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The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells
- Source :
- PLoS ONE, PLoS ONE, Vol 12, Iss 5, p e0178174 (2017)
- Publication Year :
- 2017
-
Abstract
- The human protein ASPG is an enzyme with a putative antitumor activity. We generated in bacteria and then purified a recombinant GST-ASPG protein that we used to characterize the biochemical and cytotoxic properties of the human ASPG. We demonstrated that ASPG possesses asparaginase and PAF acetylhydrolase activities that depend on a critical threonine residue at position 19. Consistently, ASPG but not its T19A mutant showed cytotoxic activity in K562, NALM-6 and MOLT-4 leukemic cell lines but not in normal cells. Regarding the mechanism of action of ASPG, it was able to induce a significant apoptotic death in K562 cells. Taken together our data suggest that ASPG, combining different enzymatic activities, should be considered a promising anti-cancer agent for inhibiting the growth of leukemia cells.
- Subjects :
- 0301 basic medicine
PAF acetylhydrolase
Cytotoxicity
Cancer Treatment
lcsh:Medicine
Apoptosis
Toxicology
Pathology and Laboratory Medicine
Biochemistry
chemistry.chemical_compound
0302 clinical medicine
Medicine and Health Sciences
Cytotoxic T cell
Enzyme Inhibitors
lcsh:Science
chemistry.chemical_classification
Cultured Tumor Cells
Multidisciplinary
Leukemia
Cell Death
Recombinant Proteins
Enzymes
Chemistry
Oncology
Cell Processes
030220 oncology & carcinogenesis
Physical Sciences
Biological Cultures
medicine.symptom
Research Article
Asparaginase
Cell Survival
Recombinant Fusion Proteins
Antineoplastic Agents
Biology
Research and Analysis Methods
03 medical and health sciences
Ammonia
Cell Line, Tumor
medicine
Humans
Leukemia Cells
Epithelial Sodium Channels
Cell Proliferation
lcsh:R
Chemical Compounds
Biology and Life Sciences
Proteins
Cell Biology
Cell Cultures
Molecular biology
030104 developmental biology
Enzyme
chemistry
Mechanism of action
Amino Acid Substitution
Cell culture
1-Alkyl-2-acetylglycerophosphocholine Esterase
Mutagenesis, Site-Directed
Enzymology
lcsh:Q
K562 Cells
K562 cells
Subjects
Details
- ISSN :
- 19326203
- Volume :
- 12
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- PloS one
- Accession number :
- edsair.doi.dedup.....9f2288d8d1d44a1de97c7f5d02a84ec6