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p53 protein in low-grade astrocytomas: a study with long-term follow-up.
The immunohistochemical expression of p53 protein (p53) was examined in 52 patients out of a series of 66 patients with low-grade astrocytomas with long-term follow-up. All patients were also evaluated for several clinical and histological features, among which only preoperative Karnofsky score and...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1994
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968882/ https://www.ncbi.nlm.nih.gov/pubmed/8123492 |
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author | Iuzzolino, P. Ghimenton, C. Nicolato, A. Giorgiutti, F. Fina, P. Doglioni, C. Barbareschi, M. |
author_facet | Iuzzolino, P. Ghimenton, C. Nicolato, A. Giorgiutti, F. Fina, P. Doglioni, C. Barbareschi, M. |
author_sort | Iuzzolino, P. |
collection | PubMed |
description | The immunohistochemical expression of p53 protein (p53) was examined in 52 patients out of a series of 66 patients with low-grade astrocytomas with long-term follow-up. All patients were also evaluated for several clinical and histological features, among which only preoperative Karnofsky score and the extent of surgery were statistically significant parameters to predict outcome on multivariate analysis. p53 accumulation was seen in 46.1% of patients, with a wide range of percentage of positive cells. Median survival for p53-positive and p53-negative patients was 41 and 37 months respectively. The survival curves of p53-positive and -negative patients were not statistically different. However, the curves showed a trend towards a more aggressive course in p53-positive patients beginning 3-4 years after surgery. Five years after diagnosis the survival estimate with the Kaplan-Meier method was 21.2% for patients with p53-positive tumours and 45.9% for patients with p53-negative tumours. This trend is not due to different distribution of major clinical prognostic factors (age, incomplete resection or Karnofsky status). The trend could be related to the time needed by the p53-positive clone to outgrow the rest of the p53-negative neoplastic cell population. This hypothesis is further supported by the fact that the five recurrences which were surgically removed (one anaplastic astrocytoma and four glioblastomas) derived from p53-positive tumours and were themselves intensely p53 positive. IMAGES: |
format | Text |
id | pubmed-1968882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19688822009-09-10 p53 protein in low-grade astrocytomas: a study with long-term follow-up. Iuzzolino, P. Ghimenton, C. Nicolato, A. Giorgiutti, F. Fina, P. Doglioni, C. Barbareschi, M. Br J Cancer Research Article The immunohistochemical expression of p53 protein (p53) was examined in 52 patients out of a series of 66 patients with low-grade astrocytomas with long-term follow-up. All patients were also evaluated for several clinical and histological features, among which only preoperative Karnofsky score and the extent of surgery were statistically significant parameters to predict outcome on multivariate analysis. p53 accumulation was seen in 46.1% of patients, with a wide range of percentage of positive cells. Median survival for p53-positive and p53-negative patients was 41 and 37 months respectively. The survival curves of p53-positive and -negative patients were not statistically different. However, the curves showed a trend towards a more aggressive course in p53-positive patients beginning 3-4 years after surgery. Five years after diagnosis the survival estimate with the Kaplan-Meier method was 21.2% for patients with p53-positive tumours and 45.9% for patients with p53-negative tumours. This trend is not due to different distribution of major clinical prognostic factors (age, incomplete resection or Karnofsky status). The trend could be related to the time needed by the p53-positive clone to outgrow the rest of the p53-negative neoplastic cell population. This hypothesis is further supported by the fact that the five recurrences which were surgically removed (one anaplastic astrocytoma and four glioblastomas) derived from p53-positive tumours and were themselves intensely p53 positive. IMAGES: Nature Publishing Group 1994-03 /pmc/articles/PMC1968882/ /pubmed/8123492 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Iuzzolino, P. Ghimenton, C. Nicolato, A. Giorgiutti, F. Fina, P. Doglioni, C. Barbareschi, M. p53 protein in low-grade astrocytomas: a study with long-term follow-up. |
title | p53 protein in low-grade astrocytomas: a study with long-term follow-up. |
title_full | p53 protein in low-grade astrocytomas: a study with long-term follow-up. |
title_fullStr | p53 protein in low-grade astrocytomas: a study with long-term follow-up. |
title_full_unstemmed | p53 protein in low-grade astrocytomas: a study with long-term follow-up. |
title_short | p53 protein in low-grade astrocytomas: a study with long-term follow-up. |
title_sort | p53 protein in low-grade astrocytomas: a study with long-term follow-up. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968882/ https://www.ncbi.nlm.nih.gov/pubmed/8123492 |
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