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OLFM4, KNG1 and Sec24C identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages
BACKGROUND: Despite recent advances in colorectal cancer (CRC) diagnosis and population screening programs, the identification of patients with preneoplastic lesions or with early CRC stages remains challenging and is important for reducing CRC incidence and increasing patient’s survival. METHODS: W...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364649/ https://www.ncbi.nlm.nih.gov/pubmed/28344541 http://dx.doi.org/10.1186/s12014-017-9143-3 |
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author | Quesada-Calvo, Florence Massot, Charlotte Bertrand, Virginie Longuespée, Rémi Blétard, Noëlla Somja, Joan Mazzucchelli, Gabriel Smargiasso, Nicolas Baiwir, Dominique De Pauw-Gillet, Marie-Claire Delvenne, Philippe Malaise, Michel Coimbra Marques, Carla Polus, Marc De Pauw, Edwin Meuwis, Marie-Alice Louis, Edouard |
author_facet | Quesada-Calvo, Florence Massot, Charlotte Bertrand, Virginie Longuespée, Rémi Blétard, Noëlla Somja, Joan Mazzucchelli, Gabriel Smargiasso, Nicolas Baiwir, Dominique De Pauw-Gillet, Marie-Claire Delvenne, Philippe Malaise, Michel Coimbra Marques, Carla Polus, Marc De Pauw, Edwin Meuwis, Marie-Alice Louis, Edouard |
author_sort | Quesada-Calvo, Florence |
collection | PubMed |
description | BACKGROUND: Despite recent advances in colorectal cancer (CRC) diagnosis and population screening programs, the identification of patients with preneoplastic lesions or with early CRC stages remains challenging and is important for reducing CRC incidence and increasing patient’s survival. METHODS: We analysed 76 colorectal tissue samples originated from early CRC stages, normal or inflamed mucosa by label-free proteomics. The characterisation of three selected biomarker candidates was performed by immunohistochemistry on an independent set of precancerous and cancerous lesions harbouring increasing CRC stages. RESULTS: Out of 5258 proteins identified, we obtained 561 proteins with a significant differential distribution among groups of patients and controls. KNG1, OLFM4 and Sec24C distributions were validated in tissues and showed different expression levels especially in the two early CRC stages compared to normal and preneoplastic tissues. CONCLUSION: We highlighted three proteins that require further investigations to better characterise their role in early CRC carcinogenesis and their potential as early CRC markers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12014-017-9143-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5364649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53646492017-03-24 OLFM4, KNG1 and Sec24C identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages Quesada-Calvo, Florence Massot, Charlotte Bertrand, Virginie Longuespée, Rémi Blétard, Noëlla Somja, Joan Mazzucchelli, Gabriel Smargiasso, Nicolas Baiwir, Dominique De Pauw-Gillet, Marie-Claire Delvenne, Philippe Malaise, Michel Coimbra Marques, Carla Polus, Marc De Pauw, Edwin Meuwis, Marie-Alice Louis, Edouard Clin Proteomics Research BACKGROUND: Despite recent advances in colorectal cancer (CRC) diagnosis and population screening programs, the identification of patients with preneoplastic lesions or with early CRC stages remains challenging and is important for reducing CRC incidence and increasing patient’s survival. METHODS: We analysed 76 colorectal tissue samples originated from early CRC stages, normal or inflamed mucosa by label-free proteomics. The characterisation of three selected biomarker candidates was performed by immunohistochemistry on an independent set of precancerous and cancerous lesions harbouring increasing CRC stages. RESULTS: Out of 5258 proteins identified, we obtained 561 proteins with a significant differential distribution among groups of patients and controls. KNG1, OLFM4 and Sec24C distributions were validated in tissues and showed different expression levels especially in the two early CRC stages compared to normal and preneoplastic tissues. CONCLUSION: We highlighted three proteins that require further investigations to better characterise their role in early CRC carcinogenesis and their potential as early CRC markers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12014-017-9143-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-24 /pmc/articles/PMC5364649/ /pubmed/28344541 http://dx.doi.org/10.1186/s12014-017-9143-3 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Quesada-Calvo, Florence Massot, Charlotte Bertrand, Virginie Longuespée, Rémi Blétard, Noëlla Somja, Joan Mazzucchelli, Gabriel Smargiasso, Nicolas Baiwir, Dominique De Pauw-Gillet, Marie-Claire Delvenne, Philippe Malaise, Michel Coimbra Marques, Carla Polus, Marc De Pauw, Edwin Meuwis, Marie-Alice Louis, Edouard OLFM4, KNG1 and Sec24C identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages |
title | OLFM4, KNG1 and Sec24C identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages |
title_full | OLFM4, KNG1 and Sec24C identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages |
title_fullStr | OLFM4, KNG1 and Sec24C identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages |
title_full_unstemmed | OLFM4, KNG1 and Sec24C identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages |
title_short | OLFM4, KNG1 and Sec24C identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages |
title_sort | olfm4, kng1 and sec24c identified by proteomics and immunohistochemistry as potential markers of early colorectal cancer stages |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364649/ https://www.ncbi.nlm.nih.gov/pubmed/28344541 http://dx.doi.org/10.1186/s12014-017-9143-3 |
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