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Identification of aldolase A as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue
Colorectal cancer (CRC) is one of the most common cancers worldwide, and many patients are already at an advanced stage when they are diagnosed. Therefore, novel biomarkers for early detection of colorectal cancer are required. In this study, we performed a global shotgun proteomic analysis using fo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097088/ https://www.ncbi.nlm.nih.gov/pubmed/27468721 http://dx.doi.org/10.1007/s13277-016-5275-8 |
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author | Yamamoto, Tetsushi Kudo, Mitsuhiro Peng, Wei-Xia Takata, Hideyuki Takakura, Hideki Teduka, Kiyoshi Fujii, Takenori Mitamura, Kuniko Taga, Atsushi Uchida, Eiji Naito, Zenya |
author_facet | Yamamoto, Tetsushi Kudo, Mitsuhiro Peng, Wei-Xia Takata, Hideyuki Takakura, Hideki Teduka, Kiyoshi Fujii, Takenori Mitamura, Kuniko Taga, Atsushi Uchida, Eiji Naito, Zenya |
author_sort | Yamamoto, Tetsushi |
collection | PubMed |
description | Colorectal cancer (CRC) is one of the most common cancers worldwide, and many patients are already at an advanced stage when they are diagnosed. Therefore, novel biomarkers for early detection of colorectal cancer are required. In this study, we performed a global shotgun proteomic analysis using formalin-fixed and paraffin-embedded (FFPE) CRC tissue. We identified 84 candidate proteins whose expression levels were differentially expressed in cancer and non-cancer regions. A label-free semiquantitative method based on spectral counting and gene ontology (GO) analysis led to a total of 21 candidate proteins that could potentially be detected in blood. Validation studies revealed cyclophilin A, annexin A2, and aldolase A mRNA and protein expression levels were significantly higher in cancer regions than in non-cancer regions. Moreover, an in vitro study showed that secretion of aldolase A into the culture medium was clearly suppressed in CRC cells compared to normal colon epithelium. These findings suggest that decreased aldolase A in blood may be a novel biomarker for the early detection of CRC. |
format | Online Article Text |
id | pubmed-5097088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-50970882016-11-21 Identification of aldolase A as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue Yamamoto, Tetsushi Kudo, Mitsuhiro Peng, Wei-Xia Takata, Hideyuki Takakura, Hideki Teduka, Kiyoshi Fujii, Takenori Mitamura, Kuniko Taga, Atsushi Uchida, Eiji Naito, Zenya Tumour Biol Original Article Colorectal cancer (CRC) is one of the most common cancers worldwide, and many patients are already at an advanced stage when they are diagnosed. Therefore, novel biomarkers for early detection of colorectal cancer are required. In this study, we performed a global shotgun proteomic analysis using formalin-fixed and paraffin-embedded (FFPE) CRC tissue. We identified 84 candidate proteins whose expression levels were differentially expressed in cancer and non-cancer regions. A label-free semiquantitative method based on spectral counting and gene ontology (GO) analysis led to a total of 21 candidate proteins that could potentially be detected in blood. Validation studies revealed cyclophilin A, annexin A2, and aldolase A mRNA and protein expression levels were significantly higher in cancer regions than in non-cancer regions. Moreover, an in vitro study showed that secretion of aldolase A into the culture medium was clearly suppressed in CRC cells compared to normal colon epithelium. These findings suggest that decreased aldolase A in blood may be a novel biomarker for the early detection of CRC. Springer Netherlands 2016-07-28 /pmc/articles/PMC5097088/ /pubmed/27468721 http://dx.doi.org/10.1007/s13277-016-5275-8 Text en © The Author(s) 2016 Open Access This 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. |
spellingShingle | Original Article Yamamoto, Tetsushi Kudo, Mitsuhiro Peng, Wei-Xia Takata, Hideyuki Takakura, Hideki Teduka, Kiyoshi Fujii, Takenori Mitamura, Kuniko Taga, Atsushi Uchida, Eiji Naito, Zenya Identification of aldolase A as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue |
title | Identification of aldolase A as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue |
title_full | Identification of aldolase A as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue |
title_fullStr | Identification of aldolase A as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue |
title_full_unstemmed | Identification of aldolase A as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue |
title_short | Identification of aldolase A as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue |
title_sort | identification of aldolase a as a potential diagnostic biomarker for colorectal cancer based on proteomic analysis using formalin-fixed paraffin-embedded tissue |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097088/ https://www.ncbi.nlm.nih.gov/pubmed/27468721 http://dx.doi.org/10.1007/s13277-016-5275-8 |
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