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揭示表没食子儿茶素没食子酸酯和酒石酸坦度螺酮联合对人三阴性乳腺癌细胞生长的影响。

Shining a Light on the Effects of the Combination of (-)-Epigallocatechin-3-gallate and Tapentadol on the Growth of Human Triple-negative Breast Cancer Cells.

机构信息

Division of Anesthesia and Pain Medicine, National Institute of Tumors, G. Pascale Foundation, Naples, Italy

Division of Anesthesia and Pain Medicine, National Institute of Tumors, G. Pascale Foundation, Naples, Italy.

出版信息

In Vivo. 2019 Sep-Oct;33(5):1463-1468. doi: 10.21873/invivo.11625.

Abstract

BACKGROUND/AIM: Breast cancer is characterized by a high rate of mortality and is considered one of the deadliest types of cancer. It is of note that (-)-epigallocatechin-3-gallate (EGCG), the principal catechin of green tea, is able to hinder the growth of MDA-MB-231 breast cancer cells by influencing different signaling pathways, including apoptosis. Furthermore, EGCG is also used in the treatment of bone cancer pain. Tapentadol, an opioid drug acting at the level of noradrenaline (norepinephrine) reuptake inhibition and μ-opioid receptor, is able to modulate bone cancer pain and influence cancer cell viability by regulating apoptosis.

MATERIALS AND METHODS

In vitro assays were performed on triple-negative MDA-MB-231 cells treated with tapentadol (1, 5, 10, 20, 40 and 80 μg/ml) and EGCG (1, 10, 20, 40, 80, 160 μmol/l), alone and in combination. The effects of EGCG and TAP on viability were determined by wound-healing and MTT assays, while cell migration was assessed by transwell migration.

RESULTS

Cell proliferation, viability and apoptosis of MDA-MB-231 cells were impaired by the combination of EGCG and tapentadol. Specifically, our data show that EGCG and TAP reduced the proliferation of MDA-MB-231 cells by impairing cell-cycle progression (p<0.05). These findings suggest that the combination of these substances may represent a new strategy for the treatment of patients suffering from triple-negative breast cancer.

摘要

背景/目的:乳腺癌具有较高的死亡率,被认为是最致命的癌症之一。值得注意的是,绿茶中的主要儿茶素 (-)-表没食子儿茶素-3-没食子酸酯 (EGCG) 通过影响包括细胞凋亡在内的不同信号通路,能够抑制 MDA-MB-231 乳腺癌细胞的生长。此外,EGCG 还用于治疗骨癌疼痛。曲马多是一种作用于去甲肾上腺素(去甲肾上腺素)再摄取抑制和 μ 阿片受体的阿片类药物,能够通过调节细胞凋亡来调节骨癌疼痛并影响癌细胞活力。

材料和方法

在体外实验中,用曲马多(1、5、10、20、40 和 80 μg/ml)和 EGCG(1、10、20、40、80、160 μmol/l)单独或联合处理三阴性 MDA-MB-231 细胞,进行体外检测。用划痕愈合和 MTT 试验测定 EGCG 和 TAP 对细胞活力的影响,用 Transwell 迁移试验评估细胞迁移。

结果

EGCG 和曲马多联合作用可损害 MDA-MB-231 细胞的增殖、活力和凋亡。具体而言,我们的数据表明,EGCG 和 TAP 通过损害细胞周期进程来降低 MDA-MB-231 细胞的增殖(p<0.05)。这些发现表明,这些物质的联合使用可能代表治疗三阴性乳腺癌患者的一种新策略。

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