Zahra Foroutan, Arrigo Francesco Giuseppe Cicero, Tannaz Jamialahmadi, Amirhossein Sahebkar
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引用次数: 0

摘要

坏死是一种新出现的程序性细胞死亡形式,其特点是细胞坏死,这是一种炎症性细胞死亡。坏死主要由与受体蛋白相互作用的特定介质启动,导致蛋白激酶 RIPK1 和 RIPK3 的激活。这些激酶传递死亡信号,并招募和磷酸化混合系激酶域样蛋白(MLKL),最终引发细胞死亡和坏死。姜黄素是从姜黄中提取的天然化合物,已被证明具有多种治疗功效,包括神经保护、抗代谢综合征、抗炎和抗癌作用。在这篇简明综述中,我们旨在根据最近的体内和体外研究,探讨姜黄素与坏死通路分子机制之间的关系。现有文献表明,姜黄素(主要是姜黄素)在组织损伤情况下可作为坏死抑制剂,而在癌细胞中则可作为坏死诱导剂。姜黄素对坏死的关键指标有明显的影响,突出了其加强疾病治疗的潜力。未来的研究应侧重于进一步研究姜黄的这一重要成分,以推进治疗方法的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Curcuminoids as natural modulators of necroptosis: therapeutic implications

Curcuminoids as natural modulators of necroptosis: therapeutic implications

Necroptosis is an emerging form of programmed cell death characterized by necrosis, an inflammatory type of cell death. Necroptosis is primarily initiated by specific mediators that interact with receptor proteins, leading to the activation of protein kinases RIPK1 and RIPK3. These kinases transmit death signals and recruit and phosphorylate mixed lineage kinase domain-like protein (MLKL), which ultimately triggers cell death and necroptosis. Curcuminoids, natural compounds derived from turmeric, have been shown to possess various therapeutic benefits, including neuroprotective, anti-metabolic syndrome, anti-inflammatory, and anti-cancer effects. In this concise overview, we aim to explore the relationship between curcuminoids and the molecular mechanisms of the necroptosis pathway based on recent in vivo and in vitro studies. The available literature indicates that curcuminoids, mainly curcumin, can act as inhibitors of necroptosis in tissue damage scenarios while serving as a necroptosis inducer in cancer cells. Curcuminoids significantly influence key indicators of necroptosis, highlighting their potential to enhance disease treatment. Future studies should focus on further investigating this important component of turmeric to advance therapeutic approaches.

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