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P53 expression, DNA ploidy and S-phase cell fraction in operable locally advanced non-small-cell lung cancer.
The identification of biomarkers to complement pathological stage for a more accurate prognosis and help clinicians decide on treatment is still an open problem for patients with lung cancer. Expression of P53 protein was detected by an immunohistochemical approach using the monoclonal antibody PAb1...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074267/ https://www.ncbi.nlm.nih.gov/pubmed/8611406 |
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author | Costa, A. Silvestrini, R. Mochen, C. Lequaglie, C. Boracchi, P. Faranda, A. Vessecchia, G. Ravasi, G. |
author_facet | Costa, A. Silvestrini, R. Mochen, C. Lequaglie, C. Boracchi, P. Faranda, A. Vessecchia, G. Ravasi, G. |
author_sort | Costa, A. |
collection | PubMed |
description | The identification of biomarkers to complement pathological stage for a more accurate prognosis and help clinicians decide on treatment is still an open problem for patients with lung cancer. Expression of P53 protein was detected by an immunohistochemical approach using the monoclonal antibody PAb1801 on paraffin-embedded sections of tumours obtained surgically from 102 stage II - IIIa patients with non-small-cell lung cancer (52 squamous cell carcinomas, 50 adenocarcinomas). [3H]Thymidine labelling index, an indicator of the S-phase cell fraction, was evaluated on histological sections of [3H]thymidine-labelled tumour samples. DNA ploidy was defined by flow cytometric analysis on frozen tumour tissue. The biomarkers, histology and pathological stage were analysed in relation to relapse-free survival in univariate and multivariate analyses. Stage and interaction between [3H]thymidine labelling index and histology provided significant prognostic information for the overall series. [3H]thymidine labelling index was an independent prognostic indicator of 3 year relapse-free survival in patients with adenocarcinoma. The results indicate the importance of cell proliferation to complement prognostic information provided by pathological stage in patients with stage II-IIIa adenocarcinomas. |
format | Text |
id | pubmed-2074267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20742672009-09-10 P53 expression, DNA ploidy and S-phase cell fraction in operable locally advanced non-small-cell lung cancer. Costa, A. Silvestrini, R. Mochen, C. Lequaglie, C. Boracchi, P. Faranda, A. Vessecchia, G. Ravasi, G. Br J Cancer Research Article The identification of biomarkers to complement pathological stage for a more accurate prognosis and help clinicians decide on treatment is still an open problem for patients with lung cancer. Expression of P53 protein was detected by an immunohistochemical approach using the monoclonal antibody PAb1801 on paraffin-embedded sections of tumours obtained surgically from 102 stage II - IIIa patients with non-small-cell lung cancer (52 squamous cell carcinomas, 50 adenocarcinomas). [3H]Thymidine labelling index, an indicator of the S-phase cell fraction, was evaluated on histological sections of [3H]thymidine-labelled tumour samples. DNA ploidy was defined by flow cytometric analysis on frozen tumour tissue. The biomarkers, histology and pathological stage were analysed in relation to relapse-free survival in univariate and multivariate analyses. Stage and interaction between [3H]thymidine labelling index and histology provided significant prognostic information for the overall series. [3H]thymidine labelling index was an independent prognostic indicator of 3 year relapse-free survival in patients with adenocarcinoma. The results indicate the importance of cell proliferation to complement prognostic information provided by pathological stage in patients with stage II-IIIa adenocarcinomas. Nature Publishing Group 1996-04 /pmc/articles/PMC2074267/ /pubmed/8611406 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 Costa, A. Silvestrini, R. Mochen, C. Lequaglie, C. Boracchi, P. Faranda, A. Vessecchia, G. Ravasi, G. P53 expression, DNA ploidy and S-phase cell fraction in operable locally advanced non-small-cell lung cancer. |
title | P53 expression, DNA ploidy and S-phase cell fraction in operable locally advanced non-small-cell lung cancer. |
title_full | P53 expression, DNA ploidy and S-phase cell fraction in operable locally advanced non-small-cell lung cancer. |
title_fullStr | P53 expression, DNA ploidy and S-phase cell fraction in operable locally advanced non-small-cell lung cancer. |
title_full_unstemmed | P53 expression, DNA ploidy and S-phase cell fraction in operable locally advanced non-small-cell lung cancer. |
title_short | P53 expression, DNA ploidy and S-phase cell fraction in operable locally advanced non-small-cell lung cancer. |
title_sort | p53 expression, dna ploidy and s-phase cell fraction in operable locally advanced non-small-cell lung cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074267/ https://www.ncbi.nlm.nih.gov/pubmed/8611406 |
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