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L1 cell adhesion molecule (L1CAM) is a strong predictor for locoregional recurrences in cervical cancer
BACKGROUND: L1 cell adhesion molecule (L1CAM) has been shown to be a prognostic marker in various cancer types, and has been suggested to play a role in epithelial mesenchymal transition (EMT). Here, we determined the prognostic significance of L1CAM in cervical cancer and its association with vimen...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5675654/ https://www.ncbi.nlm.nih.gov/pubmed/29152102 http://dx.doi.org/10.18632/oncotarget.20976 |
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author | Schrevel, Marlies Corver, Willem E. Vegter, Margit E. Ter Haar, Natalja T. Dreef, Enno J. Beltman, Jogchum J. Kenter, Gemma Bosse, Tjalling de Kroon, Cornelis D. Jordanova, Ekaterina S. |
author_facet | Schrevel, Marlies Corver, Willem E. Vegter, Margit E. Ter Haar, Natalja T. Dreef, Enno J. Beltman, Jogchum J. Kenter, Gemma Bosse, Tjalling de Kroon, Cornelis D. Jordanova, Ekaterina S. |
author_sort | Schrevel, Marlies |
collection | PubMed |
description | BACKGROUND: L1 cell adhesion molecule (L1CAM) has been shown to be a prognostic marker in various cancer types, and has been suggested to play a role in epithelial mesenchymal transition (EMT). Here, we determined the prognostic significance of L1CAM in cervical cancer and its association with vimentin expression on tumor cells, indicative of EMT. METHODS: Formalin-fixed, paraffin-embedded primary tumor samples from 372 cervical cancer patients were collected for immunohistochemical analysis of L1CAM expression. In 109 FFPE specimens, the percentage of vimentin expressing tumor cells was determined by flow cytometry. RESULTS: Positive L1CAM expression (≥10% of tumor cells) was associated with disease-free survival, validated using RNAseq TCGA data. L1CAM expression was independently associated with locoregional recurrence-free survival (hazard ratio 2.62, 95% CI 1.33 – 5.17, P = 0.006), and strongly associated with percentage of vimentin expressing tumor cells (P = 0.003). Expression of both L1CAM and vimentin indicated a subgroup with the highest risk of recurrence (hazard ratio 3.15, 95% CI 1.25 – 7.92, P = 0.015). CONCLUSION: L1CAM might be a promising new prognostic marker for locoregional recurrences in cervical cancer, and its association with vimentin expression suggests that L1CAM might affect tumor aggressiveness, possibly through EMT. |
format | Online Article Text |
id | pubmed-5675654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56756542017-11-18 L1 cell adhesion molecule (L1CAM) is a strong predictor for locoregional recurrences in cervical cancer Schrevel, Marlies Corver, Willem E. Vegter, Margit E. Ter Haar, Natalja T. Dreef, Enno J. Beltman, Jogchum J. Kenter, Gemma Bosse, Tjalling de Kroon, Cornelis D. Jordanova, Ekaterina S. Oncotarget Research Paper BACKGROUND: L1 cell adhesion molecule (L1CAM) has been shown to be a prognostic marker in various cancer types, and has been suggested to play a role in epithelial mesenchymal transition (EMT). Here, we determined the prognostic significance of L1CAM in cervical cancer and its association with vimentin expression on tumor cells, indicative of EMT. METHODS: Formalin-fixed, paraffin-embedded primary tumor samples from 372 cervical cancer patients were collected for immunohistochemical analysis of L1CAM expression. In 109 FFPE specimens, the percentage of vimentin expressing tumor cells was determined by flow cytometry. RESULTS: Positive L1CAM expression (≥10% of tumor cells) was associated with disease-free survival, validated using RNAseq TCGA data. L1CAM expression was independently associated with locoregional recurrence-free survival (hazard ratio 2.62, 95% CI 1.33 – 5.17, P = 0.006), and strongly associated with percentage of vimentin expressing tumor cells (P = 0.003). Expression of both L1CAM and vimentin indicated a subgroup with the highest risk of recurrence (hazard ratio 3.15, 95% CI 1.25 – 7.92, P = 0.015). CONCLUSION: L1CAM might be a promising new prognostic marker for locoregional recurrences in cervical cancer, and its association with vimentin expression suggests that L1CAM might affect tumor aggressiveness, possibly through EMT. Impact Journals LLC 2017-09-18 /pmc/articles/PMC5675654/ /pubmed/29152102 http://dx.doi.org/10.18632/oncotarget.20976 Text en Copyright: © 2017 Schrevel et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Schrevel, Marlies Corver, Willem E. Vegter, Margit E. Ter Haar, Natalja T. Dreef, Enno J. Beltman, Jogchum J. Kenter, Gemma Bosse, Tjalling de Kroon, Cornelis D. Jordanova, Ekaterina S. L1 cell adhesion molecule (L1CAM) is a strong predictor for locoregional recurrences in cervical cancer |
title | L1 cell adhesion molecule (L1CAM) is a strong predictor for locoregional recurrences in cervical cancer |
title_full | L1 cell adhesion molecule (L1CAM) is a strong predictor for locoregional recurrences in cervical cancer |
title_fullStr | L1 cell adhesion molecule (L1CAM) is a strong predictor for locoregional recurrences in cervical cancer |
title_full_unstemmed | L1 cell adhesion molecule (L1CAM) is a strong predictor for locoregional recurrences in cervical cancer |
title_short | L1 cell adhesion molecule (L1CAM) is a strong predictor for locoregional recurrences in cervical cancer |
title_sort | l1 cell adhesion molecule (l1cam) is a strong predictor for locoregional recurrences in cervical cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5675654/ https://www.ncbi.nlm.nih.gov/pubmed/29152102 http://dx.doi.org/10.18632/oncotarget.20976 |
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