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Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia – preliminary report

AIM OF THE STUDY: To characterise expression of mTOR (mammalian target of rapamycin) in childhood B-cell acute lymphoblastic leukaemia (ALL), and to evaluate a possible link between mTOR and clinical characteristics. MATERIAL AND METHODS: The examined group consisted of 21 consecutive patients, aged...

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Autores principales: Ulińska, Edyta, Mycko, Katarzyna, Sałacińska-Łoś, Elżbieta, Pastorczak, Agata, Siwicka, Alicja, Młynarski, Wojciech, Matysiak, Michał
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5032156/
https://www.ncbi.nlm.nih.gov/pubmed/27688725
http://dx.doi.org/10.5114/wo.2016.61848
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author Ulińska, Edyta
Mycko, Katarzyna
Sałacińska-Łoś, Elżbieta
Pastorczak, Agata
Siwicka, Alicja
Młynarski, Wojciech
Matysiak, Michał
author_facet Ulińska, Edyta
Mycko, Katarzyna
Sałacińska-Łoś, Elżbieta
Pastorczak, Agata
Siwicka, Alicja
Młynarski, Wojciech
Matysiak, Michał
author_sort Ulińska, Edyta
collection PubMed
description AIM OF THE STUDY: To characterise expression of mTOR (mammalian target of rapamycin) in childhood B-cell acute lymphoblastic leukaemia (ALL), and to evaluate a possible link between mTOR and clinical characteristics. MATERIAL AND METHODS: The examined group consisted of 21 consecutive patients, aged 1–18 years, diagnosed with B-cell ALL in 2010, and 10 relapsed B-cell ALL patients diagnosed for the first time between 2009 and 2011, who developed relapse before 2014. All subjects were treated in the Department of Paediatric Haematology and Oncology of the Medical University of Warsaw according to the ALL-IC BFM 2002 Protocol. We evaluated mTOR and phospho-mTOR expression by immunohistochemistry using rabbit monoclonal antibodies. RESULTS: mTOR expression was found to be significantly associated with the risk of relapse and was more frequent in ALL recurrence. No significant relationship was detected between mTOR expression and other features of high-risk disease in paediatric ALL. CONCLUSIONS: mTOR activity could be considered a high-risk feature in paediatric B-cell ALL. Expression of mTOR kinase is observed remarkably more frequently in disease recurrence than at first diagnosis, indicating higher proliferative and survival potential of leukaemic cells in relapse. Routine analysis of mTOR activity could be performed to select patients that may potentially benefit from mTOR inhibitors (MTI) treatment.
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spelling pubmed-50321562016-09-29 Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia – preliminary report Ulińska, Edyta Mycko, Katarzyna Sałacińska-Łoś, Elżbieta Pastorczak, Agata Siwicka, Alicja Młynarski, Wojciech Matysiak, Michał Contemp Oncol (Pozn) Original Paper AIM OF THE STUDY: To characterise expression of mTOR (mammalian target of rapamycin) in childhood B-cell acute lymphoblastic leukaemia (ALL), and to evaluate a possible link between mTOR and clinical characteristics. MATERIAL AND METHODS: The examined group consisted of 21 consecutive patients, aged 1–18 years, diagnosed with B-cell ALL in 2010, and 10 relapsed B-cell ALL patients diagnosed for the first time between 2009 and 2011, who developed relapse before 2014. All subjects were treated in the Department of Paediatric Haematology and Oncology of the Medical University of Warsaw according to the ALL-IC BFM 2002 Protocol. We evaluated mTOR and phospho-mTOR expression by immunohistochemistry using rabbit monoclonal antibodies. RESULTS: mTOR expression was found to be significantly associated with the risk of relapse and was more frequent in ALL recurrence. No significant relationship was detected between mTOR expression and other features of high-risk disease in paediatric ALL. CONCLUSIONS: mTOR activity could be considered a high-risk feature in paediatric B-cell ALL. Expression of mTOR kinase is observed remarkably more frequently in disease recurrence than at first diagnosis, indicating higher proliferative and survival potential of leukaemic cells in relapse. Routine analysis of mTOR activity could be performed to select patients that may potentially benefit from mTOR inhibitors (MTI) treatment. Termedia Publishing House 2016-09-05 2016 /pmc/articles/PMC5032156/ /pubmed/27688725 http://dx.doi.org/10.5114/wo.2016.61848 Text en Copyright: © 2016 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Ulińska, Edyta
Mycko, Katarzyna
Sałacińska-Łoś, Elżbieta
Pastorczak, Agata
Siwicka, Alicja
Młynarski, Wojciech
Matysiak, Michał
Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia – preliminary report
title Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia – preliminary report
title_full Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia – preliminary report
title_fullStr Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia – preliminary report
title_full_unstemmed Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia – preliminary report
title_short Impact of mTOR expression on clinical outcome in paediatric patients with B-cell acute lymphoblastic leukaemia – preliminary report
title_sort impact of mtor expression on clinical outcome in paediatric patients with b-cell acute lymphoblastic leukaemia – preliminary report
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5032156/
https://www.ncbi.nlm.nih.gov/pubmed/27688725
http://dx.doi.org/10.5114/wo.2016.61848
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