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PTRF/Cavin-1 and MIF Proteins Are Identified as Non-Small Cell Lung Cancer Biomarkers by Label-Free Proteomics

With the completion of the human genome sequence, biomedical sciences have entered in the “omics” era, mainly due to high-throughput genomics techniques and the recent application of mass spectrometry to proteomics analyses. However, there is still a time lag between these technological advances and...

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Autores principales: Gámez-Pozo, Angelo, Sánchez-Navarro, Iker, Calvo, Enrique, Agulló-Ortuño, María Teresa, López-Vacas, Rocío, Díaz, Esther, Camafeita, Emilio, Nistal, Manuel, Madero, Rosario, Espinosa, Enrique, López, Juan Antonio, Vara, Juan Ángel Fresno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312891/
https://www.ncbi.nlm.nih.gov/pubmed/22461895
http://dx.doi.org/10.1371/journal.pone.0033752
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author Gámez-Pozo, Angelo
Sánchez-Navarro, Iker
Calvo, Enrique
Agulló-Ortuño, María Teresa
López-Vacas, Rocío
Díaz, Esther
Camafeita, Emilio
Nistal, Manuel
Madero, Rosario
Espinosa, Enrique
López, Juan Antonio
Vara, Juan Ángel Fresno
author_facet Gámez-Pozo, Angelo
Sánchez-Navarro, Iker
Calvo, Enrique
Agulló-Ortuño, María Teresa
López-Vacas, Rocío
Díaz, Esther
Camafeita, Emilio
Nistal, Manuel
Madero, Rosario
Espinosa, Enrique
López, Juan Antonio
Vara, Juan Ángel Fresno
author_sort Gámez-Pozo, Angelo
collection PubMed
description With the completion of the human genome sequence, biomedical sciences have entered in the “omics” era, mainly due to high-throughput genomics techniques and the recent application of mass spectrometry to proteomics analyses. However, there is still a time lag between these technological advances and their application in the clinical setting. Our work is designed to build bridges between high-performance proteomics and clinical routine. Protein extracts were obtained from fresh frozen normal lung and non-small cell lung cancer samples. We applied a phosphopeptide enrichment followed by LC-MS/MS. Subsequent label-free quantification and bioinformatics analyses were performed. We assessed protein patterns on these samples, showing dozens of differential markers between normal and tumor tissue. Gene ontology and interactome analyses identified signaling pathways altered on tumor tissue. We have identified two proteins, PTRF/cavin-1 and MIF, which are differentially expressed between normal lung and non-small cell lung cancer. These potential biomarkers were validated using western blot and immunohistochemistry. The application of discovery-based proteomics analyses in clinical samples allowed us to identify new potential biomarkers and therapeutic targets in non-small cell lung cancer.
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spelling pubmed-33128912012-03-29 PTRF/Cavin-1 and MIF Proteins Are Identified as Non-Small Cell Lung Cancer Biomarkers by Label-Free Proteomics Gámez-Pozo, Angelo Sánchez-Navarro, Iker Calvo, Enrique Agulló-Ortuño, María Teresa López-Vacas, Rocío Díaz, Esther Camafeita, Emilio Nistal, Manuel Madero, Rosario Espinosa, Enrique López, Juan Antonio Vara, Juan Ángel Fresno PLoS One Research Article With the completion of the human genome sequence, biomedical sciences have entered in the “omics” era, mainly due to high-throughput genomics techniques and the recent application of mass spectrometry to proteomics analyses. However, there is still a time lag between these technological advances and their application in the clinical setting. Our work is designed to build bridges between high-performance proteomics and clinical routine. Protein extracts were obtained from fresh frozen normal lung and non-small cell lung cancer samples. We applied a phosphopeptide enrichment followed by LC-MS/MS. Subsequent label-free quantification and bioinformatics analyses were performed. We assessed protein patterns on these samples, showing dozens of differential markers between normal and tumor tissue. Gene ontology and interactome analyses identified signaling pathways altered on tumor tissue. We have identified two proteins, PTRF/cavin-1 and MIF, which are differentially expressed between normal lung and non-small cell lung cancer. These potential biomarkers were validated using western blot and immunohistochemistry. The application of discovery-based proteomics analyses in clinical samples allowed us to identify new potential biomarkers and therapeutic targets in non-small cell lung cancer. Public Library of Science 2012-03-26 /pmc/articles/PMC3312891/ /pubmed/22461895 http://dx.doi.org/10.1371/journal.pone.0033752 Text en Gámez-Pozo 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gámez-Pozo, Angelo
Sánchez-Navarro, Iker
Calvo, Enrique
Agulló-Ortuño, María Teresa
López-Vacas, Rocío
Díaz, Esther
Camafeita, Emilio
Nistal, Manuel
Madero, Rosario
Espinosa, Enrique
López, Juan Antonio
Vara, Juan Ángel Fresno
PTRF/Cavin-1 and MIF Proteins Are Identified as Non-Small Cell Lung Cancer Biomarkers by Label-Free Proteomics
title PTRF/Cavin-1 and MIF Proteins Are Identified as Non-Small Cell Lung Cancer Biomarkers by Label-Free Proteomics
title_full PTRF/Cavin-1 and MIF Proteins Are Identified as Non-Small Cell Lung Cancer Biomarkers by Label-Free Proteomics
title_fullStr PTRF/Cavin-1 and MIF Proteins Are Identified as Non-Small Cell Lung Cancer Biomarkers by Label-Free Proteomics
title_full_unstemmed PTRF/Cavin-1 and MIF Proteins Are Identified as Non-Small Cell Lung Cancer Biomarkers by Label-Free Proteomics
title_short PTRF/Cavin-1 and MIF Proteins Are Identified as Non-Small Cell Lung Cancer Biomarkers by Label-Free Proteomics
title_sort ptrf/cavin-1 and mif proteins are identified as non-small cell lung cancer biomarkers by label-free proteomics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312891/
https://www.ncbi.nlm.nih.gov/pubmed/22461895
http://dx.doi.org/10.1371/journal.pone.0033752
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