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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...

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Autores principales: Komura, Takuya, Yano, Masaaki, Miyake, Akimitsu, Takabatake, Hisashi, Miyazawa, Masaki, Ogawa, Norihiko, Seki, Akihiro, Honda, Masao, Wada, Takashi, Matsui, Shigeyuki, Kaneko, Shuichi, Sakai, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
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.
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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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