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The Effect of a New Glucose-Methotrexate Conjugate on Acute Lymphoblastic Leukemia and Non-Hodgkin's Lymphoma Cell Lines

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2021 Apr 30
PMID 33925555
Citations 2
Authors
Affiliations
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Abstract

Patients with hematologic malignancies require intensive therapies, including high-dose chemotherapy. Antimetabolite-methotrexate (MTX) has been used for many years in the treatment of leukemia and in lymphoma patients. However, the lack of MTX specificity causes a significant risk of morbidity, mortality, and severe side effects that impairs the quality of patients' life. Therefore, novel targeted therapies based on the malignant cells' common traits have become an essential treatment strategy. Glucose transporters have been found to be overexpressed in neoplastic cells, including hematologic malignancies. In this study, we biologically evaluated a novel glucose-methotrexate conjugate (Glu-MTX) in comparison to a free MTX. The research aimed to assess the effectiveness of Glu-MTX on chosen human lymphoma and leukemia cell lines. Cell cytotoxicity was verified by MTT viability test and flow cytometry. Moreover, the cell cycle and cellular uptake of Glu-MTX were evaluated. Our study reveals that conjugation of methotrexate with glucose significantly increases drug uptake and results in similar cytotoxicity of the synthesized compound. Although the finding has been confined to in vitro studies, our observations shed light on a potential therapeutic approach that increases the selectivity of chemotherapeutics and can improve leukemia and lymphoma patients' outcomes.

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References
1.
Barbosa A, Martel F . Targeting Glucose Transporters for Breast Cancer Therapy: The Effect of Natural and Synthetic Compounds. Cancers (Basel). 2020; 12(1). PMC: 7016663. DOI: 10.3390/cancers12010154. View

2.
Li H, Gao X, Liu R, Wang Y, Zhang M, Fu Z . Glucose conjugated platinum(II) complex: antitumor superiority to oxaliplatin, combination effect and mechanism of action. Eur J Med Chem. 2015; 101:400-8. DOI: 10.1016/j.ejmech.2015.07.006. View

3.
Simon F, Garcia Borrega J, Brockelmann P . Toxicities of novel therapies for hematologic malignancies. Expert Rev Hematol. 2020; 13(3):241-257. DOI: 10.1080/17474086.2020.1728249. View

4.
Klener Jr P, Etrych T, Klener P . Biological Therapy of Hematologic Malignancies: Toward a Chemotherapy- free Era. Curr Med Chem. 2017; 26(6):1002-1018. DOI: 10.2174/0929867324666171006144725. View

5.
Thirumurugan P, Matosiuk D, Jozwiak K . Click chemistry for drug development and diverse chemical-biology applications. Chem Rev. 2013; 113(7):4905-79. DOI: 10.1021/cr200409f. View