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Restored biosynthetic pathways induced by MSCs serve as rescue mechanism in leukemia cells after L-asparaginase therapy
- 1.0574564 - FGÚ 2024 RIV NL eng J - Článek v odborném periodiku
Alquezar-Artieda, N. - Kužílková, D. - Roberts, J. - Hložková, K. - Pecinová, Alena - Pecina, Petr - Zwyrtková, M. - Potůčková, E. - Kavan, Daniel - Heřmanová, I. - Žaliová, M. - Novák, Petr - Mráček, Tomáš - Šrámková, L. - Tennant, D. A. - Trka, J. - Starková, J.
Restored biosynthetic pathways induced by MSCs serve as rescue mechanism in leukemia cells after L-asparaginase therapy.
Blood Advances. Roč. 7, č. 10 (2023), s. 2228-2236. ISSN 2473-9529. E-ISSN 2473-9537
Grant CEP: GA ČR(CZ) GA21-18993S; GA MŠMT LX22NPO5102
Institucionální podpora: RVO:67985823 ; RVO:61388971
Klíčová slova: cancer metabolism * L-asparaginase * leukemia * resistance * glycolysis * fatty acid oxidation * MSCs * biosynthetic pathways
Obor OECD: Endocrinology and metabolism (including diabetes, hormones); Biochemistry and molecular biology (MBU-M)
Impakt faktor: 7.6, rok: 2022
Způsob publikování: Open access
https://doi.org/10.1182/bloodadvances.2021006431
L-asparaginase (ASNase), the drug included on the World Health Organization’s list of essential medicines, is irreplaceable in the front-line treatment of childhood acute lymphoblastic leukemia (ALL). However, the relapse of ALL is often associated with resistance to ASNase and its mechanisms are not fully understood. The cytotoxic effect of ASNase relies on depleting exogenous asparagine (Asn) and glutamine (Gln), inducing apoptosis in leukemic cells because of their reduced capability of Asn synthesis. Our previous in vitro data demonstrated that ASNase triggers metabolic reprogramming of leukemic cells, which impedes the anti-leukemic effect. Metabolic processes of leukemic cells have been shown to be altered by the environment of the bone marrow (BM), which may contribute to chemoresistance. Herein, we investigated the impact of BM attributes on cellular metabolic processes of leukemic cells in order to demonstrate the more complex picture of ASNase-driven metabolic rewiring and its role in the mechanism of resistance.
Trvalý link: https://hdl.handle.net/11104/0345499
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