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The Expression of Programmed Death-Ligand 1 on Immune Cells Is Related to a Better Prognosis in Biliary Tract Cancer

BACKGROUND/AIMS: Programmed death-ligand 1 (PD-L1) expression in tumor cells is associated with a poor biliary tract cancer (BTC) prognosis; tumor-infiltrating immune cells in the tumor microenvironment are associated with a better prognosis. The effect of PD-L1 expression on immune cells on surviva...

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Autores principales: Kwon, Sung Chan, Bang, Seungmin, Park, Young Nyun, Park, Ji Hoon, Kim, So Jeong, Jo, Jung Hyun, Chung, Moon Jae, Park, Jeong Youp, Park, Seung Woo, Song, Si Young, Park, Eunhyang, Lee, Hee Seung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651371/
https://www.ncbi.nlm.nih.gov/pubmed/36510775
http://dx.doi.org/10.5009/gnl220206
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author Kwon, Sung Chan
Bang, Seungmin
Park, Young Nyun
Park, Ji Hoon
Kim, So Jeong
Jo, Jung Hyun
Chung, Moon Jae
Park, Jeong Youp
Park, Seung Woo
Song, Si Young
Park, Eunhyang
Lee, Hee Seung
author_facet Kwon, Sung Chan
Bang, Seungmin
Park, Young Nyun
Park, Ji Hoon
Kim, So Jeong
Jo, Jung Hyun
Chung, Moon Jae
Park, Jeong Youp
Park, Seung Woo
Song, Si Young
Park, Eunhyang
Lee, Hee Seung
author_sort Kwon, Sung Chan
collection PubMed
description BACKGROUND/AIMS: Programmed death-ligand 1 (PD-L1) expression in tumor cells is associated with a poor biliary tract cancer (BTC) prognosis; tumor-infiltrating immune cells in the tumor microenvironment are associated with a better prognosis. The effect of PD-L1 expression on immune cells on survival is unclear. We investigated the relationship between PD-L1 expression in immune cells and BTC prognosis. METHODS: PD-L1 expression was evaluated using an anti-PD-L1 22C3 mouse monoclonal primary antibody, and its relationships with clinical characteristics and prognosis were analyzed using the Cox proportional hazard model to investigate the prognostic performance of PD-L1 in BTC. RESULTS: Among 144 analyzed cases, patients with positive PD-L1 expression in tumor cells and negative PD-L1 expression in immune cells showed poorer overall survival rates than those exhibiting other expressions (tumor cells hazard ratio [HR]=1.023, p<0.001; immune cells HR=0.983, p=0.021). PD-L1 expression in tumor cells was an independent predictor of poor overall survival (HR=1.024, p<0.001). In contrast, PD-L1 expression in immune cells was a predictive marker of good prognosis (HR=0.983, p=0.018). CONCLUSIONS: PD-L1 expression in immune cells may be used as an independent factor to evaluate the prognosis of patients with BTC.
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spelling pubmed-106513712022-12-13 The Expression of Programmed Death-Ligand 1 on Immune Cells Is Related to a Better Prognosis in Biliary Tract Cancer Kwon, Sung Chan Bang, Seungmin Park, Young Nyun Park, Ji Hoon Kim, So Jeong Jo, Jung Hyun Chung, Moon Jae Park, Jeong Youp Park, Seung Woo Song, Si Young Park, Eunhyang Lee, Hee Seung Gut Liver Original Article BACKGROUND/AIMS: Programmed death-ligand 1 (PD-L1) expression in tumor cells is associated with a poor biliary tract cancer (BTC) prognosis; tumor-infiltrating immune cells in the tumor microenvironment are associated with a better prognosis. The effect of PD-L1 expression on immune cells on survival is unclear. We investigated the relationship between PD-L1 expression in immune cells and BTC prognosis. METHODS: PD-L1 expression was evaluated using an anti-PD-L1 22C3 mouse monoclonal primary antibody, and its relationships with clinical characteristics and prognosis were analyzed using the Cox proportional hazard model to investigate the prognostic performance of PD-L1 in BTC. RESULTS: Among 144 analyzed cases, patients with positive PD-L1 expression in tumor cells and negative PD-L1 expression in immune cells showed poorer overall survival rates than those exhibiting other expressions (tumor cells hazard ratio [HR]=1.023, p<0.001; immune cells HR=0.983, p=0.021). PD-L1 expression in tumor cells was an independent predictor of poor overall survival (HR=1.024, p<0.001). In contrast, PD-L1 expression in immune cells was a predictive marker of good prognosis (HR=0.983, p=0.018). CONCLUSIONS: PD-L1 expression in immune cells may be used as an independent factor to evaluate the prognosis of patients with BTC. Editorial Office of Gut and Liver 2023-11-15 2022-12-13 /pmc/articles/PMC10651371/ /pubmed/36510775 http://dx.doi.org/10.5009/gnl220206 Text en Copyright © Gut and Liver. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kwon, Sung Chan
Bang, Seungmin
Park, Young Nyun
Park, Ji Hoon
Kim, So Jeong
Jo, Jung Hyun
Chung, Moon Jae
Park, Jeong Youp
Park, Seung Woo
Song, Si Young
Park, Eunhyang
Lee, Hee Seung
The Expression of Programmed Death-Ligand 1 on Immune Cells Is Related to a Better Prognosis in Biliary Tract Cancer
title The Expression of Programmed Death-Ligand 1 on Immune Cells Is Related to a Better Prognosis in Biliary Tract Cancer
title_full The Expression of Programmed Death-Ligand 1 on Immune Cells Is Related to a Better Prognosis in Biliary Tract Cancer
title_fullStr The Expression of Programmed Death-Ligand 1 on Immune Cells Is Related to a Better Prognosis in Biliary Tract Cancer
title_full_unstemmed The Expression of Programmed Death-Ligand 1 on Immune Cells Is Related to a Better Prognosis in Biliary Tract Cancer
title_short The Expression of Programmed Death-Ligand 1 on Immune Cells Is Related to a Better Prognosis in Biliary Tract Cancer
title_sort expression of programmed death-ligand 1 on immune cells is related to a better prognosis in biliary tract cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651371/
https://www.ncbi.nlm.nih.gov/pubmed/36510775
http://dx.doi.org/10.5009/gnl220206
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