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The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells

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 acetylhy...

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Autores principales: Belviso, Stefania, Iuliano, Rodolfo, Amato, Rosario, Perrotti, Nicola, Menniti, Miranda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443537/
https://www.ncbi.nlm.nih.gov/pubmed/28542249
http://dx.doi.org/10.1371/journal.pone.0178174
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author Belviso, Stefania
Iuliano, Rodolfo
Amato, Rosario
Perrotti, Nicola
Menniti, Miranda
author_facet Belviso, Stefania
Iuliano, Rodolfo
Amato, Rosario
Perrotti, Nicola
Menniti, Miranda
author_sort Belviso, Stefania
collection PubMed
description 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.
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spelling pubmed-54435372017-06-06 The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells Belviso, Stefania Iuliano, Rodolfo Amato, Rosario Perrotti, Nicola Menniti, Miranda PLoS One Research Article 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. Public Library of Science 2017-05-24 /pmc/articles/PMC5443537/ /pubmed/28542249 http://dx.doi.org/10.1371/journal.pone.0178174 Text en © 2017 Belviso et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Belviso, Stefania
Iuliano, Rodolfo
Amato, Rosario
Perrotti, Nicola
Menniti, Miranda
The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells
title The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells
title_full The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells
title_fullStr The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells
title_full_unstemmed The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells
title_short The human asparaginase enzyme (ASPG) inhibits growth in leukemic cells
title_sort human asparaginase enzyme (aspg) inhibits growth in leukemic cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443537/
https://www.ncbi.nlm.nih.gov/pubmed/28542249
http://dx.doi.org/10.1371/journal.pone.0178174
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