[配方:见正文]-谷甾醇的抗癌潜力:机制和治疗前景的综合探索。

IF 5.5
The American journal of Chinese medicine Pub Date : 2025-01-01 Epub Date: 2025-06-17 DOI:10.1142/S0192415X2550048X
Yuzhe Zhang, Chunjiao Yang, Junhan Guo, Lirong Yan, Yanke Li, Ye Zhang
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引用次数: 0

摘要

本文全面研究了β-谷甾醇的抗癌机制和治疗潜力,这是一种天然存在于多种植物中的植物甾醇。β-谷甾醇通过诱导细胞凋亡、阻滞细胞周期进程、抑制细胞增殖、侵袭和迁移等多种生物学途径抑制肿瘤生长和转移。我们强调了β-谷甾醇发挥其作用的关键机制,如调节凋亡相关的信号通路,如Bcl-2家族蛋白和活性氧的产生。此外,还讨论了β-谷甾醇在破坏上皮-间质转化中的作用及其对肿瘤代谢的影响,特别是在胆固醇和葡萄糖调节方面的影响。本文还探讨了β-谷甾醇提高化疗敏感性的潜力,使其成为癌症治疗中有希望的辅助药物。此外,我们结合文献计量学分析和网络药理学方法来确定β-谷甾醇影响的潜在治疗靶点和途径,为其多方面的抗癌活性提供新的见解。这些发现强调了β-谷甾醇作为一种新型抗癌药物的潜力,值得进一步的研究和临床研究以优化其未来的治疗应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticancer Potential of [Formula: see text]-Sitosterol: A Comprehensive Exploration of Mechanisms and Therapeutic Prospects.

This paper comprehensively examines the anticancer mechanisms and therapeutic potential of β-sitosterol, a naturally occurring phytosterol found in various plants. β-Sitosterol has shown significant efficacy in inhibiting tumor growth and metastasis through various biological pathways, including inducing apoptosis, arresting cell cycle progression, and suppressing cell proliferation, invasion, and migration. We highlight the key mechanisms by which β-sitosterol exerts its effects, such as modulating apoptosis-related signaling pathways like those of the Bcl-2 family proteins and reactive oxygen species production. Furthermore, β-sitosterol's role in disrupting the epithelial-mesenchymal transition and its impact on tumor metabolism, particularly in cholesterol and glucose regulation, are discussed. The article also explores the potential of β-sitosterol to enhance chemotherapy sensitivity, making it a promising adjunct in cancer treatment. Additionally, we incorporate a bibliometric analysis and network pharmacology approach to identify potential therapeutic targets and pathways influenced by β-sitosterol, providing new insights into its multifaceted anticancer activities. These findings underscore the potential of β-sitosterol as a novel anticancer agent, warranting further research and clinical investigation to optimize its future therapeutic application.

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