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Immune Condition of Colorectal Cancer Patients Featured by Serum Chemokines and Gene Expressions of CD4+ Cells in Blood
BACKGROUND: Colorectal cancer (CRC), the most common malignancy worldwide, causes inflammation. We explored the inflammatory pathophysiology of CRC by assessing the peripheral blood parameters. METHODS: The differences in gene expression profiles of whole blood cells and cell subpopulations between...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016223/ https://www.ncbi.nlm.nih.gov/pubmed/29992127 http://dx.doi.org/10.1155/2018/7436205 |
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author | Komura, Takuya Yano, Masaaki Miyake, Akimitsu Takabatake, Hisashi Miyazawa, Masaki Ogawa, Norihiko Seki, Akihiro Honda, Masao Wada, Takashi Matsui, Shigeyuki Kaneko, Shuichi Sakai, Yoshio |
author_facet | Komura, Takuya Yano, Masaaki Miyake, Akimitsu Takabatake, Hisashi Miyazawa, Masaki Ogawa, Norihiko Seki, Akihiro Honda, Masao Wada, Takashi Matsui, Shigeyuki Kaneko, Shuichi Sakai, Yoshio |
author_sort | Komura, Takuya |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC), the most common malignancy worldwide, causes inflammation. We explored the inflammatory pathophysiology of CRC by assessing the peripheral blood parameters. METHODS: The differences in gene expression profiles of whole blood cells and cell subpopulations between CRC patients and healthy controls were analyzed using DNA microarray. Serum cytokine/chemokine concentrations in CRC patients and healthy controls were measured via multiplex detection immunoassays. In addition, we explored correlations between the expression levels of certain genes of peripheral CD4+ cells and serum chemokine concentrations. RESULTS: The gene expression profiles of peripheral CD4+ cells of CRC patients differed from those of healthy controls, but this was not true of CD8+ cells, CD14+ cells, CD15+ cells, or CD19+ cells. Serum IL-8 and eotaxin-1 levels were significantly elevated in CRC patients, and the levels substantially correlated with the expression levels of certain genes of CD4+ cells. Interestingly, the relationships between gene expression levels in peripheral CD4+ cells and serum IL-8 and eotaxin-1 levels resembled those of monocytes/macrophages, not T cells. CONCLUSIONS: Serum IL-8 and eotaxin-1 concentrations increased and were associated with changes in the gene expression of peripheral CD4+ cells in CRC patients. |
format | Online Article Text |
id | pubmed-6016223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-60162232018-07-10 Immune Condition of Colorectal Cancer Patients Featured by Serum Chemokines and Gene Expressions of CD4+ Cells in Blood Komura, Takuya Yano, Masaaki Miyake, Akimitsu Takabatake, Hisashi Miyazawa, Masaki Ogawa, Norihiko Seki, Akihiro Honda, Masao Wada, Takashi Matsui, Shigeyuki Kaneko, Shuichi Sakai, Yoshio Can J Gastroenterol Hepatol Research Article BACKGROUND: Colorectal cancer (CRC), the most common malignancy worldwide, causes inflammation. We explored the inflammatory pathophysiology of CRC by assessing the peripheral blood parameters. METHODS: The differences in gene expression profiles of whole blood cells and cell subpopulations between CRC patients and healthy controls were analyzed using DNA microarray. Serum cytokine/chemokine concentrations in CRC patients and healthy controls were measured via multiplex detection immunoassays. In addition, we explored correlations between the expression levels of certain genes of peripheral CD4+ cells and serum chemokine concentrations. RESULTS: The gene expression profiles of peripheral CD4+ cells of CRC patients differed from those of healthy controls, but this was not true of CD8+ cells, CD14+ cells, CD15+ cells, or CD19+ cells. Serum IL-8 and eotaxin-1 levels were significantly elevated in CRC patients, and the levels substantially correlated with the expression levels of certain genes of CD4+ cells. Interestingly, the relationships between gene expression levels in peripheral CD4+ cells and serum IL-8 and eotaxin-1 levels resembled those of monocytes/macrophages, not T cells. CONCLUSIONS: Serum IL-8 and eotaxin-1 concentrations increased and were associated with changes in the gene expression of peripheral CD4+ cells in CRC patients. Hindawi 2018-06-11 /pmc/articles/PMC6016223/ /pubmed/29992127 http://dx.doi.org/10.1155/2018/7436205 Text en Copyright © 2018 Takuya Komura et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Komura, Takuya Yano, Masaaki Miyake, Akimitsu Takabatake, Hisashi Miyazawa, Masaki Ogawa, Norihiko Seki, Akihiro Honda, Masao Wada, Takashi Matsui, Shigeyuki Kaneko, Shuichi Sakai, Yoshio Immune Condition of Colorectal Cancer Patients Featured by Serum Chemokines and Gene Expressions of CD4+ Cells in Blood |
title | Immune Condition of Colorectal Cancer Patients Featured by Serum Chemokines and Gene Expressions of CD4+ Cells in Blood |
title_full | Immune Condition of Colorectal Cancer Patients Featured by Serum Chemokines and Gene Expressions of CD4+ Cells in Blood |
title_fullStr | Immune Condition of Colorectal Cancer Patients Featured by Serum Chemokines and Gene Expressions of CD4+ Cells in Blood |
title_full_unstemmed | Immune Condition of Colorectal Cancer Patients Featured by Serum Chemokines and Gene Expressions of CD4+ Cells in Blood |
title_short | Immune Condition of Colorectal Cancer Patients Featured by Serum Chemokines and Gene Expressions of CD4+ Cells in Blood |
title_sort | immune condition of colorectal cancer patients featured by serum chemokines and gene expressions of cd4+ cells in blood |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016223/ https://www.ncbi.nlm.nih.gov/pubmed/29992127 http://dx.doi.org/10.1155/2018/7436205 |
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