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DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship?
Hepatotoxicity is a frequent complication during maintenance therapy of acute lymphoblastic leukemia (ALL) with 6-mercaptopurine and methotrexate. Elevated levels of methylated 6-mercaptopurine metabolites (MeMP) are associated with hepatotoxicity. However, not all mechanisms are known that lead to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506908/ https://www.ncbi.nlm.nih.gov/pubmed/37138020 http://dx.doi.org/10.1038/s41397-023-00303-0 |
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author | Harju, Tekla Hurme-Niiranen, Anri Suo-Palosaari, Maria Nygaard Nielsen, Stine Hinttala, Reetta Schmiegelow, Kjeld Uusimaa, Johanna Harila, Arja Niinimäki, Riitta |
author_facet | Harju, Tekla Hurme-Niiranen, Anri Suo-Palosaari, Maria Nygaard Nielsen, Stine Hinttala, Reetta Schmiegelow, Kjeld Uusimaa, Johanna Harila, Arja Niinimäki, Riitta |
author_sort | Harju, Tekla |
collection | PubMed |
description | Hepatotoxicity is a frequent complication during maintenance therapy of acute lymphoblastic leukemia (ALL) with 6-mercaptopurine and methotrexate. Elevated levels of methylated 6-mercaptopurine metabolites (MeMP) are associated with hepatotoxicity. However, not all mechanisms are known that lead to liver failure in patients with ALL. Variants in the POLG gene, which encodes the catalytic subunit of mitochondrial DNA polymerase gamma (POLG1), have been related to drug-induced hepatotoxicity, for example, by sodium valproate. The association of common POLG variants with hepatotoxicity during maintenance therapy was studied in 34 patients with childhood ALL. Of the screened POLG variants, four different variants were detected in 12 patients. One patient developed severe hepatotoxicity without elevated MeMP levels and harbored a heterozygous POLG p.G517V variant, which was not found in the other patients. [Image: see text] |
format | Online Article Text |
id | pubmed-10506908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105069082023-09-20 DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? Harju, Tekla Hurme-Niiranen, Anri Suo-Palosaari, Maria Nygaard Nielsen, Stine Hinttala, Reetta Schmiegelow, Kjeld Uusimaa, Johanna Harila, Arja Niinimäki, Riitta Pharmacogenomics J Article Hepatotoxicity is a frequent complication during maintenance therapy of acute lymphoblastic leukemia (ALL) with 6-mercaptopurine and methotrexate. Elevated levels of methylated 6-mercaptopurine metabolites (MeMP) are associated with hepatotoxicity. However, not all mechanisms are known that lead to liver failure in patients with ALL. Variants in the POLG gene, which encodes the catalytic subunit of mitochondrial DNA polymerase gamma (POLG1), have been related to drug-induced hepatotoxicity, for example, by sodium valproate. The association of common POLG variants with hepatotoxicity during maintenance therapy was studied in 34 patients with childhood ALL. Of the screened POLG variants, four different variants were detected in 12 patients. One patient developed severe hepatotoxicity without elevated MeMP levels and harbored a heterozygous POLG p.G517V variant, which was not found in the other patients. [Image: see text] Nature Publishing Group UK 2023-05-03 2023 /pmc/articles/PMC10506908/ /pubmed/37138020 http://dx.doi.org/10.1038/s41397-023-00303-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access 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 http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Harju, Tekla Hurme-Niiranen, Anri Suo-Palosaari, Maria Nygaard Nielsen, Stine Hinttala, Reetta Schmiegelow, Kjeld Uusimaa, Johanna Harila, Arja Niinimäki, Riitta DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? |
title | DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? |
title_full | DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? |
title_fullStr | DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? |
title_full_unstemmed | DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? |
title_short | DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? |
title_sort | dna polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506908/ https://www.ncbi.nlm.nih.gov/pubmed/37138020 http://dx.doi.org/10.1038/s41397-023-00303-0 |
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