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Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients

Protein expression of Myristoylated alanine-rich C kinase substrate like-1 (MARCKSL1) has been identified as a prognostic factor in lymph-node negative (LN(-)) breast cancer patients. We aim to validate MARCKSL1 protein expression as a prognostic marker for distant metastasis-free survival (DMFS) in...

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Autores principales: Egeland, Nina Gran, Austdal, Marie, van Diermen-Hidle, Bianca, Rewcastle, Emma, Gudlaugsson, Einar G., Baak, Jan P. A., Skaland, Ivar, Janssen, Emiel A. M., Jonsdottir, Kristin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411117/
https://www.ncbi.nlm.nih.gov/pubmed/30856208
http://dx.doi.org/10.1371/journal.pone.0212527
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author Egeland, Nina Gran
Austdal, Marie
van Diermen-Hidle, Bianca
Rewcastle, Emma
Gudlaugsson, Einar G.
Baak, Jan P. A.
Skaland, Ivar
Janssen, Emiel A. M.
Jonsdottir, Kristin
author_facet Egeland, Nina Gran
Austdal, Marie
van Diermen-Hidle, Bianca
Rewcastle, Emma
Gudlaugsson, Einar G.
Baak, Jan P. A.
Skaland, Ivar
Janssen, Emiel A. M.
Jonsdottir, Kristin
author_sort Egeland, Nina Gran
collection PubMed
description Protein expression of Myristoylated alanine-rich C kinase substrate like-1 (MARCKSL1) has been identified as a prognostic factor in lymph-node negative (LN(-)) breast cancer patients. We aim to validate MARCKSL1 protein expression as a prognostic marker for distant metastasis-free survival (DMFS) in a new cohort of LN(-) breast cancer patients. MARCKSL1 expression was evaluated in 151 operable T(1,2)N(0)M(0) LN(-) breast cancer patients by immunohistochemistry. Median follow-up time was 152 months, range 11–189 months. Results were compared with classical prognosticators (age, tumor diameter, grade, estrogen receptor, and proliferation) using single (Kaplan-Meier) and multivariate (Cox model) survival analysis. Thirteen patients (9%) developed distant metastases. With both single and multiple analysis of all features, MARCKSL1 did not show a significant prognostic value for DMFS (p = 0.498). Of the assessed classical prognosticators, only tumor diameter showed prognostic value (hazard ratio 9.3, 95% confidence interval 2.8–31.0, p <0.001). MARCKSL1 expression could not be confirmed as a prognostic factor in this cohort. Possible reasons include changes in diagnostic and treatment guidelines between the discovery and validation cohorts. Further studies are needed to reveal the potential biological role of this protein in breast cancer.
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spelling pubmed-64111172019-04-01 Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients Egeland, Nina Gran Austdal, Marie van Diermen-Hidle, Bianca Rewcastle, Emma Gudlaugsson, Einar G. Baak, Jan P. A. Skaland, Ivar Janssen, Emiel A. M. Jonsdottir, Kristin PLoS One Research Article Protein expression of Myristoylated alanine-rich C kinase substrate like-1 (MARCKSL1) has been identified as a prognostic factor in lymph-node negative (LN(-)) breast cancer patients. We aim to validate MARCKSL1 protein expression as a prognostic marker for distant metastasis-free survival (DMFS) in a new cohort of LN(-) breast cancer patients. MARCKSL1 expression was evaluated in 151 operable T(1,2)N(0)M(0) LN(-) breast cancer patients by immunohistochemistry. Median follow-up time was 152 months, range 11–189 months. Results were compared with classical prognosticators (age, tumor diameter, grade, estrogen receptor, and proliferation) using single (Kaplan-Meier) and multivariate (Cox model) survival analysis. Thirteen patients (9%) developed distant metastases. With both single and multiple analysis of all features, MARCKSL1 did not show a significant prognostic value for DMFS (p = 0.498). Of the assessed classical prognosticators, only tumor diameter showed prognostic value (hazard ratio 9.3, 95% confidence interval 2.8–31.0, p <0.001). MARCKSL1 expression could not be confirmed as a prognostic factor in this cohort. Possible reasons include changes in diagnostic and treatment guidelines between the discovery and validation cohorts. Further studies are needed to reveal the potential biological role of this protein in breast cancer. Public Library of Science 2019-03-11 /pmc/articles/PMC6411117/ /pubmed/30856208 http://dx.doi.org/10.1371/journal.pone.0212527 Text en © 2019 Egeland et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Egeland, Nina Gran
Austdal, Marie
van Diermen-Hidle, Bianca
Rewcastle, Emma
Gudlaugsson, Einar G.
Baak, Jan P. A.
Skaland, Ivar
Janssen, Emiel A. M.
Jonsdottir, Kristin
Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients
title Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients
title_full Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients
title_fullStr Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients
title_full_unstemmed Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients
title_short Validation study of MARCKSL1 as a prognostic factor in lymph node-negative breast cancer patients
title_sort validation study of marcksl1 as a prognostic factor in lymph node-negative breast cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411117/
https://www.ncbi.nlm.nih.gov/pubmed/30856208
http://dx.doi.org/10.1371/journal.pone.0212527
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