了磷酸化 Akt、磷酸化雷帕霉素(mTOR)靶蛋白(mTOR)、磷脂酰肌醇 3-激酶(PI3K)和 c-Myc 的水平,同时增加了肿瘤抑制因子 p53 的表达。本综述总结了目前关于茶黄素在各种癌细胞系和动物模型中的抗癌作用的体外和体内证据。