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Increased HMGB1 expression correlates with higher expression of c-IAP2 and pERK in colorectal cancer
The aim of this study was to investigate the relationship between high-mobility group box 1 (HMGB1) and colorectal cancer (CRC). In this prospective study, patients with CRC undergoing primary surgery and healthy subjects (control group) were enrolled from July 2013 to December 2014. The serum HMGB1...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370169/ https://www.ncbi.nlm.nih.gov/pubmed/30653121 http://dx.doi.org/10.1097/MD.0000000000014069 |
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author | Zhang, Wenjia An, Fangmei Xia, Min Zhan, Qiang Tian, Wenying Jiao, Yang |
author_facet | Zhang, Wenjia An, Fangmei Xia, Min Zhan, Qiang Tian, Wenying Jiao, Yang |
author_sort | Zhang, Wenjia |
collection | PubMed |
description | The aim of this study was to investigate the relationship between high-mobility group box 1 (HMGB1) and colorectal cancer (CRC). In this prospective study, patients with CRC undergoing primary surgery and healthy subjects (control group) were enrolled from July 2013 to December 2014. The serum HMGB1 concentration and HMGB1 mRNA expression were determined using enzyme-linked immunosorbent assay reverse transcription-polymerase chain reaction, respectively. Immunohistochemical analysis was performed to determine HMGB1, pERK, and c-inhibitor of apoptosis protein 2 (c-IAP2) protein expression levels in the cancer tissues. A total 144 patients with CRC and 50 healthy subjects underwent serum HMGB1 testing. Resected specimens of 50 patients were used for HMGB1 mRNA and protein expression analyses. Mean serum HMGB1 level in the patients with CRC was higher than that of the control group (8.42 μg/L vs 1.79 μg/L, P < .05). Mean serum HMGB1 level in the patients with CRC with distant metastasis was significantly higher than that of the controls (13.32 μg/L vs 7.37 μg/L, P < .05). The HMGB1 mRNA and protein expression levels in the CRC tissues were significantly higher than those in the adjacent normal mucosa. HMGB1 protein expression positively correlated with the lymph node metastasis. There were positive correlations between HMGB1 and c-IAP2 (r = 0.457, P < .05), HMGB1 and pERK (r = 0.461, P < .05), as well as pERK and c-IAP2 (r = 0.399, P < .05). HMGB1 expression in CRC correlates with distant and lymph node metastasis. It may inhibit apoptosis by inducing activation of pERK and c-IAP2. |
format | Online Article Text |
id | pubmed-6370169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-63701692019-02-22 Increased HMGB1 expression correlates with higher expression of c-IAP2 and pERK in colorectal cancer Zhang, Wenjia An, Fangmei Xia, Min Zhan, Qiang Tian, Wenying Jiao, Yang Medicine (Baltimore) Research Article The aim of this study was to investigate the relationship between high-mobility group box 1 (HMGB1) and colorectal cancer (CRC). In this prospective study, patients with CRC undergoing primary surgery and healthy subjects (control group) were enrolled from July 2013 to December 2014. The serum HMGB1 concentration and HMGB1 mRNA expression were determined using enzyme-linked immunosorbent assay reverse transcription-polymerase chain reaction, respectively. Immunohistochemical analysis was performed to determine HMGB1, pERK, and c-inhibitor of apoptosis protein 2 (c-IAP2) protein expression levels in the cancer tissues. A total 144 patients with CRC and 50 healthy subjects underwent serum HMGB1 testing. Resected specimens of 50 patients were used for HMGB1 mRNA and protein expression analyses. Mean serum HMGB1 level in the patients with CRC was higher than that of the control group (8.42 μg/L vs 1.79 μg/L, P < .05). Mean serum HMGB1 level in the patients with CRC with distant metastasis was significantly higher than that of the controls (13.32 μg/L vs 7.37 μg/L, P < .05). The HMGB1 mRNA and protein expression levels in the CRC tissues were significantly higher than those in the adjacent normal mucosa. HMGB1 protein expression positively correlated with the lymph node metastasis. There were positive correlations between HMGB1 and c-IAP2 (r = 0.457, P < .05), HMGB1 and pERK (r = 0.461, P < .05), as well as pERK and c-IAP2 (r = 0.399, P < .05). HMGB1 expression in CRC correlates with distant and lymph node metastasis. It may inhibit apoptosis by inducing activation of pERK and c-IAP2. Wolters Kluwer Health 2019-01-18 /pmc/articles/PMC6370169/ /pubmed/30653121 http://dx.doi.org/10.1097/MD.0000000000014069 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | Research Article Zhang, Wenjia An, Fangmei Xia, Min Zhan, Qiang Tian, Wenying Jiao, Yang Increased HMGB1 expression correlates with higher expression of c-IAP2 and pERK in colorectal cancer |
title | Increased HMGB1 expression correlates with higher expression of c-IAP2 and pERK in colorectal cancer |
title_full | Increased HMGB1 expression correlates with higher expression of c-IAP2 and pERK in colorectal cancer |
title_fullStr | Increased HMGB1 expression correlates with higher expression of c-IAP2 and pERK in colorectal cancer |
title_full_unstemmed | Increased HMGB1 expression correlates with higher expression of c-IAP2 and pERK in colorectal cancer |
title_short | Increased HMGB1 expression correlates with higher expression of c-IAP2 and pERK in colorectal cancer |
title_sort | increased hmgb1 expression correlates with higher expression of c-iap2 and perk in colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370169/ https://www.ncbi.nlm.nih.gov/pubmed/30653121 http://dx.doi.org/10.1097/MD.0000000000014069 |
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