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癌症中的代谢改变:能量途径和治疗靶点的新见解。

Altered metabolism in cancer: insights into energy pathways and therapeutic targets.

机构信息

Department of Oral and Maxillofacial Surgery, Center of Stomatology, Xiangya Hospital, Central South University, Changsha, China.

Institute of Oral Precancerous Lesions, Central South University, Changsha, China.

出版信息

Mol Cancer. 2024 Sep 18;23(1):203. doi: 10.1186/s12943-024-02119-3.


DOI:10.1186/s12943-024-02119-3
PMID:39294640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11409553/
Abstract

Cancer cells undergo significant metabolic reprogramming to support their rapid growth and survival. This study examines important metabolic pathways like glycolysis, oxidative phosphorylation, glutaminolysis, and lipid metabolism, focusing on how they are regulated and their contributions to the development of tumors. The interplay between oncogenes, tumor suppressors, epigenetic modifications, and the tumor microenvironment in modulating these pathways is examined. Furthermore, we discuss the therapeutic potential of targeting cancer metabolism, presenting inhibitors of glycolysis, glutaminolysis, the TCA cycle, fatty acid oxidation, LDH, and glucose transport, alongside emerging strategies targeting oxidative phosphorylation and lipid synthesis. Despite the promise, challenges such as metabolic plasticity and the need for combination therapies and robust biomarkers persist, underscoring the necessity for continued research in this dynamic field.

摘要

癌细胞经历了显著的代谢重编程,以支持其快速生长和存活。本研究检查了重要的代谢途径,如糖酵解、氧化磷酸化、谷氨酰胺分解和脂代谢,重点关注它们是如何被调节的,以及它们对肿瘤发展的贡献。还研究了癌基因、肿瘤抑制因子、表观遗传修饰和肿瘤微环境在调节这些途径中的相互作用。此外,我们还讨论了针对癌症代谢的治疗潜力,提出了针对糖酵解、谷氨酰胺分解、三羧酸循环、脂肪酸氧化、LDH 和葡萄糖转运的抑制剂,以及针对氧化磷酸化和脂质合成的新兴策略。尽管前景广阔,但代谢可塑性和联合治疗以及稳健生物标志物的需求等挑战仍然存在,这突显了在这个充满活力的领域继续研究的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/37046a1d866d/12943_2024_2119_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/d855fe05c265/12943_2024_2119_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/e9ae514e51f5/12943_2024_2119_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/ad2801e096ed/12943_2024_2119_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/98da185f5dd3/12943_2024_2119_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/11b0d01abe65/12943_2024_2119_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/37046a1d866d/12943_2024_2119_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/d855fe05c265/12943_2024_2119_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/e9ae514e51f5/12943_2024_2119_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/ad2801e096ed/12943_2024_2119_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/98da185f5dd3/12943_2024_2119_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/11b0d01abe65/12943_2024_2119_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd8b/11409553/37046a1d866d/12943_2024_2119_Fig6_HTML.jpg

相似文献

[1]
Altered metabolism in cancer: insights into energy pathways and therapeutic targets.

Mol Cancer. 2024-9-18

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
Dysregulation of glucose transport, glycolysis, TCA cycle and glutaminolysis by oncogenes and tumor suppressors in cancer cells.

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RESEARCH CHALLENGES IN STAGE III AND IV RAS-ASSOCIATED CANCERS: A Narrative Review of the Complexities and Functions of the Family of Genes and Ras Proteins in Housekeeping and Tumorigenesis.

Biology (Basel). 2025-7-25

[2]
Graphene Oxide-Functionalized Optical Sensor for Label-Free Detection of Breast Cancer Cells.

ACS Appl Nano Mater. 2025-8-18

[3]
Protein lipoylation in cancer: metabolic reprogramming and therapeutic potential.

Cell Death Discov. 2025-9-2

[4]
The osteosarcoma immune microenvironment in progression: PLEK as a prognostic biomarker and therapeutic target.

Front Immunol. 2025-8-15

[5]
Deciphering Medulloblastoma: Epigenetic and Metabolic Changes Driving Tumorigenesis and Treatment Outcomes.

Biomedicines. 2025-8-4

[6]
Targeting Lactylation: From Metabolic Reprogramming to Precision Therapeutics in Liver Diseases.

Biomolecules. 2025-8-16

[7]
Mitochondrial Metabolomics in Cancer: Mass Spectrometry-Based Approaches for Metabolic Rewiring Analysis and Therapeutic Discovery.

Metabolites. 2025-7-31

[8]
Diallyl Trisulfide Enhances Doxorubicin Chemosensitivity by Inhibiting the Warburg Effect and Inducing Apoptosis in Breast Cancer Cells.

J Cancer. 2025-7-11

[9]
Metabolic Reprogramming Shapes the Progression and Therapeutic Landscape of Ovarian Cancer.

Cancer Manag Res. 2025-8-19

[10]
Identification of malignant cells in single-cell transcriptomics data.

Commun Biol. 2025-8-22

本文引用的文献

[1]
The roles of histone modifications in tumorigenesis and associated inhibitors in cancer therapy.

J Natl Cancer Cent. 2022-9-28

[2]
Cancer incidence and mortality in China, 2022.

J Natl Cancer Cent. 2024-2-2

[3]
MCT1-dependent lactate recycling is a metabolic vulnerability in colorectal cancer cells upon acquired resistance to anti-EGFR targeted therapy.

Cancer Lett. 2024-8-28

[4]
Glutaminase - A potential target for cancer treatment.

Biomedicine (Taipei). 2024-6-1

[5]
Active DNA Demethylase, TET1, Increases Oxidative Phosphorylation and Sensitizes Ovarian Cancer Stem Cells to Mitochondrial Complex I Inhibitor.

Antioxidants (Basel). 2024-6-17

[6]
The PI3K/Akt Pathway and Glucose Metabolism: A Dangerous Liaison in Cancer.

Int J Biol Sci. 2024

[7]
Syrosingopine and UK5099 synergistically suppress non-small cell lung cancer by activating the integrated stress response.

Cell Death Dis. 2024-6-19

[8]
Hallmarks of cancer resistance.

iScience. 2024-5-15

[9]
GLUT1 promotes cell proliferation via binds and stabilizes phosphorylated EGFR in lung adenocarcinoma.

Cell Commun Signal. 2024-6-3

[10]
Tumor biomarkers for diagnosis, prognosis and targeted therapy.

Signal Transduct Target Ther. 2024-5-20

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