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TLR9 expression in glioma tissues correlated to glioma progression and the prognosis of GBM patients
BACKGROUND: Our study aims to evaluate the expression of TLR9 in glioma tissues, examine the association between TLR9 expression, clinicopathological variables, and glioma patient outcome, we further characterized the direct effects of TLR9 agonist CpG ODN upon the proliferation and invasion of glio...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924315/ https://www.ncbi.nlm.nih.gov/pubmed/20696081 http://dx.doi.org/10.1186/1471-2407-10-415 |
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author | Wang, Chao Cao, Shouqiang Yan, Ying Ying, Qiao Jiang, Tao Xu, Ke Wu, Anhua |
author_facet | Wang, Chao Cao, Shouqiang Yan, Ying Ying, Qiao Jiang, Tao Xu, Ke Wu, Anhua |
author_sort | Wang, Chao |
collection | PubMed |
description | BACKGROUND: Our study aims to evaluate the expression of TLR9 in glioma tissues, examine the association between TLR9 expression, clinicopathological variables, and glioma patient outcome, we further characterized the direct effects of TLR9 agonist CpG ODN upon the proliferation and invasion of glioma cells in vitro. METHODS: RT-PCR and immunofluorescence were used to determine the expression of TLR9 in glioma cell lines and clinical glioma samples. Tissue microarry and immunohistochemistry were applied to evaluated TLR9 expression in 292 newly diagnosed glioma and 13 non-neoplastic brain tissues. We further investigated the effect of CpG ODN on the proliferation and invasion of glioma cells in vitro with MTT assays and matrigel transwell assay respectively. RESULTS: RT-PCR showed that TLR9 expressed in all the glioma samples and glioma cell lines we examined. The tissue array analysis indicated that TLR9 expression is correlated with malignancy of glioma (p < 0.01). Multivariate Cox regression analysis revealed that TLR9 expression is an independent prognostic factor for PFS of GBM patients(P = 0.026). TLR9 agonist CpG ODN has no significant effect on glioma proliferation, but matrigel transwell analysis showed that TLR9 agonist CpG ODN can significantly enhance glioma invasion in vitro. CONCLUSIONS: Our data indicated that TLR9 expression increases according to the histopathological grade of glioma, and the TLR9 expression level is related to the PFS of GBM patients. In addition, our findings warrant caution in the directly injection of TLR9 agonist CpG ODN into glioma tissues for the glioma immunotherapy. |
format | Text |
id | pubmed-2924315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29243152010-08-20 TLR9 expression in glioma tissues correlated to glioma progression and the prognosis of GBM patients Wang, Chao Cao, Shouqiang Yan, Ying Ying, Qiao Jiang, Tao Xu, Ke Wu, Anhua BMC Cancer Research Article BACKGROUND: Our study aims to evaluate the expression of TLR9 in glioma tissues, examine the association between TLR9 expression, clinicopathological variables, and glioma patient outcome, we further characterized the direct effects of TLR9 agonist CpG ODN upon the proliferation and invasion of glioma cells in vitro. METHODS: RT-PCR and immunofluorescence were used to determine the expression of TLR9 in glioma cell lines and clinical glioma samples. Tissue microarry and immunohistochemistry were applied to evaluated TLR9 expression in 292 newly diagnosed glioma and 13 non-neoplastic brain tissues. We further investigated the effect of CpG ODN on the proliferation and invasion of glioma cells in vitro with MTT assays and matrigel transwell assay respectively. RESULTS: RT-PCR showed that TLR9 expressed in all the glioma samples and glioma cell lines we examined. The tissue array analysis indicated that TLR9 expression is correlated with malignancy of glioma (p < 0.01). Multivariate Cox regression analysis revealed that TLR9 expression is an independent prognostic factor for PFS of GBM patients(P = 0.026). TLR9 agonist CpG ODN has no significant effect on glioma proliferation, but matrigel transwell analysis showed that TLR9 agonist CpG ODN can significantly enhance glioma invasion in vitro. CONCLUSIONS: Our data indicated that TLR9 expression increases according to the histopathological grade of glioma, and the TLR9 expression level is related to the PFS of GBM patients. In addition, our findings warrant caution in the directly injection of TLR9 agonist CpG ODN into glioma tissues for the glioma immunotherapy. BioMed Central 2010-08-10 /pmc/articles/PMC2924315/ /pubmed/20696081 http://dx.doi.org/10.1186/1471-2407-10-415 Text en Copyright ©2010 Wang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Chao Cao, Shouqiang Yan, Ying Ying, Qiao Jiang, Tao Xu, Ke Wu, Anhua TLR9 expression in glioma tissues correlated to glioma progression and the prognosis of GBM patients |
title | TLR9 expression in glioma tissues correlated to glioma progression and the prognosis of GBM patients |
title_full | TLR9 expression in glioma tissues correlated to glioma progression and the prognosis of GBM patients |
title_fullStr | TLR9 expression in glioma tissues correlated to glioma progression and the prognosis of GBM patients |
title_full_unstemmed | TLR9 expression in glioma tissues correlated to glioma progression and the prognosis of GBM patients |
title_short | TLR9 expression in glioma tissues correlated to glioma progression and the prognosis of GBM patients |
title_sort | tlr9 expression in glioma tissues correlated to glioma progression and the prognosis of gbm patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924315/ https://www.ncbi.nlm.nih.gov/pubmed/20696081 http://dx.doi.org/10.1186/1471-2407-10-415 |
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