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Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma
Integrins are a large family of cell surface receptors that bind extracellular matrix proteins and participate in cancer progression. However, the prognostic value of integrin family genes in post-operative patients with HBV-related hepatocellular carcinoma (HCC) remains unknown. In this study, we i...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652745/ https://www.ncbi.nlm.nih.gov/pubmed/29100351 http://dx.doi.org/10.18632/oncotarget.20161 |
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author | Shang, Liming Ye, Xinping Zhu, Guangzhi Su, Hao Su, Zhixiong Chen, Bin Xiao, Kaiyin Li, Lequn Peng, Minhao Peng, Tao |
author_facet | Shang, Liming Ye, Xinping Zhu, Guangzhi Su, Hao Su, Zhixiong Chen, Bin Xiao, Kaiyin Li, Lequn Peng, Minhao Peng, Tao |
author_sort | Shang, Liming |
collection | PubMed |
description | Integrins are a large family of cell surface receptors that bind extracellular matrix proteins and participate in cancer progression. However, the prognostic value of integrin family genes in post-operative patients with HBV-related hepatocellular carcinoma (HCC) remains unknown. In this study, we investigated 18 single nucleotide polymorphisms (SNPs) in integrin family genes and found that the AG/GG genotypes at rs988574 in ITGA1 predicted a better prognosis compared to carriers of the AA genotype (P = 0.025, HR = 0.69, 95%CI = 0.50–0.96). Moreover, rs988574 genotype combined with serum level of AFP had a better prognostic value in HBV-related HCC patients (P = 0.026, HR = 1.75, 95% CI = 1.07–2.85). Furthermore, we compared the expression of 24 integrin family genes in HBV-related HCC tissues and adjacent normal tissues. Survival analysis demonstrated that expression of three of the family members, ITGA5, ITGB5 and ITGA2B, were significantly associated with the overall survival (OS) or relapse-free survival (RFS) of HBV-related HCC patients. Additionally, patients with lower expression of both ITGA5 and ITGB5 had the best OS and RFS (P = 0.017 and P = 0.002, respectively). Our study demonstrated that rs988574 of ITGA1 and the expression of ITGA5, ITGB5 and ITGA2B are potential independent prognostic bio-markers and therapeutic targets for HBV-related HCC patients and may be useful for the diagnosis of HBV-related HCC. |
format | Online Article Text |
id | pubmed-5652745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56527452017-11-02 Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma Shang, Liming Ye, Xinping Zhu, Guangzhi Su, Hao Su, Zhixiong Chen, Bin Xiao, Kaiyin Li, Lequn Peng, Minhao Peng, Tao Oncotarget Research Paper Integrins are a large family of cell surface receptors that bind extracellular matrix proteins and participate in cancer progression. However, the prognostic value of integrin family genes in post-operative patients with HBV-related hepatocellular carcinoma (HCC) remains unknown. In this study, we investigated 18 single nucleotide polymorphisms (SNPs) in integrin family genes and found that the AG/GG genotypes at rs988574 in ITGA1 predicted a better prognosis compared to carriers of the AA genotype (P = 0.025, HR = 0.69, 95%CI = 0.50–0.96). Moreover, rs988574 genotype combined with serum level of AFP had a better prognostic value in HBV-related HCC patients (P = 0.026, HR = 1.75, 95% CI = 1.07–2.85). Furthermore, we compared the expression of 24 integrin family genes in HBV-related HCC tissues and adjacent normal tissues. Survival analysis demonstrated that expression of three of the family members, ITGA5, ITGB5 and ITGA2B, were significantly associated with the overall survival (OS) or relapse-free survival (RFS) of HBV-related HCC patients. Additionally, patients with lower expression of both ITGA5 and ITGB5 had the best OS and RFS (P = 0.017 and P = 0.002, respectively). Our study demonstrated that rs988574 of ITGA1 and the expression of ITGA5, ITGB5 and ITGA2B are potential independent prognostic bio-markers and therapeutic targets for HBV-related HCC patients and may be useful for the diagnosis of HBV-related HCC. Impact Journals LLC 2017-08-10 /pmc/articles/PMC5652745/ /pubmed/29100351 http://dx.doi.org/10.18632/oncotarget.20161 Text en Copyright: © 2017 Shang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Shang, Liming Ye, Xinping Zhu, Guangzhi Su, Hao Su, Zhixiong Chen, Bin Xiao, Kaiyin Li, Lequn Peng, Minhao Peng, Tao Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma |
title | Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma |
title_full | Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma |
title_fullStr | Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma |
title_full_unstemmed | Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma |
title_short | Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma |
title_sort | prognostic value of integrin variants and expression in post-operative patients with hbv-related hepatocellular carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5652745/ https://www.ncbi.nlm.nih.gov/pubmed/29100351 http://dx.doi.org/10.18632/oncotarget.20161 |
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