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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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