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神经酰胺在癌症治疗中的治疗潜力。

Therapeutic Potential of Ceramide in Cancer Treatment.

作者信息

Wang Weiyuan, Prince Bert F, Thorpe Alexander J, Brown Timothy J, Barth Brian M

机构信息

Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta GA 30322 USA.

Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham NH 03824 USA.

出版信息

J Cancer Res Oncobiol. 2024;4(1). Epub 2024 Sep 30.

PMID:40384804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12083856/
Abstract

Ceramides are a family of wax-like lipids that fall under the broader category of sphingolipids. A ceramide is composed of a sphingosine side chain coupled to a fatty acid via an amide linkage. Distinct from complex sphingolipids, the head of ceramide is a simple alcohol rather than a phosphate, phosphocholine, sugar, or more. The fatty acid chains of ceramide can also vary in chain length and degree of saturation. The degree of saturation may determine the biological activity of the ceramide species. Ceramides are highly abundant within the cell membrane of eukaryotic cells and are appreciated for their structural roles in these cells. Moreover, ceramides are well-known for their biological activity including as regulators of apoptosis, senescence, the cell cycle, and differentiation. This review discusses pathways of ceramide, roles of ceramide in various diseases, targeting ceramide metabolism in the treatment of cancer, as well as ceramide-delivering nanotechnologies.

摘要

神经酰胺是一类蜡样脂质,属于更广泛的鞘脂类。神经酰胺由一个鞘氨醇侧链通过酰胺键与脂肪酸相连组成。与复杂鞘脂不同,神经酰胺的头部是一种简单的醇,而不是磷酸、磷酸胆碱、糖等。神经酰胺的脂肪酸链在链长和饱和度上也可能有所不同。饱和度可能决定神经酰胺种类的生物活性。神经酰胺在真核细胞的细胞膜中含量非常丰富,并因其在这些细胞中的结构作用而受到重视。此外,神经酰胺以其生物活性而闻名,包括作为细胞凋亡、衰老、细胞周期和分化的调节剂。本文综述了神经酰胺的代谢途径、神经酰胺在各种疾病中的作用、针对神经酰胺代谢治疗癌症以及神经酰胺递送纳米技术。

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Therapeutic Potential of Ceramide in Cancer Treatment.神经酰胺在癌症治疗中的治疗潜力。
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An overview of sphingolipid metabolism: from synthesis to breakdown.鞘脂代谢概述:从合成到分解。
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Sphingolipids and cancer: ceramide and sphingosine-1-phosphate in the regulation of cell death and drug resistance.鞘脂类和癌症:细胞死亡和耐药性调控中的神经酰胺和 1-磷酸鞘氨醇。
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The sphingolipid salvage pathway in ceramide metabolism and signaling.神经酰胺代谢与信号传导中的鞘脂补救途径。
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Cancer treatment strategies targeting sphingolipid metabolism.靶向鞘脂代谢的癌症治疗策略。
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本文引用的文献

1
Unraveling Atopic Dermatitis: Insights into Pathophysiology, Therapeutic Advances, and Future Perspectives.解析特应性皮炎:对病理生理学、治疗进展及未来展望的见解
Cells. 2024 Feb 28;13(5):425. doi: 10.3390/cells13050425.
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A phase I study of the ceramide nanoliposome in patients with advanced solid tumors.一项关于晚期实体瘤患者的神经酰胺纳米脂质体的 I 期研究。
Cancer Chemother Pharmacol. 2024 Jan;93(1):23-29. doi: 10.1007/s00280-023-04588-7. Epub 2023 Sep 22.
3
Ceramide nanoliposomes augment the efficacy of venetoclax and cytarabine in models of acute myeloid leukemia.
神经酰胺纳米脂质体增强 venetoclax 和阿糖胞苷在急性髓系白血病模型中的疗效。
FASEB J. 2022 Oct;36(10):e22514. doi: 10.1096/fj.202200765R.
4
Ceramide: improving Bcl-2 inhibitor therapy.神经酰胺:改善Bcl-2抑制剂疗法。
Blood. 2022 Jun 30;139(26):3676-3678. doi: 10.1182/blood.2022016608.
5
Atopic Dermatitis: The Fate of the Fat.特应性皮炎:脂肪的命运。
Int J Mol Sci. 2022 Feb 14;23(4):2121. doi: 10.3390/ijms23042121.
6
Sphingolipids as Regulators of Neuro-Inflammation and NADPH Oxidase 2.鞘脂类作为神经炎症和 NADPH 氧化酶 2 的调节剂。
Neuromolecular Med. 2021 Mar;23(1):25-46. doi: 10.1007/s12017-021-08646-2. Epub 2021 Feb 5.
7
Developing new ceramide analogs and identifying novel sphingolipid-controlled genes against a virus-associated lymphoma.研发新型神经酰胺类似物并鉴定新型受鞘脂调控的与病毒相关的淋巴瘤相关基因。
Blood. 2020 Nov 5;136(19):2175-2187. doi: 10.1182/blood.2020005569.
8
C-ceramide Inhibits the Motility of Anaplastic Thyroid Carcinoma Cells.C-神经酰胺抑制间变性甲状腺癌细胞的运动能力。
Yonago Acta Med. 2020 Mar 23;63(2):95-98. doi: 10.33160/yam.2020.05.001. eCollection 2020 May.
9
Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis.鼠表皮神经酰胺合成酶 4 是皮肤屏障稳态的关键调节因子。
J Invest Dermatol. 2020 Oct;140(10):1927-1937.e5. doi: 10.1016/j.jid.2020.02.006. Epub 2020 Feb 22.
10
Glucosylceramide synthase maintains influenza virus entry and infection.葡萄糖神经酰胺合酶维持流感病毒的进入和感染。
PLoS One. 2020 Feb 7;15(2):e0228735. doi: 10.1371/journal.pone.0228735. eCollection 2020.