Suppr超能文献

乙酰辅酶 A 在癌症中的代谢。

Acetyl-CoA metabolism in cancer.

机构信息

Program in Molecular Medicine, UMass Chan Medical School, Worcester, MA, USA.

Department of Cancer Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

出版信息

Nat Rev Cancer. 2023 Mar;23(3):156-172. doi: 10.1038/s41568-022-00543-5. Epub 2023 Jan 19.

Abstract

Few metabolites can claim a more central and versatile role in cell metabolism than acetyl coenzyme A (acetyl-CoA). Acetyl-CoA is produced during nutrient catabolism to fuel the tricarboxylic acid cycle and is the essential building block for fatty acid and isoprenoid biosynthesis. It also functions as a signalling metabolite as the substrate for lysine acetylation reactions, enabling the modulation of protein functions in response to acetyl-CoA availability. Recent years have seen exciting advances in our understanding of acetyl-CoA metabolism in normal physiology and in cancer, buoyed by new mouse models, in vivo stable-isotope tracing approaches and improved methods for measuring acetyl-CoA, including in specific subcellular compartments. Efforts to target acetyl-CoA metabolic enzymes are also advancing, with one therapeutic agent targeting acetyl-CoA synthesis receiving approval from the US Food and Drug Administration. In this Review, we give an overview of the regulation and cancer relevance of major metabolic pathways in which acetyl-CoA participates. We further discuss recent advances in understanding acetyl-CoA metabolism in normal tissues and tumours and the potential for targeting these pathways therapeutically. We conclude with a commentary on emerging nodes of acetyl-CoA metabolism that may impact cancer biology.

摘要

在细胞代谢中,很少有代谢物能像乙酰辅酶 A(acetyl-CoA)那样具有更核心和多样化的作用。乙酰辅酶 A 在营养物质分解代谢过程中产生,为三羧酸循环提供燃料,是脂肪酸和异戊二烯生物合成的必需结构单元。它还作为一种信号代谢物,作为赖氨酸乙酰化反应的底物,使蛋白质功能能够根据乙酰辅酶 A 的可用性进行调节。近年来,新的小鼠模型、体内稳定同位素示踪方法以及改进的乙酰辅酶 A 测量方法(包括在特定的亚细胞隔室中)的出现,推动了我们对正常生理和癌症中乙酰辅酶 A 代谢的理解取得了令人兴奋的进展。针对乙酰辅酶 A 代谢酶的靶向治疗也在取得进展,一种针对乙酰辅酶 A 合成的治疗药物已获得美国食品和药物管理局的批准。在这篇综述中,我们概述了乙酰辅酶 A 参与的主要代谢途径的调节和与癌症的相关性。我们进一步讨论了近年来对正常组织和肿瘤中乙酰辅酶 A 代谢的理解的进展,以及针对这些途径进行治疗的潜力。最后,我们对可能影响癌症生物学的新兴乙酰辅酶 A 代谢节点进行了评论。

相似文献

1
Acetyl-CoA metabolism in cancer.
Nat Rev Cancer. 2023 Mar;23(3):156-172. doi: 10.1038/s41568-022-00543-5. Epub 2023 Jan 19.
2
Acetyl-CoA metabolism as a therapeutic target for cancer.
Biomed Pharmacother. 2023 Dec;168:115741. doi: 10.1016/j.biopha.2023.115741. Epub 2023 Oct 19.
3
Compartmentalised acyl-CoA metabolism and roles in chromatin regulation.
Mol Metab. 2020 Aug;38:100941. doi: 10.1016/j.molmet.2020.01.005. Epub 2020 Feb 14.
4
Intracellular Citrate/acetyl-CoA flux and endoplasmic reticulum acetylation: Connectivity is the answer.
Mol Metab. 2023 Jan;67:101653. doi: 10.1016/j.molmet.2022.101653. Epub 2022 Dec 10.
5
Crosstalk between cellular metabolism and histone acetylation.
Methods Enzymol. 2019;626:1-21. doi: 10.1016/bs.mie.2019.07.013. Epub 2019 Aug 12.
6
Acetyl-CoA and the regulation of metabolism: mechanisms and consequences.
Curr Opin Cell Biol. 2015 Apr;33:125-31. doi: 10.1016/j.ceb.2015.02.003. Epub 2015 Feb 20.
8
Protein acetylation and acetyl coenzyme a metabolism in budding yeast.
Eukaryot Cell. 2014 Dec;13(12):1472-83. doi: 10.1128/EC.00189-14. Epub 2014 Oct 17.
10
Subcellular metabolic pathway kinetics are revealed by correcting for artifactual post harvest metabolism.
Mol Metab. 2019 Dec;30:61-71. doi: 10.1016/j.molmet.2019.09.004. Epub 2019 Sep 27.

引用本文的文献

2
Protein lipoylation in cancer: metabolic reprogramming and therapeutic potential.
Cell Death Discov. 2025 Sep 2;11(1):420. doi: 10.1038/s41420-025-02718-z.
6
Biochemistry and regulation of histone lysine L-lactylation.
Nat Rev Mol Cell Biol. 2025 Aug 19. doi: 10.1038/s41580-025-00876-7.
8
Metabolism and epigenetics in cancer: toward personalized treatment.
Front Endocrinol (Lausanne). 2025 Jul 25;16:1530578. doi: 10.3389/fendo.2025.1530578. eCollection 2025.
10
ACLY inhibition promotes tumour immunity and suppresses liver cancer.
Nature. 2025 Jul 30. doi: 10.1038/s41586-025-09297-0.

本文引用的文献

1
Adipocyte mesenchymal transition contributes to mammary tumor progression.
Cell Rep. 2022 Sep 13;40(11):111362. doi: 10.1016/j.celrep.2022.111362.
3
Brown-fat-mediated tumour suppression by cold-altered global metabolism.
Nature. 2022 Aug;608(7922):421-428. doi: 10.1038/s41586-022-05030-3. Epub 2022 Aug 3.
4
Inhibition of ATP-citrate lyase improves NASH, liver fibrosis, and dyslipidemia.
Cell Metab. 2022 Jun 7;34(6):919-936.e8. doi: 10.1016/j.cmet.2022.05.004.
5
Intracellular Acetyl CoA Potentiates the Therapeutic Efficacy of Antitumor CD8+ T Cells.
Cancer Res. 2022 Jul 18;82(14):2640-2655. doi: 10.1158/0008-5472.CAN-21-4052.
6
NAFLD-related hepatocellular carcinoma: The growing challenge.
Hepatology. 2023 Jan 1;77(1):323-338. doi: 10.1002/hep.32542. Epub 2022 Nov 8.
7
USP22 regulates lipidome accumulation by stabilizing PPARγ in hepatocellular carcinoma.
Nat Commun. 2022 Apr 21;13(1):2187. doi: 10.1038/s41467-022-29846-9.
8
Targeting ferroptosis as a vulnerability in cancer.
Nat Rev Cancer. 2022 Jul;22(7):381-396. doi: 10.1038/s41568-022-00459-0. Epub 2022 Mar 25.
10
O-GlcNAc transferase regulates glioblastoma acetate metabolism via regulation of CDK5-dependent ACSS2 phosphorylation.
Oncogene. 2022 Apr;41(14):2122-2136. doi: 10.1038/s41388-022-02237-6. Epub 2022 Feb 22.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验