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耐药癌细胞中葡萄糖依赖性改变的图示。

The Illustration of Altered Glucose Dependency in Drug-Resistant Cancer Cells.

机构信息

Department of Anatomy, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.

出版信息

Int J Mol Sci. 2023 Sep 11;24(18):13928. doi: 10.3390/ijms241813928.


DOI:10.3390/ijms241813928
PMID:37762231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10530558/
Abstract

A chemotherapeutic approach is crucial in malignancy management, which is often challenging due to the development of chemoresistance. Over time, chemo-resistant cancer cells rapidly repopulate and metastasize, increasing the recurrence rate in cancer patients. Targeting these destined cancer cells is more troublesome for clinicians, as they share biology and molecular cross-talks with normal cells. However, the recent insights into the metabolic profiles of chemo-resistant cancer cells surprisingly illustrated the activation of distinct pathways compared with chemo-sensitive or primary cancer cells. These distinct metabolic dynamics are vital and contribute to the shift from chemo-sensitivity to chemo-resistance in cancer. This review will discuss the important metabolic alterations in cancer cells that lead to drug resistance.

摘要

化疗方法在恶性肿瘤的治疗中至关重要,但由于化疗耐药性的发展,这往往具有挑战性。随着时间的推移,化疗耐药的癌细胞迅速增殖并转移,增加了癌症患者的复发率。对临床医生来说,靶向这些注定的癌细胞更加麻烦,因为它们与正常细胞具有相似的生物学和分子串扰。然而,最近对化疗耐药癌细胞代谢特征的深入研究表明,与化疗敏感或原发性癌细胞相比,这些细胞中存在明显激活的不同途径。这些不同的代谢动态是至关重要的,它们导致了癌细胞从化疗敏感性向化疗耐药性的转变。本综述将讨论导致药物耐药性的癌细胞中重要的代谢改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/27a0018fcf3e/ijms-24-13928-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/5e9b463a52bc/ijms-24-13928-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/3c27fcbceb65/ijms-24-13928-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/b6ce996ce2d8/ijms-24-13928-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/819ada938f7a/ijms-24-13928-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/9f4f30aa30ce/ijms-24-13928-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/27a0018fcf3e/ijms-24-13928-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/5e9b463a52bc/ijms-24-13928-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/3c27fcbceb65/ijms-24-13928-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/b6ce996ce2d8/ijms-24-13928-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/819ada938f7a/ijms-24-13928-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/9f4f30aa30ce/ijms-24-13928-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/27a0018fcf3e/ijms-24-13928-g006.jpg

相似文献

[1]
The Illustration of Altered Glucose Dependency in Drug-Resistant Cancer Cells.

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[2]
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[6]
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[7]
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[8]
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[10]
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引用本文的文献

[1]
Exploring glycolytic enzymes in disease: potential biomarkers and therapeutic targets in neurodegeneration, cancer and parasitic infections.

Open Biol. 2025-2

[2]
Inhibition of FBP1 expression by KMT5A through TWIST1 methylation is one of the mechanisms leading to chemoresistance in breast cancer.

Oncol Rep. 2024-8

本文引用的文献

[1]
Participation of protein metabolism in cancer progression and its potential targeting for the management of cancer.

Amino Acids. 2023-10

[2]
The regulation of amino acid metabolism in tumor cell death: from the perspective of physiological functions.

Apoptosis. 2023-10

[3]
The metabolic function of pyruvate kinase M2 regulates reactive oxygen species production and microbial killing by neutrophils.

Nat Commun. 2023-7-17

[4]
Cancer chemotherapy and beyond: Current status, drug candidates, associated risks and progress in targeted therapeutics.

Genes Dis. 2022-3-18

[5]
Metformin and cancer hallmarks: shedding new lights on therapeutic repurposing.

J Transl Med. 2023-6-21

[6]
Signaling pathways in cancer metabolism: mechanisms and therapeutic targets.

Signal Transduct Target Ther. 2023-5-10

[7]
Metabolic reprogramming in cancer: Mechanisms and therapeutics.

MedComm (2020). 2023-3-27

[8]
How Warburg-Associated Lactic Acidosis Rewires Cancer Cell Energy Metabolism to Resist Glucose Deprivation.

Cancers (Basel). 2023-2-23

[9]
Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics.

Front Immunol. 2022-12-22

[10]
Inhibition of TIGAR Increases Exogenous p53 and Cisplatin Combination Sensitivity in Lung Cancer Cells by Regulating Glycolytic Flux.

Int J Mol Sci. 2022-12-16

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