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Proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer
BACKGROUND: Breast cancer (BC) is the most frequent tumour in women. Triple negative tumours (TNBC)–which are associated with minor survival rates—lack markers predictive of response to anticancer drugs. Triple negative tumours frequently metastasise to the central nervous system (CNS). OBJECTIVE: T...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cancer Intelligence
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369972/ https://www.ncbi.nlm.nih.gov/pubmed/30792808 http://dx.doi.org/10.3332/ecancer.2019.891 |
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author | Rojas L, Katerin Trilla-Fuertes, Lucía Gámez-Pozo, Angelo Chiva, Cristina Sepúlveda, Juan Manso, Luis Prado-Vázquez, Guillermo Zapater-Moros, Andrea López-Vacas, Rocío Ferrer-Gómez, María Mendiola, César Espinosa, Enrique Sabidó, Eduard Ciruelos, Eva Vara, Juan Ángel Fresno |
author_facet | Rojas L, Katerin Trilla-Fuertes, Lucía Gámez-Pozo, Angelo Chiva, Cristina Sepúlveda, Juan Manso, Luis Prado-Vázquez, Guillermo Zapater-Moros, Andrea López-Vacas, Rocío Ferrer-Gómez, María Mendiola, César Espinosa, Enrique Sabidó, Eduard Ciruelos, Eva Vara, Juan Ángel Fresno |
author_sort | Rojas L, Katerin |
collection | PubMed |
description | BACKGROUND: Breast cancer (BC) is the most frequent tumour in women. Triple negative tumours (TNBC)–which are associated with minor survival rates—lack markers predictive of response to anticancer drugs. Triple negative tumours frequently metastasise to the central nervous system (CNS). OBJECTIVE: The main objective of this study was to study differences in tumour protein expression between patients with CNS metastases and those without this kind of spread, and propose new biomarkers. METHODS: A retrospective study was performed. Targeted proteomics and statistical analyses were used to identify possible biomarkers. RESULTS: Proteins were quantified by a targeted proteomics approach and protein expression data were successfully obtained from 51 triple negative formalin-fixed paraffin-embedded samples. ISG15, THBS1 and AP1M1 were identified as possible biomarkers related with CNS metastasis development. CONCLUSIONS: Three possible biomarkers associated with CNS metastases in TNBC tumours were identified: ISG15, THBS1 and AP1M1. They may become markers predicting the appearance of CNS infiltration in triple negative BC. |
format | Online Article Text |
id | pubmed-6369972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cancer Intelligence |
record_format | MEDLINE/PubMed |
spelling | pubmed-63699722019-02-21 Proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer Rojas L, Katerin Trilla-Fuertes, Lucía Gámez-Pozo, Angelo Chiva, Cristina Sepúlveda, Juan Manso, Luis Prado-Vázquez, Guillermo Zapater-Moros, Andrea López-Vacas, Rocío Ferrer-Gómez, María Mendiola, César Espinosa, Enrique Sabidó, Eduard Ciruelos, Eva Vara, Juan Ángel Fresno Ecancermedicalscience Research BACKGROUND: Breast cancer (BC) is the most frequent tumour in women. Triple negative tumours (TNBC)–which are associated with minor survival rates—lack markers predictive of response to anticancer drugs. Triple negative tumours frequently metastasise to the central nervous system (CNS). OBJECTIVE: The main objective of this study was to study differences in tumour protein expression between patients with CNS metastases and those without this kind of spread, and propose new biomarkers. METHODS: A retrospective study was performed. Targeted proteomics and statistical analyses were used to identify possible biomarkers. RESULTS: Proteins were quantified by a targeted proteomics approach and protein expression data were successfully obtained from 51 triple negative formalin-fixed paraffin-embedded samples. ISG15, THBS1 and AP1M1 were identified as possible biomarkers related with CNS metastasis development. CONCLUSIONS: Three possible biomarkers associated with CNS metastases in TNBC tumours were identified: ISG15, THBS1 and AP1M1. They may become markers predicting the appearance of CNS infiltration in triple negative BC. Cancer Intelligence 2019-01-15 /pmc/articles/PMC6369972/ /pubmed/30792808 http://dx.doi.org/10.3332/ecancer.2019.891 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Rojas L, Katerin Trilla-Fuertes, Lucía Gámez-Pozo, Angelo Chiva, Cristina Sepúlveda, Juan Manso, Luis Prado-Vázquez, Guillermo Zapater-Moros, Andrea López-Vacas, Rocío Ferrer-Gómez, María Mendiola, César Espinosa, Enrique Sabidó, Eduard Ciruelos, Eva Vara, Juan Ángel Fresno Proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer |
title | Proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer |
title_full | Proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer |
title_fullStr | Proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer |
title_full_unstemmed | Proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer |
title_short | Proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer |
title_sort | proteomics characterisation of central nervous system metastasis biomarkers in triple negative breast cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369972/ https://www.ncbi.nlm.nih.gov/pubmed/30792808 http://dx.doi.org/10.3332/ecancer.2019.891 |
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