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Complement activation in astrocytomas: deposition of C4d and patient outcome
BACKGROUND: C4d is a cleavage product of complement component C4 and is considered to serve as a marker for the site of complement activation. In this study C4d staining of grade I-IV astrocytic tumors was studied to explore if there is an association between complement activation and the grade of t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517746/ https://www.ncbi.nlm.nih.gov/pubmed/23199209 http://dx.doi.org/10.1186/1471-2407-12-565 |
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author | Mäkelä, Katri Helén, Pauli Haapasalo, Hannu Paavonen, Timo |
author_facet | Mäkelä, Katri Helén, Pauli Haapasalo, Hannu Paavonen, Timo |
author_sort | Mäkelä, Katri |
collection | PubMed |
description | BACKGROUND: C4d is a cleavage product of complement component C4 and is considered to serve as a marker for the site of complement activation. In this study C4d staining of grade I-IV astrocytic tumors was studied to explore if there is an association between complement activation and the grade of tumor, or patient survival. METHODS: Tissue micro-array samples of 102 astrocytomas were stained immunohistochemically. The material consisted of 9 pilocytic astrocytomas and 93 grade II-IV astrocytomas, of which 67 were primary resections and 26 recurrent tumors. The intensity of C4d staining as well as extent of C4d and CD34 staining were evaluated. The intensity of C4d staining was scored semiquantitatively. The extent of the staining was counted morphometrically with a point counting grid yielding a percent of C4d and CD34 positive area of the sample. RESULTS: The intensity and extent of C4d staining increased in grade II-IV diffusely infiltrating astrocytoma tumors in line with the malignancy grade (p = 0.034 and p = 0.016, respectively, Kruskal-Wallis test). However, C4d positive tumor area percentages were higher in grade I pilocytic astrocytomas than in grade II-IV diffusely infiltrating astrocytomas (p = 0.041, Mann–Whitney test). There was a significant correlation between CD34 positive and C4d positive endothelial area fraction in diffusely infiltrating astrocytomas (p < 0.001, Pearson correlation). In these tumors, the increasing intensity of C4d staining was also associated with worsened patient outcome (p = 0.014, log-rank test). CONCLUSION: The worsening of patient outcome and malignant progression of tumor cells seem to be connected to microenvironmental changes evoked by chronically activated complement. |
format | Online Article Text |
id | pubmed-3517746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35177462012-12-09 Complement activation in astrocytomas: deposition of C4d and patient outcome Mäkelä, Katri Helén, Pauli Haapasalo, Hannu Paavonen, Timo BMC Cancer Research Article BACKGROUND: C4d is a cleavage product of complement component C4 and is considered to serve as a marker for the site of complement activation. In this study C4d staining of grade I-IV astrocytic tumors was studied to explore if there is an association between complement activation and the grade of tumor, or patient survival. METHODS: Tissue micro-array samples of 102 astrocytomas were stained immunohistochemically. The material consisted of 9 pilocytic astrocytomas and 93 grade II-IV astrocytomas, of which 67 were primary resections and 26 recurrent tumors. The intensity of C4d staining as well as extent of C4d and CD34 staining were evaluated. The intensity of C4d staining was scored semiquantitatively. The extent of the staining was counted morphometrically with a point counting grid yielding a percent of C4d and CD34 positive area of the sample. RESULTS: The intensity and extent of C4d staining increased in grade II-IV diffusely infiltrating astrocytoma tumors in line with the malignancy grade (p = 0.034 and p = 0.016, respectively, Kruskal-Wallis test). However, C4d positive tumor area percentages were higher in grade I pilocytic astrocytomas than in grade II-IV diffusely infiltrating astrocytomas (p = 0.041, Mann–Whitney test). There was a significant correlation between CD34 positive and C4d positive endothelial area fraction in diffusely infiltrating astrocytomas (p < 0.001, Pearson correlation). In these tumors, the increasing intensity of C4d staining was also associated with worsened patient outcome (p = 0.014, log-rank test). CONCLUSION: The worsening of patient outcome and malignant progression of tumor cells seem to be connected to microenvironmental changes evoked by chronically activated complement. BioMed Central 2012-12-01 /pmc/articles/PMC3517746/ /pubmed/23199209 http://dx.doi.org/10.1186/1471-2407-12-565 Text en Copyright ©2012 Mäkelä 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 Mäkelä, Katri Helén, Pauli Haapasalo, Hannu Paavonen, Timo Complement activation in astrocytomas: deposition of C4d and patient outcome |
title | Complement activation in astrocytomas: deposition of C4d and patient outcome |
title_full | Complement activation in astrocytomas: deposition of C4d and patient outcome |
title_fullStr | Complement activation in astrocytomas: deposition of C4d and patient outcome |
title_full_unstemmed | Complement activation in astrocytomas: deposition of C4d and patient outcome |
title_short | Complement activation in astrocytomas: deposition of C4d and patient outcome |
title_sort | complement activation in astrocytomas: deposition of c4d and patient outcome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517746/ https://www.ncbi.nlm.nih.gov/pubmed/23199209 http://dx.doi.org/10.1186/1471-2407-12-565 |
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