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On the cytotoxicity of HCR-NTPase in the neuroblastoma cell line SH-SY5Y
BACKGROUND: The human cancer-related nucleoside triphosphatase (HCR-NTPase) is overexpressed in several tumour tissues including neuroblastoma. HCR-NTPase is an enzyme exhibiting a slow in vitro activity in hydrolysing nucleosidetriphosphates. However, its in vivo function is still unknown. To learn...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700126/ https://www.ncbi.nlm.nih.gov/pubmed/19519914 http://dx.doi.org/10.1186/1756-0500-2-102 |
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author | Pasdziernik, Markus Kaltschmidt, Barbara Kaltschmidt, Christian Klinger, Claudia Kaufmann, Michael |
author_facet | Pasdziernik, Markus Kaltschmidt, Barbara Kaltschmidt, Christian Klinger, Claudia Kaufmann, Michael |
author_sort | Pasdziernik, Markus |
collection | PubMed |
description | BACKGROUND: The human cancer-related nucleoside triphosphatase (HCR-NTPase) is overexpressed in several tumour tissues including neuroblastoma. HCR-NTPase is an enzyme exhibiting a slow in vitro activity in hydrolysing nucleosidetriphosphates. However, its in vivo function is still unknown. To learn more about the physiological role of HCR-NTPase, we both overexpressed and silenced it in the neuroblastoma cell line SH-SY5Y. FINDINGS: No effect was observed when the expression of endogenously expressed HCR-NTPase in the cells was silenced by RNA interference. On the other hand, overexpression of HCR-NTPase led to cytotoxicity of the protein in SH-SY5Y cells. Even if the catalytic essential amino acid glutamate 114 was replaced by alanine (E114A-HCR-NTPase), the protein remained cytotoxic. The results could be confirmed by successfully rescuing the cells via RNA interference. CONCLUSION: Although expressed in several tumours, at least in SH-SY5Y, HCR-NTPase is not essential for the cells to survive. Increased levels of the protein lead to cytotoxicity due to physical intracellular interactions rather than hydrolysis of nucleosidetriphosphates by its intrinsic residual enzymatic activity. |
format | Text |
id | pubmed-2700126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27001262009-06-23 On the cytotoxicity of HCR-NTPase in the neuroblastoma cell line SH-SY5Y Pasdziernik, Markus Kaltschmidt, Barbara Kaltschmidt, Christian Klinger, Claudia Kaufmann, Michael BMC Res Notes Short Report BACKGROUND: The human cancer-related nucleoside triphosphatase (HCR-NTPase) is overexpressed in several tumour tissues including neuroblastoma. HCR-NTPase is an enzyme exhibiting a slow in vitro activity in hydrolysing nucleosidetriphosphates. However, its in vivo function is still unknown. To learn more about the physiological role of HCR-NTPase, we both overexpressed and silenced it in the neuroblastoma cell line SH-SY5Y. FINDINGS: No effect was observed when the expression of endogenously expressed HCR-NTPase in the cells was silenced by RNA interference. On the other hand, overexpression of HCR-NTPase led to cytotoxicity of the protein in SH-SY5Y cells. Even if the catalytic essential amino acid glutamate 114 was replaced by alanine (E114A-HCR-NTPase), the protein remained cytotoxic. The results could be confirmed by successfully rescuing the cells via RNA interference. CONCLUSION: Although expressed in several tumours, at least in SH-SY5Y, HCR-NTPase is not essential for the cells to survive. Increased levels of the protein lead to cytotoxicity due to physical intracellular interactions rather than hydrolysis of nucleosidetriphosphates by its intrinsic residual enzymatic activity. BioMed Central 2009-06-11 /pmc/articles/PMC2700126/ /pubmed/19519914 http://dx.doi.org/10.1186/1756-0500-2-102 Text en Copyright © 2009 Kaufmann et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Pasdziernik, Markus Kaltschmidt, Barbara Kaltschmidt, Christian Klinger, Claudia Kaufmann, Michael On the cytotoxicity of HCR-NTPase in the neuroblastoma cell line SH-SY5Y |
title | On the cytotoxicity of HCR-NTPase in the neuroblastoma cell line SH-SY5Y |
title_full | On the cytotoxicity of HCR-NTPase in the neuroblastoma cell line SH-SY5Y |
title_fullStr | On the cytotoxicity of HCR-NTPase in the neuroblastoma cell line SH-SY5Y |
title_full_unstemmed | On the cytotoxicity of HCR-NTPase in the neuroblastoma cell line SH-SY5Y |
title_short | On the cytotoxicity of HCR-NTPase in the neuroblastoma cell line SH-SY5Y |
title_sort | on the cytotoxicity of hcr-ntpase in the neuroblastoma cell line sh-sy5y |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700126/ https://www.ncbi.nlm.nih.gov/pubmed/19519914 http://dx.doi.org/10.1186/1756-0500-2-102 |
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