Cargando…

High NANOG expression correlates with worse patients’ survival in esophageal adenocarcinoma

BACKGROUND: Patients diagnosed with esophageal cancer demonstrate a low overall survival even despite the established multimodal therapy as the current standard of care. Therefore, further biomarkers for patients with high-risk and additional therapy options are needed. NANOG is a transcription fact...

Descripción completa

Detalles Bibliográficos
Autores principales: Knipper, Karl, Damanakis, Alexander I., Lyu, Su Ir, Simon, Adrian Georg, Wahler, Isabell, Bruns, Christiane J., Schröder, Wolfgang, Schmidt, Thomas, Quaas, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351130/
https://www.ncbi.nlm.nih.gov/pubmed/37461005
http://dx.doi.org/10.1186/s12885-023-11146-0
_version_ 1785074280010088448
author Knipper, Karl
Damanakis, Alexander I.
Lyu, Su Ir
Simon, Adrian Georg
Wahler, Isabell
Bruns, Christiane J.
Schröder, Wolfgang
Schmidt, Thomas
Quaas, Alexander
author_facet Knipper, Karl
Damanakis, Alexander I.
Lyu, Su Ir
Simon, Adrian Georg
Wahler, Isabell
Bruns, Christiane J.
Schröder, Wolfgang
Schmidt, Thomas
Quaas, Alexander
author_sort Knipper, Karl
collection PubMed
description BACKGROUND: Patients diagnosed with esophageal cancer demonstrate a low overall survival even despite the established multimodal therapy as the current standard of care. Therefore, further biomarkers for patients with high-risk and additional therapy options are needed. NANOG is a transcription factor, which can be found in stem cells and is known to support tumorigenesis. METHODS: Six hundred sixty patients with esophageal adenocarcinoma, who were operated at the University of Cologne with a curative intent, were included. Immunohistochemical stainings for NANOG were performed. The study population was divided into NANOG-positive and -negative subgroups. RESULTS: Positive NANOG expression correlates significantly with worse overall survival (p = 0.002) and could be confirmed as an independent risk factor for worse patient survival in multivariate analysis (HR = 1.40, 95%CI = 1.09–1.80, p = 0.006). This effect could be detected in the subgroup of primarily operated patients, but not in patients after neoadjuvant therapy. CONCLUSIONS: We describe a NANOG-positive subgroup of patients with esophageal cancer, who exhibit worse overall survival in a large patient cohort. This discovery suggests the potential use of NANOG as a biomarker for both intensified therapy and stricter follow-up regimes. Additionally, NANOG-positive stem cell-like cancer cells could be used as a new antitumoral treatment target if validated in mechanistic and clinical studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11146-0.
format Online
Article
Text
id pubmed-10351130
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-103511302023-07-18 High NANOG expression correlates with worse patients’ survival in esophageal adenocarcinoma Knipper, Karl Damanakis, Alexander I. Lyu, Su Ir Simon, Adrian Georg Wahler, Isabell Bruns, Christiane J. Schröder, Wolfgang Schmidt, Thomas Quaas, Alexander BMC Cancer Research BACKGROUND: Patients diagnosed with esophageal cancer demonstrate a low overall survival even despite the established multimodal therapy as the current standard of care. Therefore, further biomarkers for patients with high-risk and additional therapy options are needed. NANOG is a transcription factor, which can be found in stem cells and is known to support tumorigenesis. METHODS: Six hundred sixty patients with esophageal adenocarcinoma, who were operated at the University of Cologne with a curative intent, were included. Immunohistochemical stainings for NANOG were performed. The study population was divided into NANOG-positive and -negative subgroups. RESULTS: Positive NANOG expression correlates significantly with worse overall survival (p = 0.002) and could be confirmed as an independent risk factor for worse patient survival in multivariate analysis (HR = 1.40, 95%CI = 1.09–1.80, p = 0.006). This effect could be detected in the subgroup of primarily operated patients, but not in patients after neoadjuvant therapy. CONCLUSIONS: We describe a NANOG-positive subgroup of patients with esophageal cancer, who exhibit worse overall survival in a large patient cohort. This discovery suggests the potential use of NANOG as a biomarker for both intensified therapy and stricter follow-up regimes. Additionally, NANOG-positive stem cell-like cancer cells could be used as a new antitumoral treatment target if validated in mechanistic and clinical studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11146-0. BioMed Central 2023-07-17 /pmc/articles/PMC10351130/ /pubmed/37461005 http://dx.doi.org/10.1186/s12885-023-11146-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Knipper, Karl
Damanakis, Alexander I.
Lyu, Su Ir
Simon, Adrian Georg
Wahler, Isabell
Bruns, Christiane J.
Schröder, Wolfgang
Schmidt, Thomas
Quaas, Alexander
High NANOG expression correlates with worse patients’ survival in esophageal adenocarcinoma
title High NANOG expression correlates with worse patients’ survival in esophageal adenocarcinoma
title_full High NANOG expression correlates with worse patients’ survival in esophageal adenocarcinoma
title_fullStr High NANOG expression correlates with worse patients’ survival in esophageal adenocarcinoma
title_full_unstemmed High NANOG expression correlates with worse patients’ survival in esophageal adenocarcinoma
title_short High NANOG expression correlates with worse patients’ survival in esophageal adenocarcinoma
title_sort high nanog expression correlates with worse patients’ survival in esophageal adenocarcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351130/
https://www.ncbi.nlm.nih.gov/pubmed/37461005
http://dx.doi.org/10.1186/s12885-023-11146-0
work_keys_str_mv AT knipperkarl highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma
AT damanakisalexanderi highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma
AT lyusuir highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma
AT simonadriangeorg highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma
AT wahlerisabell highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma
AT brunschristianej highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma
AT schroderwolfgang highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma
AT schmidtthomas highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma
AT quaasalexander highnanogexpressioncorrelateswithworsepatientssurvivalinesophagealadenocarcinoma