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Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines

Cell lines are important models for drug resistance in acute lymphoblastic leukaemia (ALL), but are often criticised as being unrepresentative of primary disease. There are also doubts regarding the authenticity of many lines. We have characterised a panel of ALL cell lines for growth and drug resis...

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Autores principales: Beesley, A H, Palmer, M-L, Ford, J, Weller, R E, Cummings, A J, Freitas, J R, Firth, M J, Perera, K U, de Klerk, N H, Kees, U R
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360743/
https://www.ncbi.nlm.nih.gov/pubmed/17117183
http://dx.doi.org/10.1038/sj.bjc.6603447
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author Beesley, A H
Palmer, M-L
Ford, J
Weller, R E
Cummings, A J
Freitas, J R
Firth, M J
Perera, K U
de Klerk, N H
Kees, U R
author_facet Beesley, A H
Palmer, M-L
Ford, J
Weller, R E
Cummings, A J
Freitas, J R
Firth, M J
Perera, K U
de Klerk, N H
Kees, U R
author_sort Beesley, A H
collection PubMed
description Cell lines are important models for drug resistance in acute lymphoblastic leukaemia (ALL), but are often criticised as being unrepresentative of primary disease. There are also doubts regarding the authenticity of many lines. We have characterised a panel of ALL cell lines for growth and drug resistance and compared data with that published for primary patient specimens. In contrast to the convention that cell lines are highly proliferative, those established in our laboratory grow at rates similar to estimates of leukaemic cells in vivo (doubling time 53–442 h). Authenticity was confirmed by genetic fingerprinting, which also demonstrated the potential stability of long-term cultures. In vitro glucocorticoid resistance correlated well with that measured ex vivo, but all lines were significantly more sensitive to vincristine than primary specimens. Sensitivity to methotrexate was inversely correlated to that of glucocorticoids and L-asparaginase, indicating possible reciprocity in resistance mechanisms. A cell line identified as highly methotrexate resistant (IC(50) >8000-fold higher than other lines) was derived from a patient receiving escalating doses of the drug, indicating in vivo selection of resistance as a cause of relapse. Many of these lines are suitable as models to study naturally occurring resistance phenotypes in paediatric ALL.
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spelling pubmed-23607432009-09-10 Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines Beesley, A H Palmer, M-L Ford, J Weller, R E Cummings, A J Freitas, J R Firth, M J Perera, K U de Klerk, N H Kees, U R Br J Cancer Molecular Diagnostics Cell lines are important models for drug resistance in acute lymphoblastic leukaemia (ALL), but are often criticised as being unrepresentative of primary disease. There are also doubts regarding the authenticity of many lines. We have characterised a panel of ALL cell lines for growth and drug resistance and compared data with that published for primary patient specimens. In contrast to the convention that cell lines are highly proliferative, those established in our laboratory grow at rates similar to estimates of leukaemic cells in vivo (doubling time 53–442 h). Authenticity was confirmed by genetic fingerprinting, which also demonstrated the potential stability of long-term cultures. In vitro glucocorticoid resistance correlated well with that measured ex vivo, but all lines were significantly more sensitive to vincristine than primary specimens. Sensitivity to methotrexate was inversely correlated to that of glucocorticoids and L-asparaginase, indicating possible reciprocity in resistance mechanisms. A cell line identified as highly methotrexate resistant (IC(50) >8000-fold higher than other lines) was derived from a patient receiving escalating doses of the drug, indicating in vivo selection of resistance as a cause of relapse. Many of these lines are suitable as models to study naturally occurring resistance phenotypes in paediatric ALL. Nature Publishing Group 2006-12-04 2006-11-21 /pmc/articles/PMC2360743/ /pubmed/17117183 http://dx.doi.org/10.1038/sj.bjc.6603447 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Beesley, A H
Palmer, M-L
Ford, J
Weller, R E
Cummings, A J
Freitas, J R
Firth, M J
Perera, K U
de Klerk, N H
Kees, U R
Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines
title Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines
title_full Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines
title_fullStr Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines
title_full_unstemmed Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines
title_short Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines
title_sort authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360743/
https://www.ncbi.nlm.nih.gov/pubmed/17117183
http://dx.doi.org/10.1038/sj.bjc.6603447
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