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Genetic 3′UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients

The study describes a relationship between the 3′UTR variants, clinicopathological parameters and response to chemotherapy. We analyzed 33 germline polymorphisms in 3′UTRs of ADME genes in 305 breast cancer women treated with FAC regime. Clinical endpoints of this study were: overall survival (OS),...

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Autores principales: Pamuła-Piłat, Jolanta, Tęcza, Karolina, Kalinowska-Herok, Magdalena, Grzybowska, Ewa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109149/
https://www.ncbi.nlm.nih.gov/pubmed/32235849
http://dx.doi.org/10.1038/s41598-020-62662-z
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author Pamuła-Piłat, Jolanta
Tęcza, Karolina
Kalinowska-Herok, Magdalena
Grzybowska, Ewa
author_facet Pamuła-Piłat, Jolanta
Tęcza, Karolina
Kalinowska-Herok, Magdalena
Grzybowska, Ewa
author_sort Pamuła-Piłat, Jolanta
collection PubMed
description The study describes a relationship between the 3′UTR variants, clinicopathological parameters and response to chemotherapy. We analyzed 33 germline polymorphisms in 3′UTRs of ADME genes in 305 breast cancer women treated with FAC regime. Clinical endpoints of this study were: overall survival (OS), progression-free survival (PFS), recurrence-free survival (RFS) and overall response defined as treatment failure-free survival (TFFS). The shortened OS was connected with the presence of NR1/2 rs3732359 AA, SLC22A16 rs7756222 CC, as well as SLC22A16 rs9487402 allele G and clinical factors belonging to TNM classification: tumor size >1 cm, nodal involvement and presence of metastases. PFS was related to two polymorphisms PGR rs1824125 GG, PGR rs12224560 CC and SLC22A16 rs7756222 CC as well as preexisting metastases. The RFS was shortened due to the DPYD rs291593 CC, AKR1C3 rs3209896 AG and negative expression of PGR. The presence of ALDH5A1 rs1054899 allele A, lack of pre-chemotherapy surgery and negative status of PGR correlated with worse treatment response. The germline variants commonly present in the population are important factors determining the response to treatment. We observed the effect of the accumulation of genetic and clinical factors on poor survival prognosis and overall treatment response.
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spelling pubmed-71091492020-04-06 Genetic 3′UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients Pamuła-Piłat, Jolanta Tęcza, Karolina Kalinowska-Herok, Magdalena Grzybowska, Ewa Sci Rep Article The study describes a relationship between the 3′UTR variants, clinicopathological parameters and response to chemotherapy. We analyzed 33 germline polymorphisms in 3′UTRs of ADME genes in 305 breast cancer women treated with FAC regime. Clinical endpoints of this study were: overall survival (OS), progression-free survival (PFS), recurrence-free survival (RFS) and overall response defined as treatment failure-free survival (TFFS). The shortened OS was connected with the presence of NR1/2 rs3732359 AA, SLC22A16 rs7756222 CC, as well as SLC22A16 rs9487402 allele G and clinical factors belonging to TNM classification: tumor size >1 cm, nodal involvement and presence of metastases. PFS was related to two polymorphisms PGR rs1824125 GG, PGR rs12224560 CC and SLC22A16 rs7756222 CC as well as preexisting metastases. The RFS was shortened due to the DPYD rs291593 CC, AKR1C3 rs3209896 AG and negative expression of PGR. The presence of ALDH5A1 rs1054899 allele A, lack of pre-chemotherapy surgery and negative status of PGR correlated with worse treatment response. The germline variants commonly present in the population are important factors determining the response to treatment. We observed the effect of the accumulation of genetic and clinical factors on poor survival prognosis and overall treatment response. Nature Publishing Group UK 2020-03-31 /pmc/articles/PMC7109149/ /pubmed/32235849 http://dx.doi.org/10.1038/s41598-020-62662-z Text en © The Author(s) 2020 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/.
spellingShingle Article
Pamuła-Piłat, Jolanta
Tęcza, Karolina
Kalinowska-Herok, Magdalena
Grzybowska, Ewa
Genetic 3′UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients
title Genetic 3′UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients
title_full Genetic 3′UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients
title_fullStr Genetic 3′UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients
title_full_unstemmed Genetic 3′UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients
title_short Genetic 3′UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients
title_sort genetic 3′utr variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109149/
https://www.ncbi.nlm.nih.gov/pubmed/32235849
http://dx.doi.org/10.1038/s41598-020-62662-z
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