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PTEN status in advanced colorectal cancer treated with cetuximab
BACKGROUND: Loss of phosphatase and tensin homologue deleted in chromosome 10 (PTEN) function in advanced colorectal cancer (CRC) may represent one of the resistance mechanisms to cetuximab by interfering with the epidermal growth factor receptor signal transduction pathway. METHODS: PTEN expression...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813733/ https://www.ncbi.nlm.nih.gov/pubmed/19953097 http://dx.doi.org/10.1038/sj.bjc.6605471 |
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author | Negri, F V Bozzetti, C Lagrasta, C A Crafa, P Bonasoni, M P Camisa, R Pedrazzi, G Ardizzoni, A |
author_facet | Negri, F V Bozzetti, C Lagrasta, C A Crafa, P Bonasoni, M P Camisa, R Pedrazzi, G Ardizzoni, A |
author_sort | Negri, F V |
collection | PubMed |
description | BACKGROUND: Loss of phosphatase and tensin homologue deleted in chromosome 10 (PTEN) function in advanced colorectal cancer (CRC) may represent one of the resistance mechanisms to cetuximab by interfering with the epidermal growth factor receptor signal transduction pathway. METHODS: PTEN expression tested by indirect immunofluorescence was evaluated both on primary (n=43) and on metastatic (n=24) sites in CRC patients treated with cetuximab. RESULTS: The loss of PTEN expression tested on metastatic sites was negatively associated with response (100% progressive disease (PD) in PTEN-negative cases vs 30% PD in PTEN-positive cases; P<0.05), PFS (0.8 vs 8.2 months; P<0.001) and OS (2.9 vs 14.2 months; P<0.001). CONCLUSION: A potential role of PTEN in the anti-tumour activity of cetuximab could be hypothesised. |
format | Text |
id | pubmed-2813733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-28137332011-01-05 PTEN status in advanced colorectal cancer treated with cetuximab Negri, F V Bozzetti, C Lagrasta, C A Crafa, P Bonasoni, M P Camisa, R Pedrazzi, G Ardizzoni, A Br J Cancer Short Communication BACKGROUND: Loss of phosphatase and tensin homologue deleted in chromosome 10 (PTEN) function in advanced colorectal cancer (CRC) may represent one of the resistance mechanisms to cetuximab by interfering with the epidermal growth factor receptor signal transduction pathway. METHODS: PTEN expression tested by indirect immunofluorescence was evaluated both on primary (n=43) and on metastatic (n=24) sites in CRC patients treated with cetuximab. RESULTS: The loss of PTEN expression tested on metastatic sites was negatively associated with response (100% progressive disease (PD) in PTEN-negative cases vs 30% PD in PTEN-positive cases; P<0.05), PFS (0.8 vs 8.2 months; P<0.001) and OS (2.9 vs 14.2 months; P<0.001). CONCLUSION: A potential role of PTEN in the anti-tumour activity of cetuximab could be hypothesised. Nature Publishing Group 2010-01-05 2009-12-01 /pmc/articles/PMC2813733/ /pubmed/19953097 http://dx.doi.org/10.1038/sj.bjc.6605471 Text en Copyright © 2010 Cancer Research UK 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 | Short Communication Negri, F V Bozzetti, C Lagrasta, C A Crafa, P Bonasoni, M P Camisa, R Pedrazzi, G Ardizzoni, A PTEN status in advanced colorectal cancer treated with cetuximab |
title | PTEN status in advanced colorectal cancer treated with cetuximab |
title_full | PTEN status in advanced colorectal cancer treated with cetuximab |
title_fullStr | PTEN status in advanced colorectal cancer treated with cetuximab |
title_full_unstemmed | PTEN status in advanced colorectal cancer treated with cetuximab |
title_short | PTEN status in advanced colorectal cancer treated with cetuximab |
title_sort | pten status in advanced colorectal cancer treated with cetuximab |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813733/ https://www.ncbi.nlm.nih.gov/pubmed/19953097 http://dx.doi.org/10.1038/sj.bjc.6605471 |
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