红茶抑制侵袭性并逆转 TNF-α 诱导的人类恶性黑色素瘤细胞侵袭性和细胞干性

IF 4.4 3区 医学 Q2 ENVIRONMENTAL SCIENCES
Chin-Yin Lin,Shu-Chen Chu,Yih-Shou Hsieh,Wen-Yi Tsai,Pei-Ni Chen
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引用次数: 0

摘要

侵袭性和上皮-间质转化(EMT)是转移性疾病的主要模式,也是人类恶性黑色素瘤细胞与癌症相关的主要致死原因。茶叶及其提取物可降低几种癌症的患病风险,并具有抗炎和抗氧化的生物效应。然而,人们对红茶乙醇提取物(BTEE)在人类黑色素瘤中的抗EMT和抗癌干效应仍知之甚少。本研究评估了红茶乙醇提取物在人类 A 375 和 A2058 黑色素瘤细胞中降低侵袭性、EMT 和癌症干性的作用。BTEE 通过抑制 p-FAK 信号通路抑制了 u-PA 活性、迁移和侵袭性。BTEE 通过下调 β-catenin、N-cadherin、fibronectin、vimentin 和 Twist-1 的表达来影响 EMT。BTEE 还能降低肿瘤坏死因子-α(TNF-α)在体外诱导的侵袭性和癌症干性特征。裸鼠异种移植模型中黑色素瘤的生长表明,BTEE 可抑制 A 375 肿瘤在体内的生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Black Tea Suppresses Invasiveness and Reverses TNF-α-Induced Invasiveness and Cell Stemness in Human Malignant Melanoma Cells.
Invasiveness and epithelial-mesenchymal transition (EMT) are main patterns of metastatic disease, which is the major cause cancer-related mortality in human malignant melanoma cells. Tea and its consumption extract are associated with a lower risk of several types of cancer and have anti-inflammatory and antioxidative biological effects. However, the anti-EMT and anti-cancer stemness effect of black tea ethanol extracts (BTEE) in human melanoma remain poorly understood. In this study, the effects of BTEE-reduced invasiveness, EMT, and cancer stemness were evaluated in human A 375 and A2058 melanoma cells. BTEE inhibited the activity of u-PA, migration, and invasiveness by repressing p-FAK signaling pathway. BTEE affected the EMT by downregulating the expression of β-catenin, N-cadherin, fibronectin, vimentin, and Twist-1. BTEE also reduced tumor necrosis factor-alpha (TNF-α)-induced invasiveness and cancer stemness characteristics in vitro. The growth of melanoma in nude mice xenograft model showed that BTEE suppressed A 375 tumor growth in vivo.
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来源期刊
Environmental Toxicology
Environmental Toxicology 环境科学-毒理学
CiteScore
7.10
自引率
8.90%
发文量
261
审稿时长
4.5 months
期刊介绍: The journal publishes in the areas of toxicity and toxicology of environmental pollutants in air, dust, sediment, soil and water, and natural toxins in the environment.Of particular interest are: Toxic or biologically disruptive impacts of anthropogenic chemicals such as pharmaceuticals, industrial organics, agricultural chemicals, and by-products such as chlorinated compounds from water disinfection and waste incineration; Natural toxins and their impacts; Biotransformation and metabolism of toxigenic compounds, food chains for toxin accumulation or biodegradation; Assays of toxicity, endocrine disruption, mutagenicity, carcinogenicity, ecosystem impact and health hazard; Environmental and public health risk assessment, environmental guidelines, environmental policy for toxicants.
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