Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer

Integrins are important regulators of cell survival, proliferation, adhesion and migration. Once activated, integrins establish a regulated link between the extracellular matrix and the cytoskeleton. Integrins have well-established functions in cancer, such as in controlling cell survival by engagem...

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Main Authors: Rehman Ata, Costin N. Antonescu
Format: Article
Language:English
Published: MDPI AG 2017-01-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/18/1/189
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spelling doaj-99ffa79632ad4be1b1f82d4ee553db3f2020-11-24T20:43:47ZengMDPI AGInternational Journal of Molecular Sciences1422-00672017-01-0118118910.3390/ijms18010189ijms18010189Integrins and Cell Metabolism: An Intimate Relationship Impacting CancerRehman Ata0Costin N. Antonescu1Department of Chemistry and Biology, Ryerson University, 350 Victoria Street, Toronto, ON M5B 2K3, CanadaDepartment of Chemistry and Biology, Ryerson University, 350 Victoria Street, Toronto, ON M5B 2K3, CanadaIntegrins are important regulators of cell survival, proliferation, adhesion and migration. Once activated, integrins establish a regulated link between the extracellular matrix and the cytoskeleton. Integrins have well-established functions in cancer, such as in controlling cell survival by engagement of many specific intracellular signaling pathways and in facilitating metastasis. Integrins and associated proteins are regulated by control of transcription, membrane traffic, and degradation, as well as by a number of post-translational modifications including glycosylation, allowing integrin function to be modulated to conform to various cellular needs and environmental conditions. In this review, we examine the control of integrin function by cell metabolism, and the impact of this regulation in cancer. Within this context, nutrient sufficiency or deprivation is sensed by a number of metabolic signaling pathways such as AMP-activated protein kinase (AMPK), mammalian target of rapamycin (mTOR) and hypoxia-inducible factor (HIF) 1, which collectively control integrin function by a number of mechanisms. Moreover, metabolic flux through specific pathways also controls integrins, such as by control of integrin glycosylation, thus impacting integrin-dependent cell adhesion and migration. Integrins also control various metabolic signals and pathways, establishing the reciprocity of this regulation. As cancer cells exhibit substantial changes in metabolism, such as a shift to aerobic glycolysis, enhanced glucose utilization and a heightened dependence on specific amino acids, the reciprocal regulation of integrins and metabolism may provide important clues for more effective treatment of various cancers.http://www.mdpi.com/1422-0067/18/1/189AMPKmTORHIF1membrane trafficglycosylationhypoxianutrient deficitcancer metabolismmetabolic stress
collection DOAJ
language English
format Article
sources DOAJ
author Rehman Ata
Costin N. Antonescu
spellingShingle Rehman Ata
Costin N. Antonescu
Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer
International Journal of Molecular Sciences
AMPK
mTOR
HIF1
membrane traffic
glycosylation
hypoxia
nutrient deficit
cancer metabolism
metabolic stress
author_facet Rehman Ata
Costin N. Antonescu
author_sort Rehman Ata
title Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer
title_short Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer
title_full Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer
title_fullStr Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer
title_full_unstemmed Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer
title_sort integrins and cell metabolism: an intimate relationship impacting cancer
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2017-01-01
description Integrins are important regulators of cell survival, proliferation, adhesion and migration. Once activated, integrins establish a regulated link between the extracellular matrix and the cytoskeleton. Integrins have well-established functions in cancer, such as in controlling cell survival by engagement of many specific intracellular signaling pathways and in facilitating metastasis. Integrins and associated proteins are regulated by control of transcription, membrane traffic, and degradation, as well as by a number of post-translational modifications including glycosylation, allowing integrin function to be modulated to conform to various cellular needs and environmental conditions. In this review, we examine the control of integrin function by cell metabolism, and the impact of this regulation in cancer. Within this context, nutrient sufficiency or deprivation is sensed by a number of metabolic signaling pathways such as AMP-activated protein kinase (AMPK), mammalian target of rapamycin (mTOR) and hypoxia-inducible factor (HIF) 1, which collectively control integrin function by a number of mechanisms. Moreover, metabolic flux through specific pathways also controls integrins, such as by control of integrin glycosylation, thus impacting integrin-dependent cell adhesion and migration. Integrins also control various metabolic signals and pathways, establishing the reciprocity of this regulation. As cancer cells exhibit substantial changes in metabolism, such as a shift to aerobic glycolysis, enhanced glucose utilization and a heightened dependence on specific amino acids, the reciprocal regulation of integrins and metabolism may provide important clues for more effective treatment of various cancers.
topic AMPK
mTOR
HIF1
membrane traffic
glycosylation
hypoxia
nutrient deficit
cancer metabolism
metabolic stress
url http://www.mdpi.com/1422-0067/18/1/189
work_keys_str_mv AT rehmanata integrinsandcellmetabolismanintimaterelationshipimpactingcancer
AT costinnantonescu integrinsandcellmetabolismanintimaterelationshipimpactingcancer
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