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HLA-G Expression in Tumor Tissues and Soluble HLA-G Plasma Levels in Patients with Gastrointestinal Cancer

BACKGROUND: Overexpression of human leukocyte antigen G (HLA-G) and increased plasma levels of soluble HLA-G (sHLA-G) have been reported in different human malignancies, and are believed to be involved in tumor immune evasion. OBJECTIVES: This study was designed to evaluate the expression of HLA-G i...

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Autores principales: Farjadian, Shirin, Tabebordbar, Maryam, Mokhtari, Maral, Safaei, Akbar, Malekzadeh, Mahyar, Ghaderi, Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291033/
https://www.ncbi.nlm.nih.gov/pubmed/30360598
http://dx.doi.org/10.22034/APJCP.2018.19.10.2731
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author Farjadian, Shirin
Tabebordbar, Maryam
Mokhtari, Maral
Safaei, Akbar
Malekzadeh, Mahyar
Ghaderi, Abbas
author_facet Farjadian, Shirin
Tabebordbar, Maryam
Mokhtari, Maral
Safaei, Akbar
Malekzadeh, Mahyar
Ghaderi, Abbas
author_sort Farjadian, Shirin
collection PubMed
description BACKGROUND: Overexpression of human leukocyte antigen G (HLA-G) and increased plasma levels of soluble HLA-G (sHLA-G) have been reported in different human malignancies, and are believed to be involved in tumor immune evasion. OBJECTIVES: This study was designed to evaluate the expression of HLA-G in tumor tissues and the plasma levels of sHLA-G in patients with gastrointestinal cancer, and to determine their associations with clinicopathological factors. The link between Helicobacter pylori infection and increased HLA-G expression or sHLA-G levels was also investigated in patients with gastric cancer. METHODS: HLA-G expression was investigated in tumor tissues from 100 patients with gastric and colorectal adenocarcinoma using immunohistochemistry test, and plasma levels of sHLA-G were measured in 82 patients with ELISA method. The presence of H. pylori genome was investigated in tumor tissues from 25 patients with gastric cancer by PCR method. RESULTS: HLA-G expression was observed in 43% of colorectal cancers and 34.6% of gastric cancers, and was not related with any of the clinicopathological factors. There was a significant correlation between increased sHLA-G level and stage I tumors. Eight of 25 (32%) gastric cancer specimens were positive for H. pylori, of which 3 samples were positive for HLA-G. Soluble HLA-G levels were above the cut-off value in all H. pylori-positive patients. CONCLUSION: Plasma levels of sHLA-G were significantly increased in our patients with a sensitivity of 89% and a specificity of 62%. Soluble HLA-G level can be considered a useful indicator for the early diagnosis of gastric and colorectal adenocarcinoma.
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spelling pubmed-62910332018-12-26 HLA-G Expression in Tumor Tissues and Soluble HLA-G Plasma Levels in Patients with Gastrointestinal Cancer Farjadian, Shirin Tabebordbar, Maryam Mokhtari, Maral Safaei, Akbar Malekzadeh, Mahyar Ghaderi, Abbas Asian Pac J Cancer Prev Research Article BACKGROUND: Overexpression of human leukocyte antigen G (HLA-G) and increased plasma levels of soluble HLA-G (sHLA-G) have been reported in different human malignancies, and are believed to be involved in tumor immune evasion. OBJECTIVES: This study was designed to evaluate the expression of HLA-G in tumor tissues and the plasma levels of sHLA-G in patients with gastrointestinal cancer, and to determine their associations with clinicopathological factors. The link between Helicobacter pylori infection and increased HLA-G expression or sHLA-G levels was also investigated in patients with gastric cancer. METHODS: HLA-G expression was investigated in tumor tissues from 100 patients with gastric and colorectal adenocarcinoma using immunohistochemistry test, and plasma levels of sHLA-G were measured in 82 patients with ELISA method. The presence of H. pylori genome was investigated in tumor tissues from 25 patients with gastric cancer by PCR method. RESULTS: HLA-G expression was observed in 43% of colorectal cancers and 34.6% of gastric cancers, and was not related with any of the clinicopathological factors. There was a significant correlation between increased sHLA-G level and stage I tumors. Eight of 25 (32%) gastric cancer specimens were positive for H. pylori, of which 3 samples were positive for HLA-G. Soluble HLA-G levels were above the cut-off value in all H. pylori-positive patients. CONCLUSION: Plasma levels of sHLA-G were significantly increased in our patients with a sensitivity of 89% and a specificity of 62%. Soluble HLA-G level can be considered a useful indicator for the early diagnosis of gastric and colorectal adenocarcinoma. West Asia Organization for Cancer Prevention 2018 /pmc/articles/PMC6291033/ /pubmed/30360598 http://dx.doi.org/10.22034/APJCP.2018.19.10.2731 Text en Copyright: © Asian Pacific Journal of Cancer Prevention http://creativecommons.org/licenses/BY-SA/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Research Article
Farjadian, Shirin
Tabebordbar, Maryam
Mokhtari, Maral
Safaei, Akbar
Malekzadeh, Mahyar
Ghaderi, Abbas
HLA-G Expression in Tumor Tissues and Soluble HLA-G Plasma Levels in Patients with Gastrointestinal Cancer
title HLA-G Expression in Tumor Tissues and Soluble HLA-G Plasma Levels in Patients with Gastrointestinal Cancer
title_full HLA-G Expression in Tumor Tissues and Soluble HLA-G Plasma Levels in Patients with Gastrointestinal Cancer
title_fullStr HLA-G Expression in Tumor Tissues and Soluble HLA-G Plasma Levels in Patients with Gastrointestinal Cancer
title_full_unstemmed HLA-G Expression in Tumor Tissues and Soluble HLA-G Plasma Levels in Patients with Gastrointestinal Cancer
title_short HLA-G Expression in Tumor Tissues and Soluble HLA-G Plasma Levels in Patients with Gastrointestinal Cancer
title_sort hla-g expression in tumor tissues and soluble hla-g plasma levels in patients with gastrointestinal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291033/
https://www.ncbi.nlm.nih.gov/pubmed/30360598
http://dx.doi.org/10.22034/APJCP.2018.19.10.2731
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