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Impact of PINCH expression on survival in colorectal cancer patients
BACKGROUND: The adaptor protein PINCH is overexpressed in the stroma of several types of cancer, and is an independent prognostic marker in colorectal cancer. In this study we further investigate the relationship of PINCH and survival regarding the response to chemotherapy in colorectal cancer. RESU...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3071339/ https://www.ncbi.nlm.nih.gov/pubmed/21426571 http://dx.doi.org/10.1186/1471-2407-11-103 |
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author | Lööf, Jasmine Rosell, Johan Bratthäll, Charlotte Doré, Siv Starkhammar, Hans Zhang, Hong Sun, Xiao-Feng |
author_facet | Lööf, Jasmine Rosell, Johan Bratthäll, Charlotte Doré, Siv Starkhammar, Hans Zhang, Hong Sun, Xiao-Feng |
author_sort | Lööf, Jasmine |
collection | PubMed |
description | BACKGROUND: The adaptor protein PINCH is overexpressed in the stroma of several types of cancer, and is an independent prognostic marker in colorectal cancer. In this study we further investigate the relationship of PINCH and survival regarding the response to chemotherapy in colorectal cancer. RESULTS: Paraffin-embedded tissue sections from 251 primary adenocarcinomas, 149 samples of adjacent normal mucosa, 57 samples of distant normal mucosa and 75 lymph node metastases were used for immunohistochemical staining. Stromal staining for PINCH increased from normal mucosa to primary tumour to metastasis. Strong staining in adjacent normal mucosa was related to worse survival independently of sex, age, tumour location, differentiation and stage (p = 0.044, HR, 1.60, 95% CI, 1.01-2.52). PINCH staining at the invasive margin tended to be related to survival (p = 0.051). In poorly differentiated tumours PINCH staining at the invasive margin was related to survival independently of sex, age and stage (p = 0.013, HR, 1.90, 95% CI, 1.14-3.16), while in better differentiated tumours it was not. In patients with weak staining, adjuvant chemotherapy was related to survival (p = 0.010, 0.013 and 0.013 in entire tumour area, invasive margin and inner tumour area, respectively), but not in patients with strong staining. However, in the multivariate analysis no such relationship was seen. CONCLUSIONS: PINCH staining in normal adjacent mucosa was related to survival. Further, PINCH staining at the tumour invasive margin was related to survival in poorly differentiated tumours but not in better differentiated tumours, indicating that the impact of PINCH on prognosis was dependent on differentiation status. |
format | Text |
id | pubmed-3071339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30713392011-04-06 Impact of PINCH expression on survival in colorectal cancer patients Lööf, Jasmine Rosell, Johan Bratthäll, Charlotte Doré, Siv Starkhammar, Hans Zhang, Hong Sun, Xiao-Feng BMC Cancer Research Article BACKGROUND: The adaptor protein PINCH is overexpressed in the stroma of several types of cancer, and is an independent prognostic marker in colorectal cancer. In this study we further investigate the relationship of PINCH and survival regarding the response to chemotherapy in colorectal cancer. RESULTS: Paraffin-embedded tissue sections from 251 primary adenocarcinomas, 149 samples of adjacent normal mucosa, 57 samples of distant normal mucosa and 75 lymph node metastases were used for immunohistochemical staining. Stromal staining for PINCH increased from normal mucosa to primary tumour to metastasis. Strong staining in adjacent normal mucosa was related to worse survival independently of sex, age, tumour location, differentiation and stage (p = 0.044, HR, 1.60, 95% CI, 1.01-2.52). PINCH staining at the invasive margin tended to be related to survival (p = 0.051). In poorly differentiated tumours PINCH staining at the invasive margin was related to survival independently of sex, age and stage (p = 0.013, HR, 1.90, 95% CI, 1.14-3.16), while in better differentiated tumours it was not. In patients with weak staining, adjuvant chemotherapy was related to survival (p = 0.010, 0.013 and 0.013 in entire tumour area, invasive margin and inner tumour area, respectively), but not in patients with strong staining. However, in the multivariate analysis no such relationship was seen. CONCLUSIONS: PINCH staining in normal adjacent mucosa was related to survival. Further, PINCH staining at the tumour invasive margin was related to survival in poorly differentiated tumours but not in better differentiated tumours, indicating that the impact of PINCH on prognosis was dependent on differentiation status. BioMed Central 2011-03-22 /pmc/articles/PMC3071339/ /pubmed/21426571 http://dx.doi.org/10.1186/1471-2407-11-103 Text en Copyright ©2011 Lööf 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 Lööf, Jasmine Rosell, Johan Bratthäll, Charlotte Doré, Siv Starkhammar, Hans Zhang, Hong Sun, Xiao-Feng Impact of PINCH expression on survival in colorectal cancer patients |
title | Impact of PINCH expression on survival in colorectal cancer patients |
title_full | Impact of PINCH expression on survival in colorectal cancer patients |
title_fullStr | Impact of PINCH expression on survival in colorectal cancer patients |
title_full_unstemmed | Impact of PINCH expression on survival in colorectal cancer patients |
title_short | Impact of PINCH expression on survival in colorectal cancer patients |
title_sort | impact of pinch expression on survival in colorectal cancer patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3071339/ https://www.ncbi.nlm.nih.gov/pubmed/21426571 http://dx.doi.org/10.1186/1471-2407-11-103 |
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