1-C Metabolism—Serine, Glycine, Folates—In Acute Myeloid Leukemia

Metabolic reprogramming contributes to tumor development and introduces metabolic liabilities that can be exploited to treat cancer. Studies in hematological malignancies have shown alterations in fatty acid, folate, and amino acid metabolism pathways in cancer cells. One-carbon (1-C) metabolism is...

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Main Authors: Kanwal Mahmood, Ashkan Emadi
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/14/3/190
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author Kanwal Mahmood
Ashkan Emadi
author_facet Kanwal Mahmood
Ashkan Emadi
author_sort Kanwal Mahmood
collection DOAJ
description Metabolic reprogramming contributes to tumor development and introduces metabolic liabilities that can be exploited to treat cancer. Studies in hematological malignancies have shown alterations in fatty acid, folate, and amino acid metabolism pathways in cancer cells. One-carbon (1-C) metabolism is essential for numerous cancer cell functions, including protein and nucleic acid synthesis and maintaining cellular redox balance, and inhibition of the 1-C pathway has yielded several highly active drugs, such as methotrexate and 5-FU. Glutamine depletion has also emerged as a therapeutic approach for cancers that have demonstrated dependence on glutamine for survival. Recent studies have shown that in response to glutamine deprivation leukemia cells upregulate key enzymes in the serine biosynthesis pathway, suggesting that serine upregulation may be a targetable compensatory mechanism. These new findings may provide opportunities for novel cancer treatments.
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spelling doaj.art-0f49afc8ba184d2eb7aec978fcbec9182023-12-11T18:32:31ZengMDPI AGPharmaceuticals1424-82472021-02-0114319010.3390/ph140301901-C Metabolism—Serine, Glycine, Folates—In Acute Myeloid LeukemiaKanwal Mahmood0Ashkan Emadi1Department of Medicine, School of Medicine, University of Maryland, Baltimore, MD 21201, USADepartment of Medicine, School of Medicine, University of Maryland, Baltimore, MD 21201, USAMetabolic reprogramming contributes to tumor development and introduces metabolic liabilities that can be exploited to treat cancer. Studies in hematological malignancies have shown alterations in fatty acid, folate, and amino acid metabolism pathways in cancer cells. One-carbon (1-C) metabolism is essential for numerous cancer cell functions, including protein and nucleic acid synthesis and maintaining cellular redox balance, and inhibition of the 1-C pathway has yielded several highly active drugs, such as methotrexate and 5-FU. Glutamine depletion has also emerged as a therapeutic approach for cancers that have demonstrated dependence on glutamine for survival. Recent studies have shown that in response to glutamine deprivation leukemia cells upregulate key enzymes in the serine biosynthesis pathway, suggesting that serine upregulation may be a targetable compensatory mechanism. These new findings may provide opportunities for novel cancer treatments.https://www.mdpi.com/1424-8247/14/3/190amino acid metabolismcancer therapyleukemiaamino-acid-degrading enzymesamino acid restriction in cancer
spellingShingle Kanwal Mahmood
Ashkan Emadi
1-C Metabolism—Serine, Glycine, Folates—In Acute Myeloid Leukemia
Pharmaceuticals
amino acid metabolism
cancer therapy
leukemia
amino-acid-degrading enzymes
amino acid restriction in cancer
title 1-C Metabolism—Serine, Glycine, Folates—In Acute Myeloid Leukemia
title_full 1-C Metabolism—Serine, Glycine, Folates—In Acute Myeloid Leukemia
title_fullStr 1-C Metabolism—Serine, Glycine, Folates—In Acute Myeloid Leukemia
title_full_unstemmed 1-C Metabolism—Serine, Glycine, Folates—In Acute Myeloid Leukemia
title_short 1-C Metabolism—Serine, Glycine, Folates—In Acute Myeloid Leukemia
title_sort 1 c metabolism serine glycine folates in acute myeloid leukemia
topic amino acid metabolism
cancer therapy
leukemia
amino-acid-degrading enzymes
amino acid restriction in cancer
url https://www.mdpi.com/1424-8247/14/3/190
work_keys_str_mv AT kanwalmahmood 1cmetabolismserineglycinefolatesinacutemyeloidleukemia
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