富多酚提取物对肿瘤细胞和正常细胞的不同作用机制

C. Branco, T. Rodrigues, É. Lima, M. Salvador
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引用次数: 6

摘要

与正常细胞相比,癌细胞表现出不同的代谢。多种分子机制汇聚在一起改变细胞代谢,其中一些包括代谢重编程过程,它为肿瘤细胞的能量产生、生长和增殖提供了优势。肿瘤能量的产生主要依赖于葡萄糖驱动的糖酵解(Warburg效应),但也通过脂肪酸和谷氨酰胺代谢发生。在当前癌症治疗面临的挑战中,肿瘤细胞的耐药性和抗癌药物的缺乏选择性是突出的问题。已经证明,多酚能够对正常细胞和肿瘤细胞发挥不同的作用。然而,这些行为的确切机制尚不完全清楚。在我们之前的研究中,我们发现一种富含多酚的紫砂提取物(PE)具有选择性抑制人喉部HEp-2癌细胞增殖的能力,而对正常上皮细胞的细胞毒性很小。我们假设PE的作用是通过逆转癌细胞的“Warburg效应”和抑制线粒体电子传递链复合体I的活性以及这些细胞上ATP的消耗而发生的。在本研究重点中,我们将讨论PE对线粒体代谢的影响及其在线粒体sirtuin 3 (SIRT3)对肿瘤(HEp-2)和正常(HEK-293)细胞的调节中的可能作用,这可能有助于阐明多酚所表现出的肿瘤选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polyphenols-rich extract from Araucaria angustifolia: Differential mechanisms on cancer and normal cells
Cancer cells present differential metabolism compared to normal cells. Multiple molecular mechanisms converge to alter cellular metabolism, and some of these include a process of metabolic reprogramming which provides advantages to tumor cells in energy generation, growth and proliferation. Tumor energy production is basically dependent on glucose driven to glycolysis (Warburg effect), but it also happens by means of fatty acids and glutamine metabolism. Among the current challenges in cancer therapy, the tumor cell resistance and the absence of selectivity of anti-cancer agents stand out. It has been already shown that polyphenols are able to exert differential effects on normal and tumor cells. However, the exact mechanisms of these actions are not fully understood. In our previous study, we showed that a polyphenols-rich extract (PE) from Araucaria angustifolia held a selective capacity to inhibit the proliferation of human larynx HEp-2 cancer cells with minimal cytotoxicity to normal epithelial cells. We hypothesized that the effect presented by PE have happened by reversing the “Warburg effect” on cancer cells and inhibiting the mitochondrial electron transport chain complex I activity along with ATP depletion on these cells. In this research highlight we will discuss the effects of the PE on mitochondrial metabolism and their possible role in the modulation of mitochondrial sirtuin 3 (SIRT3) on tumor (HEp-2) and normal (HEK-293) cells, which may help to clarify the tumor selectivity exhibited by polyphenols.
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