α-生育酚琥珀酸酯作为癌症治疗剂的发现导致了潜在提高癌症治疗效果的方法的开发。

IF 6.8 4区 医学 Q1 NUTRITION & DIETETICS Journal of the American Nutrition Association Pub Date : 2023-11-01 Epub Date: 2023-02-03 DOI:10.1080/27697061.2023.2175389
Kedar N Prasad
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引用次数: 0

摘要

发现α-丁二酸丁二酯(α-TS)作为癌症治疗剂显著刺激了有或无肿瘤治疗剂对癌症细胞和正常细胞的研究。结果表明,α-TS治疗诱导癌症细胞凋亡,并以协同方式增强肿瘤治疗剂对肿瘤细胞的凋亡作用,而不影响正常细胞的生长。脂质体α-TS比α-TS更有效。有些肿瘤很难用化疗药物治疗,而有些则对这种治疗产生耐药性。使用纳米技术,证明了与化疗剂偶联的α-TS增强了细胞凋亡水平,并恢复了肿瘤细胞对该化疗剂的敏感性。α-TS单独或与治疗剂联合的作用机制包括:(a)抑制癌基因C-myc和H-ras的表达;(b) 许多基因表达水平的改变;(c) 胱天蛋白酶的激活;(d) 抑制血管生成;(e) 线粒体和溶酶体不稳定;(f) 抑制前列腺素E2(PGE2)的产生和PGE2介导的促炎反应;(g) survivin信号通路减少;和(h)肿瘤细胞表面CD47表达的减少,引起巨噬细胞吞噬活性的增强,导致肿瘤细胞的吞噬。尽管在细胞培养和动物模型中取得了令人印象深刻的结果,但尚未对抗这些疗法的人类癌症进行单独使用α-TS或与癌症治疗剂联合使用的研究。
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Discovery of Alpha-Tocopheryl Succinate as a Cancer Treatment Agent Led to the Development of Methods to Potentially Improve the Efficacy of Cancer Therapy.

The discovery of alpha-tocopheryl succinate (alpha-TS) as a cancer therapeutic agent markedly stimulated research with or without tumor therapeutic agents on cancer cells and normal cells. Results showed that alpha-TS treatment induced apoptosis in cancer cells and enhanced the apoptotic effects of tumor therapeutic agents on tumor cells in a synergistic manner without affecting the growth of normal cells. Liposomal alpha-TS was more effective than alpha-TS. Some tumors are difficult to treat with chemotherapeutic agents while some become resistant of such treatment. Using a nanotechnology technique, it was demonstrated that alpha-TS conjugated with a chemotherapeutic agent enhanced the levels of apoptosis and restored the sensitivity of tumor cells to that chemotherapeutic agent. The mechanisms of action of alpha-TS alone or in combination with therapeutic agents include the following: (a) inhibition of the expression of oncogenes C-myc and H-ras; (b) alterations in the levels of expression of numerous genes; (c) activation of caspases; (d) inhibition of angiogenesis; (e) destabilization of mitochondria and lysosomes; (f) inhibition of production of production of prostaglandin E2 (PGE2) and PGE2-mediated pro-inflammatory responses; (g) reduction of survivin signaling pathway; and (h) reduction of CD47 expression on the tumor cell surface causing enhancement of phagocytic activity of macrophages leading to engulfment of tumor cells. Despite impressive results in cell culture and in animal models, no studies with alpha-TS alone or in combination with cancer therapeutic agents in human cancer resistant to these therapies have been performed.

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