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lncRNAs: Key Regulators of Signaling Pathways in Tumor Glycolysis

In response to overstimulation of growth factor signaling, tumor cells can reprogram their metabolism to preferentially utilize and metabolize glucose to lactate even in the presence of abundant oxygen, which is termed the “Warburg effect” or aerobic glycolysis. Long noncoding RNAs (lncRNAs) are a g...

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Detalles Bibliográficos
Autores principales: Wen, Li, Tan, Chang, Ma, Shuai, Li, Xinzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482549/
https://www.ncbi.nlm.nih.gov/pubmed/36124026
http://dx.doi.org/10.1155/2022/2267963
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author Wen, Li
Tan, Chang
Ma, Shuai
Li, Xinzhi
author_facet Wen, Li
Tan, Chang
Ma, Shuai
Li, Xinzhi
author_sort Wen, Li
collection PubMed
description In response to overstimulation of growth factor signaling, tumor cells can reprogram their metabolism to preferentially utilize and metabolize glucose to lactate even in the presence of abundant oxygen, which is termed the “Warburg effect” or aerobic glycolysis. Long noncoding RNAs (lncRNAs) are a group of transcripts longer than 200 nucleotides and do not encode proteins. Accumulating evidence suggests that lncRNAs can affect aerobic glycolysis through multiple mechanisms, including the regulation of glycolytic transporters and key rate-limiting enzymes. In addition, maladjusted signaling pathways are critical for glycolysis. Therefore, this article mainly reviews the lncRNAs involved in the regulation of tumor glycolysis key signal pathways in recent years and provides an in-depth understanding of the role of differentially expressed lncRNAs in the key signal pathways of glucose metabolism, which may help to provide new therapeutic targets and new diagnostic and prognostic markers for human cancer.
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spelling pubmed-94825492022-09-18 lncRNAs: Key Regulators of Signaling Pathways in Tumor Glycolysis Wen, Li Tan, Chang Ma, Shuai Li, Xinzhi Dis Markers Review Article In response to overstimulation of growth factor signaling, tumor cells can reprogram their metabolism to preferentially utilize and metabolize glucose to lactate even in the presence of abundant oxygen, which is termed the “Warburg effect” or aerobic glycolysis. Long noncoding RNAs (lncRNAs) are a group of transcripts longer than 200 nucleotides and do not encode proteins. Accumulating evidence suggests that lncRNAs can affect aerobic glycolysis through multiple mechanisms, including the regulation of glycolytic transporters and key rate-limiting enzymes. In addition, maladjusted signaling pathways are critical for glycolysis. Therefore, this article mainly reviews the lncRNAs involved in the regulation of tumor glycolysis key signal pathways in recent years and provides an in-depth understanding of the role of differentially expressed lncRNAs in the key signal pathways of glucose metabolism, which may help to provide new therapeutic targets and new diagnostic and prognostic markers for human cancer. Hindawi 2022-09-10 /pmc/articles/PMC9482549/ /pubmed/36124026 http://dx.doi.org/10.1155/2022/2267963 Text en Copyright © 2022 Li Wen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Wen, Li
Tan, Chang
Ma, Shuai
Li, Xinzhi
lncRNAs: Key Regulators of Signaling Pathways in Tumor Glycolysis
title lncRNAs: Key Regulators of Signaling Pathways in Tumor Glycolysis
title_full lncRNAs: Key Regulators of Signaling Pathways in Tumor Glycolysis
title_fullStr lncRNAs: Key Regulators of Signaling Pathways in Tumor Glycolysis
title_full_unstemmed lncRNAs: Key Regulators of Signaling Pathways in Tumor Glycolysis
title_short lncRNAs: Key Regulators of Signaling Pathways in Tumor Glycolysis
title_sort lncrnas: key regulators of signaling pathways in tumor glycolysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482549/
https://www.ncbi.nlm.nih.gov/pubmed/36124026
http://dx.doi.org/10.1155/2022/2267963
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