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Targeting Asparagine Metabolism in Solid Tumors.

作者信息

Hanada Keita, Kawada Kenji, Obama Kazutaka

机构信息

Department of Gastrointestinal Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Department of Surgery, Rakuwakai Otowa Hospital, Kyoto 607-8062, Japan.

出版信息

Nutrients. 2025 Jan 3;17(1):179. doi: 10.3390/nu17010179.


DOI:10.3390/nu17010179
PMID:39796613
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11722615/
Abstract

Reprogramming of energy metabolism to support cellular growth is a "hallmark" of cancer, allowing cancer cells to balance the catabolic demands with the anabolic needs of producing the nucleotides, amino acids, and lipids necessary for tumor growth. Metabolic alterations, or "addiction", are promising therapeutic targets and the focus of many drug discovery programs. Asparagine metabolism has gained much attention in recent years as a novel target for cancer therapy. Asparagine is widely used in the production of other nutrients and plays an important role in cancer development. Nutritional inhibition therapy targeting asparagine has been used as an anticancer strategy and has shown success in the treatment of leukemia. However, in solid tumors, asparagine restriction alone does not provide ideal therapeutic efficacy. Tumor cells initiate reprogramming processes in response to asparagine deprivation. This review provides a comprehensive overview of asparagine metabolism in cancers. We highlight the physiological role of asparagine and current advances in improving survival and overcoming therapeutic resistance.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3092/11722615/342b612aada8/nutrients-17-00179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3092/11722615/10eecdcc5592/nutrients-17-00179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3092/11722615/342b612aada8/nutrients-17-00179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3092/11722615/10eecdcc5592/nutrients-17-00179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3092/11722615/342b612aada8/nutrients-17-00179-g002.jpg

相似文献

[1]
Targeting Asparagine Metabolism in Solid Tumors.

Nutrients. 2025-1-3

[2]
Asparagine: A key metabolic junction in targeted tumor therapy.

Pharmacol Res. 2024-8

[3]
Metabolism of asparagine in the physiological state and cancer.

Cell Commun Signal. 2024-3-6

[4]
Targeting amino acid metabolism in cancer.

Int Rev Cell Mol Biol. 2022

[5]
Exploring the potential of asparagine restriction in solid cancer treatment: recent discoveries, therapeutic implications, and challenges.

Med Oncol. 2024-6-15

[6]
Drug discovery strategies in the field of tumor energy metabolism: Limitations by metabolic flexibility and metabolic resistance to chemotherapy.

Biochim Biophys Acta Bioenerg. 2017-2-16

[7]
Targeting KRAS: from metabolic regulation to cancer treatment.

Mol Cancer. 2025-1-11

[8]
Glycogen metabolism has a key role in the cancer microenvironment and provides new targets for cancer therapy.

J Mol Med (Berl). 2016-2

[9]
A Critical Role of Glutamine and Asparagine γ-Nitrogen in Nucleotide Biosynthesis in Cancer Cells Hijacked by an Oncogenic Virus.

mBio. 2017-8-15

[10]
Targeting Asparagine Synthetase in Tumorgenicity Using Patient-Derived Tumor-Initiating Cells.

Cells. 2022-10-18

本文引用的文献

[1]
Identifying targetable metabolic dependencies across colorectal cancer progression.

Mol Metab. 2024-12

[2]
Asparagine Dependency Is a Targetable Metabolic Vulnerability in TP53-Altered Castration-Resistant Prostate Cancer.

Cancer Res. 2024-9-16

[3]
Growth characteristics of HCT116 xenografts lacking asparagine synthetase vary according to sex.

Hum Genomics. 2024-6-17

[4]
AURKA emerges as a vulnerable target for KEAP1-deficient non-small cell lung cancer by activation of asparagine synthesis.

Cell Death Dis. 2024-3-23

[5]
Metabolism of asparagine in the physiological state and cancer.

Cell Commun Signal. 2024-3-6

[6]
Transmembrane protein 176B regulates amino acid metabolism through the PI3K-Akt-mTOR signaling pathway and promotes gastric cancer progression.

Cancer Cell Int. 2024-3-4

[7]
Bisabosqual A: A novel asparagine synthetase inhibitor suppressing the proliferation and migration of human non-small cell lung cancer A549 cells.

Eur J Pharmacol. 2023-12-5

[8]
Arginine reprograms metabolism in liver cancer via RBM39.

Cell. 2023-11-9

[9]
Targeting TLK2 inhibits the progression of gastric cancer by reprogramming amino acid metabolism through the mTOR/ASNS axis.

Cancer Gene Ther. 2023-11

[10]
NUCKS1, a LINC00629-upregulated gene, facilitated osteosarcoma progression and metastasis by elevating asparagine synthesis.

Cell Death Dis. 2023-8-1

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