Role of Metabolic Reprogramming in Epithelial–Mesenchymal Transition (EMT)
Роль метаболического перепрограммирования в эпителиально-мезенхимальном переходе (ЭМП)
2019-04-25
SCID: 54.1/jmarx82w
Discuss with AI
cancer metastasisepithelial–mesenchymal transitionmetabolic enzyme inhibitionmetabolic reprogrammingtumor metabolism
Figures from the paper
Abstract (AI)
Activation of epithelial-mesenchymal transition (EMT) is thought to be an essential step for cancer metastasis. Tumor cells undergo EMT in response to a diverse range of extra- and intracellular stimulants. Recently, it was reported that metabolic shifts control EMT progression and induce tumor aggressiveness. In this review, we summarize the involvement of altered glucose, lipid, and amino acid metabolic enzyme expression and the underlying molecular mechanisms in EMT induction in tumor cells. Moreover, we propose that metabolic regulation through gene-specific or pharmacological inhibition may suppress EMT and this treatment strategy may be applied to prevent tumor progression and improve anti-tumor therapeutic efficacy. This review presents evidence for the importance of metabolic changes in tumor progression and emphasizes the need for further studies to better understand tumor metabolism.
Key Findings
1
Altered expression of glucose, lipid, and amino acid metabolic enzymes contributes to EMT induction through underlying molecular mechanisms.
2
Gene-specific or pharmacological inhibition of metabolic regulation may suppress EMT and help prevent tumor progression.
3
Metabolic shifts are reported to control epithelial–mesenchymal transition (EMT) progression and promote tumor aggressiveness.
4
Targeting tumor metabolism could improve the efficacy of anticancer therapies, although further studies are needed to clarify these mechanisms.
Research Object
tumor cells undergoing epithelial–mesenchymal transition (EMT)
Research Subject
the role and molecular mechanisms of altered glucose, lipid, and amino acid metabolism in EMT induction and tumor aggressiveness
Publication Details
Publication Date
2019-04-25
Journal
Publisher
ISSN
Open access PDF
Access Type
Author Information
Download PDF
Subscribe to digest