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Association of angiogenic factors with prognosis in esophageal cancer
BACKGROUND: Despite multimodal therapy esophageal cancer often presents with poor prognosis. To improve outcome, tumor angiogenesis and anti-angiogenic therapeutic agents have recently gained importance. However, patient subgroups who benefit from anti-angiogenic therapy are not yet defined. In this...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362831/ https://www.ncbi.nlm.nih.gov/pubmed/25885021 http://dx.doi.org/10.1186/s12885-015-1120-5 |
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author | Dreikhausen, Lena Blank, Susanne Sisic, Leila Heger, Ulrike Weichert, Wilko Jäger, Dirk Bruckner, Thomas Giese, Natalia Grenacher, Lars Falk, Christine Ott, Katja Schmidt, Thomas |
author_facet | Dreikhausen, Lena Blank, Susanne Sisic, Leila Heger, Ulrike Weichert, Wilko Jäger, Dirk Bruckner, Thomas Giese, Natalia Grenacher, Lars Falk, Christine Ott, Katja Schmidt, Thomas |
author_sort | Dreikhausen, Lena |
collection | PubMed |
description | BACKGROUND: Despite multimodal therapy esophageal cancer often presents with poor prognosis. To improve outcome, tumor angiogenesis and anti-angiogenic therapeutic agents have recently gained importance. However, patient subgroups who benefit from anti-angiogenic therapy are not yet defined. In this retrospective exploratory study we investigated 9 angiogenic factors in patients’ serum and tissue samples with regard to their association with clinicopathological parameters, prognosis and response in patients with locally advanced preoperatively treated esophageal cancer. METHODS: From 2007 to 2012 preoperative serum and corresponding tumor tissue (n = 54), only serum (n = 20) or only tumor tissue (n = 4) were collected from esophageal squamous cell carcinoma (SCC) (n = 34) and adenocarcinoma of the esophagogastric junction (AEG) (n = 44) staged cT3/4NanyM0/x after preoperative chemo(radio)therapy. Angiogenic cytokine levels in both tissue and serum were measured by multiplex immunoassay. RESULTS: Median survival in all patients was 28.49 months. No significant difference was found in survival between SCC and AEG (p = 0.90). 26 patients were histopathological responders. Histopathological response was associated with prognosis (p = 0.05). Angiogenic factors were associated with the following clinicopathological factors: tumor tissue expression of Angiopoietin-2 and Follistatin was higher in SCC compared to AEG (p = 0.022 and p = 0.001). High HGF and Follistatin expression in the tumor tissue was associated with poor prognosis in all patients (p = 0.037 and p = 0.036). No association with prognosis was found in the patients’ serum. Neither patients’ serum nor tumor tissue showed an association between angiogenic factors and response to neoadjuvant therapy. CONCLUSION: Two angiogenic factors (HGF and Follistatin) in posttherapeutic tumor tissue are associated with prognosis in esophageal cancer patients. Biological differences of AEG and SCC with respect to angiogenesis were evident by the different expression of 2 angiogenic factors. Results are promising and should be pursued prospectively, optimally sequentially pre- and posttherapeutically. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-015-1120-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4362831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43628312015-03-18 Association of angiogenic factors with prognosis in esophageal cancer Dreikhausen, Lena Blank, Susanne Sisic, Leila Heger, Ulrike Weichert, Wilko Jäger, Dirk Bruckner, Thomas Giese, Natalia Grenacher, Lars Falk, Christine Ott, Katja Schmidt, Thomas BMC Cancer Research Article BACKGROUND: Despite multimodal therapy esophageal cancer often presents with poor prognosis. To improve outcome, tumor angiogenesis and anti-angiogenic therapeutic agents have recently gained importance. However, patient subgroups who benefit from anti-angiogenic therapy are not yet defined. In this retrospective exploratory study we investigated 9 angiogenic factors in patients’ serum and tissue samples with regard to their association with clinicopathological parameters, prognosis and response in patients with locally advanced preoperatively treated esophageal cancer. METHODS: From 2007 to 2012 preoperative serum and corresponding tumor tissue (n = 54), only serum (n = 20) or only tumor tissue (n = 4) were collected from esophageal squamous cell carcinoma (SCC) (n = 34) and adenocarcinoma of the esophagogastric junction (AEG) (n = 44) staged cT3/4NanyM0/x after preoperative chemo(radio)therapy. Angiogenic cytokine levels in both tissue and serum were measured by multiplex immunoassay. RESULTS: Median survival in all patients was 28.49 months. No significant difference was found in survival between SCC and AEG (p = 0.90). 26 patients were histopathological responders. Histopathological response was associated with prognosis (p = 0.05). Angiogenic factors were associated with the following clinicopathological factors: tumor tissue expression of Angiopoietin-2 and Follistatin was higher in SCC compared to AEG (p = 0.022 and p = 0.001). High HGF and Follistatin expression in the tumor tissue was associated with poor prognosis in all patients (p = 0.037 and p = 0.036). No association with prognosis was found in the patients’ serum. Neither patients’ serum nor tumor tissue showed an association between angiogenic factors and response to neoadjuvant therapy. CONCLUSION: Two angiogenic factors (HGF and Follistatin) in posttherapeutic tumor tissue are associated with prognosis in esophageal cancer patients. Biological differences of AEG and SCC with respect to angiogenesis were evident by the different expression of 2 angiogenic factors. Results are promising and should be pursued prospectively, optimally sequentially pre- and posttherapeutically. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-015-1120-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-13 /pmc/articles/PMC4362831/ /pubmed/25885021 http://dx.doi.org/10.1186/s12885-015-1120-5 Text en © Dreikhausen et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Dreikhausen, Lena Blank, Susanne Sisic, Leila Heger, Ulrike Weichert, Wilko Jäger, Dirk Bruckner, Thomas Giese, Natalia Grenacher, Lars Falk, Christine Ott, Katja Schmidt, Thomas Association of angiogenic factors with prognosis in esophageal cancer |
title | Association of angiogenic factors with prognosis in esophageal cancer |
title_full | Association of angiogenic factors with prognosis in esophageal cancer |
title_fullStr | Association of angiogenic factors with prognosis in esophageal cancer |
title_full_unstemmed | Association of angiogenic factors with prognosis in esophageal cancer |
title_short | Association of angiogenic factors with prognosis in esophageal cancer |
title_sort | association of angiogenic factors with prognosis in esophageal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362831/ https://www.ncbi.nlm.nih.gov/pubmed/25885021 http://dx.doi.org/10.1186/s12885-015-1120-5 |
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