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A Combined TLR7/TLR9/GATA3 Score Can Predict Prognosis in Biliary Tract Cancer

Biliary tract cancer (BTC) refers to a heterogenous group of epithelial malignancies arising along the biliary tree. The highly aggressive nature combined with its silent presentation contribute to the dismal prognosis of this tumor. Tumor-infiltrating immune cells (TIICs) are frequently present in...

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Autores principales: Branchi, Vittorio, Esser, Laura, Boden, Corinna, Jafari, Azin, Henn, Jonas, Lingohr, Philipp, Gonzalez-Carmona, Maria A., Schmitz, Marc, Weismüller, Tobias J., Strassburg, Christian P., Manekeller, Steffen, Kristiansen, Glen, Kalff, Jörg C., Matthaei, Hanno, Toma, Marieta I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469358/
https://www.ncbi.nlm.nih.gov/pubmed/34573939
http://dx.doi.org/10.3390/diagnostics11091597
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author Branchi, Vittorio
Esser, Laura
Boden, Corinna
Jafari, Azin
Henn, Jonas
Lingohr, Philipp
Gonzalez-Carmona, Maria A.
Schmitz, Marc
Weismüller, Tobias J.
Strassburg, Christian P.
Manekeller, Steffen
Kristiansen, Glen
Kalff, Jörg C.
Matthaei, Hanno
Toma, Marieta I.
author_facet Branchi, Vittorio
Esser, Laura
Boden, Corinna
Jafari, Azin
Henn, Jonas
Lingohr, Philipp
Gonzalez-Carmona, Maria A.
Schmitz, Marc
Weismüller, Tobias J.
Strassburg, Christian P.
Manekeller, Steffen
Kristiansen, Glen
Kalff, Jörg C.
Matthaei, Hanno
Toma, Marieta I.
author_sort Branchi, Vittorio
collection PubMed
description Biliary tract cancer (BTC) refers to a heterogenous group of epithelial malignancies arising along the biliary tree. The highly aggressive nature combined with its silent presentation contribute to the dismal prognosis of this tumor. Tumor-infiltrating immune cells (TIICs) are frequently present in BTC and there is growing evidence regarding their role as therapeutic targets. In this study, we analyzed the immune cell infiltration in BTC and developed a promising immune signature score to predict prognosis in BTC. Immunohistochemistry (IHC) was carried out on tissue microarray sections from 45 patients with resectable cholangiocarcinoma for the detection of 6-sulfoLacNAc+ monocytes (slanMo), BDCA-2+ plasmacytoid dendritic cells (pDC), CD8+ or CD4+T-lymphocytes, CD103+ cells, GATA3+ cells, Toll-like receptor (TLR) 3, 7 and 9-expressing cells as well as programmed cell death protein 1 and programmed cell death ligand 1 positive cells. Data from the IHC staining were analyzed and correlated with clinicopathological and survival data. High expression of TLR7, TLR9, and GATA3 was associated with improved overall survival (OS, Log-rank p < 0.05). In addition, TLR9 was associated with better disease-free survival (Log-rank p < 0.05). In the multivariate Cox proportional-hazards model for OS, the TLR/TLR9/GATA3 score was found to be an independent prognostic factor for OS (“Score 2” vs. “Score 0”: HR 11.17 95% CI 2.27–54.95, p < 0.01).
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spelling pubmed-84693582021-09-27 A Combined TLR7/TLR9/GATA3 Score Can Predict Prognosis in Biliary Tract Cancer Branchi, Vittorio Esser, Laura Boden, Corinna Jafari, Azin Henn, Jonas Lingohr, Philipp Gonzalez-Carmona, Maria A. Schmitz, Marc Weismüller, Tobias J. Strassburg, Christian P. Manekeller, Steffen Kristiansen, Glen Kalff, Jörg C. Matthaei, Hanno Toma, Marieta I. Diagnostics (Basel) Article Biliary tract cancer (BTC) refers to a heterogenous group of epithelial malignancies arising along the biliary tree. The highly aggressive nature combined with its silent presentation contribute to the dismal prognosis of this tumor. Tumor-infiltrating immune cells (TIICs) are frequently present in BTC and there is growing evidence regarding their role as therapeutic targets. In this study, we analyzed the immune cell infiltration in BTC and developed a promising immune signature score to predict prognosis in BTC. Immunohistochemistry (IHC) was carried out on tissue microarray sections from 45 patients with resectable cholangiocarcinoma for the detection of 6-sulfoLacNAc+ monocytes (slanMo), BDCA-2+ plasmacytoid dendritic cells (pDC), CD8+ or CD4+T-lymphocytes, CD103+ cells, GATA3+ cells, Toll-like receptor (TLR) 3, 7 and 9-expressing cells as well as programmed cell death protein 1 and programmed cell death ligand 1 positive cells. Data from the IHC staining were analyzed and correlated with clinicopathological and survival data. High expression of TLR7, TLR9, and GATA3 was associated with improved overall survival (OS, Log-rank p < 0.05). In addition, TLR9 was associated with better disease-free survival (Log-rank p < 0.05). In the multivariate Cox proportional-hazards model for OS, the TLR/TLR9/GATA3 score was found to be an independent prognostic factor for OS (“Score 2” vs. “Score 0”: HR 11.17 95% CI 2.27–54.95, p < 0.01). MDPI 2021-09-01 /pmc/articles/PMC8469358/ /pubmed/34573939 http://dx.doi.org/10.3390/diagnostics11091597 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Branchi, Vittorio
Esser, Laura
Boden, Corinna
Jafari, Azin
Henn, Jonas
Lingohr, Philipp
Gonzalez-Carmona, Maria A.
Schmitz, Marc
Weismüller, Tobias J.
Strassburg, Christian P.
Manekeller, Steffen
Kristiansen, Glen
Kalff, Jörg C.
Matthaei, Hanno
Toma, Marieta I.
A Combined TLR7/TLR9/GATA3 Score Can Predict Prognosis in Biliary Tract Cancer
title A Combined TLR7/TLR9/GATA3 Score Can Predict Prognosis in Biliary Tract Cancer
title_full A Combined TLR7/TLR9/GATA3 Score Can Predict Prognosis in Biliary Tract Cancer
title_fullStr A Combined TLR7/TLR9/GATA3 Score Can Predict Prognosis in Biliary Tract Cancer
title_full_unstemmed A Combined TLR7/TLR9/GATA3 Score Can Predict Prognosis in Biliary Tract Cancer
title_short A Combined TLR7/TLR9/GATA3 Score Can Predict Prognosis in Biliary Tract Cancer
title_sort combined tlr7/tlr9/gata3 score can predict prognosis in biliary tract cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469358/
https://www.ncbi.nlm.nih.gov/pubmed/34573939
http://dx.doi.org/10.3390/diagnostics11091597
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