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Notch Signaling Pathway in Pancreatobiliary Tumors

Background and Objectives: The Notch signaling pathway plays an important role both in the development of the ductal systems of the pancreas and the bile ducts as well as in cancer development and progression. The aim of this study was to examine the expression of central proteins of the Notch signa...

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Autores principales: Borlak, Francesca, Reutzel-Selke, Anja, Schirmeier, Anja, Gogolok, Julia, von Hoerschelmann, Ellen, Sauer, Igor M., Pratschke, Johann, Bahra, Marcus, Schmuck, Rosa B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911049/
https://www.ncbi.nlm.nih.gov/pubmed/33498866
http://dx.doi.org/10.3390/medicina57020105
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author Borlak, Francesca
Reutzel-Selke, Anja
Schirmeier, Anja
Gogolok, Julia
von Hoerschelmann, Ellen
Sauer, Igor M.
Pratschke, Johann
Bahra, Marcus
Schmuck, Rosa B.
author_facet Borlak, Francesca
Reutzel-Selke, Anja
Schirmeier, Anja
Gogolok, Julia
von Hoerschelmann, Ellen
Sauer, Igor M.
Pratschke, Johann
Bahra, Marcus
Schmuck, Rosa B.
author_sort Borlak, Francesca
collection PubMed
description Background and Objectives: The Notch signaling pathway plays an important role both in the development of the ductal systems of the pancreas and the bile ducts as well as in cancer development and progression. The aim of this study was to examine the expression of central proteins of the Notch signaling pathway in pancreatobiliary tumors and its influence on patient survival. Materials and Methods: We compared the receptors (Notch1, Notch4), activating splicing factors (ADAM17), and target genes (HES1) of the Notch pathway and progenitor cell markers with relevance for the Notch signaling pathway (CD44, MSI1) between pancreatic adenocarcinomas (PDAC, n = 14), intrahepatic cholangiocarcinoma (iCC, n = 24), and extrahepatic cholangiocarcinoma (eCC, n = 22) cholangiocarcinomas via immunohistochemistry and ImageJ software-assisted analysis. An Immunohistochemistry (IHC)-score was determined by the percentage and intensity of stained (positive) cells (scale 0–7) and normal and malignant tissue was compared. In the IHC results, patients’ (gender, age) and tumor (TNM Classification of Malignant Tumors, Union Internationale contre le Cancer (UICC) stages, grading, and lymphangitic carcinomatosa) characteristics were correlated to patient survival. Results: For eCC, the expression of CD44 (p = 0.043, IHC-score 3.94 vs. 3.54) and for iCC, the expression of CD44 (p = 0.026, IHC-score 4.04 vs. 3.48) and Notch1 (p < 0.001, IHC-score 2.87 vs. 1.78) was significantly higher in the tumor compared to non-malignant tissue. For PDAC, the expression of ADAM17 (p = 0.008, IHC-score 3.43 vs. 1.73), CD44 (p = 0.012, IHC-score 3.64 vs. 2.27), Notch1 (p = 0.012, IHC-score 2.21 vs. 0.64), and Notch4 (p = 0.008, IHC-score 2.86 vs. 0.91) was significantly higher in the tumor tissue. However, none of the analyzed Notch-signaling related components showed an association to patient survival. Conclusion: A significant overexpression of almost all studied components of the Notch signaling pathway can be found in the tumor tissue, however, without a significant influence on patient survival. Therefore, further studies are warranted to draw conclusions on Notch pathway’s relevance for patient survival.
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spelling pubmed-79110492021-02-28 Notch Signaling Pathway in Pancreatobiliary Tumors Borlak, Francesca Reutzel-Selke, Anja Schirmeier, Anja Gogolok, Julia von Hoerschelmann, Ellen Sauer, Igor M. Pratschke, Johann Bahra, Marcus Schmuck, Rosa B. Medicina (Kaunas) Article Background and Objectives: The Notch signaling pathway plays an important role both in the development of the ductal systems of the pancreas and the bile ducts as well as in cancer development and progression. The aim of this study was to examine the expression of central proteins of the Notch signaling pathway in pancreatobiliary tumors and its influence on patient survival. Materials and Methods: We compared the receptors (Notch1, Notch4), activating splicing factors (ADAM17), and target genes (HES1) of the Notch pathway and progenitor cell markers with relevance for the Notch signaling pathway (CD44, MSI1) between pancreatic adenocarcinomas (PDAC, n = 14), intrahepatic cholangiocarcinoma (iCC, n = 24), and extrahepatic cholangiocarcinoma (eCC, n = 22) cholangiocarcinomas via immunohistochemistry and ImageJ software-assisted analysis. An Immunohistochemistry (IHC)-score was determined by the percentage and intensity of stained (positive) cells (scale 0–7) and normal and malignant tissue was compared. In the IHC results, patients’ (gender, age) and tumor (TNM Classification of Malignant Tumors, Union Internationale contre le Cancer (UICC) stages, grading, and lymphangitic carcinomatosa) characteristics were correlated to patient survival. Results: For eCC, the expression of CD44 (p = 0.043, IHC-score 3.94 vs. 3.54) and for iCC, the expression of CD44 (p = 0.026, IHC-score 4.04 vs. 3.48) and Notch1 (p < 0.001, IHC-score 2.87 vs. 1.78) was significantly higher in the tumor compared to non-malignant tissue. For PDAC, the expression of ADAM17 (p = 0.008, IHC-score 3.43 vs. 1.73), CD44 (p = 0.012, IHC-score 3.64 vs. 2.27), Notch1 (p = 0.012, IHC-score 2.21 vs. 0.64), and Notch4 (p = 0.008, IHC-score 2.86 vs. 0.91) was significantly higher in the tumor tissue. However, none of the analyzed Notch-signaling related components showed an association to patient survival. Conclusion: A significant overexpression of almost all studied components of the Notch signaling pathway can be found in the tumor tissue, however, without a significant influence on patient survival. Therefore, further studies are warranted to draw conclusions on Notch pathway’s relevance for patient survival. MDPI 2021-01-24 /pmc/articles/PMC7911049/ /pubmed/33498866 http://dx.doi.org/10.3390/medicina57020105 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Borlak, Francesca
Reutzel-Selke, Anja
Schirmeier, Anja
Gogolok, Julia
von Hoerschelmann, Ellen
Sauer, Igor M.
Pratschke, Johann
Bahra, Marcus
Schmuck, Rosa B.
Notch Signaling Pathway in Pancreatobiliary Tumors
title Notch Signaling Pathway in Pancreatobiliary Tumors
title_full Notch Signaling Pathway in Pancreatobiliary Tumors
title_fullStr Notch Signaling Pathway in Pancreatobiliary Tumors
title_full_unstemmed Notch Signaling Pathway in Pancreatobiliary Tumors
title_short Notch Signaling Pathway in Pancreatobiliary Tumors
title_sort notch signaling pathway in pancreatobiliary tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911049/
https://www.ncbi.nlm.nih.gov/pubmed/33498866
http://dx.doi.org/10.3390/medicina57020105
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