Amino Acid Metabolic Vulnerabilities in Acute and Chronic Myeloid Leukemias
Amino acid (AA) metabolism plays an important role in many cellular processes including energy production, immune function, and purine and pyrimidine synthesis. Cancer cells therefore require increased AA uptake and undergo metabolic reprogramming to satisfy the energy demand associated with their r...
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2021-07-01
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doaj-ff8a01113fdd4ca48c72b357f0870b542021-07-01T14:28:55ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-07-011110.3389/fonc.2021.694526694526Amino Acid Metabolic Vulnerabilities in Acute and Chronic Myeloid LeukemiasAboli Bhingarkar0Hima V. Vangapandu1Sanjay Rathod2Keito Hoshitsuki3Christian A. Fernandez4Center for Pharmacogenetics and Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, United StatesCenter for Pharmacogenetics and Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, United StatesCenter for Pharmacogenetics and Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, United StatesDivision of General Internal Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, United StatesCenter for Pharmacogenetics and Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, United StatesAmino acid (AA) metabolism plays an important role in many cellular processes including energy production, immune function, and purine and pyrimidine synthesis. Cancer cells therefore require increased AA uptake and undergo metabolic reprogramming to satisfy the energy demand associated with their rapid proliferation. Like many other cancers, myeloid leukemias are vulnerable to specific therapeutic strategies targeting metabolic dependencies. Herein, our review provides a comprehensive overview and TCGA data analysis of biosynthetic enzymes required for non-essential AA synthesis and their dysregulation in myeloid leukemias. Furthermore, we discuss the role of the general control nonderepressible 2 (GCN2) and-mammalian target of rapamycin (mTOR) pathways of AA sensing on metabolic vulnerability and drug resistance.https://www.frontiersin.org/articles/10.3389/fonc.2021.694526/fullnon-essential amino acidGCN2general control non-derepressible 2mTORC1myeloid leukemias |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Aboli Bhingarkar Hima V. Vangapandu Sanjay Rathod Keito Hoshitsuki Christian A. Fernandez |
spellingShingle |
Aboli Bhingarkar Hima V. Vangapandu Sanjay Rathod Keito Hoshitsuki Christian A. Fernandez Amino Acid Metabolic Vulnerabilities in Acute and Chronic Myeloid Leukemias Frontiers in Oncology non-essential amino acid GCN2 general control non-derepressible 2 mTORC1 myeloid leukemias |
author_facet |
Aboli Bhingarkar Hima V. Vangapandu Sanjay Rathod Keito Hoshitsuki Christian A. Fernandez |
author_sort |
Aboli Bhingarkar |
title |
Amino Acid Metabolic Vulnerabilities in Acute and Chronic Myeloid Leukemias |
title_short |
Amino Acid Metabolic Vulnerabilities in Acute and Chronic Myeloid Leukemias |
title_full |
Amino Acid Metabolic Vulnerabilities in Acute and Chronic Myeloid Leukemias |
title_fullStr |
Amino Acid Metabolic Vulnerabilities in Acute and Chronic Myeloid Leukemias |
title_full_unstemmed |
Amino Acid Metabolic Vulnerabilities in Acute and Chronic Myeloid Leukemias |
title_sort |
amino acid metabolic vulnerabilities in acute and chronic myeloid leukemias |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Oncology |
issn |
2234-943X |
publishDate |
2021-07-01 |
description |
Amino acid (AA) metabolism plays an important role in many cellular processes including energy production, immune function, and purine and pyrimidine synthesis. Cancer cells therefore require increased AA uptake and undergo metabolic reprogramming to satisfy the energy demand associated with their rapid proliferation. Like many other cancers, myeloid leukemias are vulnerable to specific therapeutic strategies targeting metabolic dependencies. Herein, our review provides a comprehensive overview and TCGA data analysis of biosynthetic enzymes required for non-essential AA synthesis and their dysregulation in myeloid leukemias. Furthermore, we discuss the role of the general control nonderepressible 2 (GCN2) and-mammalian target of rapamycin (mTOR) pathways of AA sensing on metabolic vulnerability and drug resistance. |
topic |
non-essential amino acid GCN2 general control non-derepressible 2 mTORC1 myeloid leukemias |
url |
https://www.frontiersin.org/articles/10.3389/fonc.2021.694526/full |
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