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Immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes

BACKGROUND: Anti-tumour immune competence has an impact in hepatocarcinogenesis and success of anti-cancer therapies. Tumour-infiltrating lymphocytes (TILs) and monocytes/macrophages (TAMs) are proposed to have significance in cancer. However, there is only limited data concerning their impact on pa...

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Autores principales: Atanasov, Georgi, Dino, Karoline, Schierle, Katrin, Dietel, Corinna, Aust, Gabriela, Pratschke, Johann, Seehofer, Daniel, Schmelzle, Moritz, Hau, Hans-Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554997/
https://www.ncbi.nlm.nih.gov/pubmed/31170995
http://dx.doi.org/10.1186/s12957-019-1635-3
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author Atanasov, Georgi
Dino, Karoline
Schierle, Katrin
Dietel, Corinna
Aust, Gabriela
Pratschke, Johann
Seehofer, Daniel
Schmelzle, Moritz
Hau, Hans-Michael
author_facet Atanasov, Georgi
Dino, Karoline
Schierle, Katrin
Dietel, Corinna
Aust, Gabriela
Pratschke, Johann
Seehofer, Daniel
Schmelzle, Moritz
Hau, Hans-Michael
author_sort Atanasov, Georgi
collection PubMed
description BACKGROUND: Anti-tumour immune competence has an impact in hepatocarcinogenesis and success of anti-cancer therapies. Tumour-infiltrating lymphocytes (TILs) and monocytes/macrophages (TAMs) are proposed to have significance in cancer. However, there is only limited data concerning their impact on patient outcome and survival in hepatocellular carcinoma (HCC). METHODS: Frequencies of CD68(+), CD163(+) M2-polarized TAMs and TILs were measured in de novo HCC tumours in non-cirrhosis (n = 58) using immunohistology and correlated to patients’ clinicopathological characteristics and survival rates. RESULTS: Patients with tumours marked by appearance of TILs and CD68(+) TAMs showed an improved 1-, 3- and 5-year recurrence-free survival (all p ≤ 0.05). CD68(+) TAMs were associated with reduced incidence of recurrent and multifocal disease. Conversely, CD163(+) TAMs were associated with multifocal HCC and lymphangiosis carcinomatosa (all p ≤ 0.05). CONCLUSIONS: TILs and CD68(+) TAMs are associated with multiple tumour characteristics and patient survival in HCC. However, there is only scarce data about the biology underlying their mechanistic involvement in human tumour progression. Thus, experimental data on functional links might help develop novel immunologic checkpoint inhibitor targets for liver cancer.
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spelling pubmed-65549972019-06-10 Immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes Atanasov, Georgi Dino, Karoline Schierle, Katrin Dietel, Corinna Aust, Gabriela Pratschke, Johann Seehofer, Daniel Schmelzle, Moritz Hau, Hans-Michael World J Surg Oncol Research BACKGROUND: Anti-tumour immune competence has an impact in hepatocarcinogenesis and success of anti-cancer therapies. Tumour-infiltrating lymphocytes (TILs) and monocytes/macrophages (TAMs) are proposed to have significance in cancer. However, there is only limited data concerning their impact on patient outcome and survival in hepatocellular carcinoma (HCC). METHODS: Frequencies of CD68(+), CD163(+) M2-polarized TAMs and TILs were measured in de novo HCC tumours in non-cirrhosis (n = 58) using immunohistology and correlated to patients’ clinicopathological characteristics and survival rates. RESULTS: Patients with tumours marked by appearance of TILs and CD68(+) TAMs showed an improved 1-, 3- and 5-year recurrence-free survival (all p ≤ 0.05). CD68(+) TAMs were associated with reduced incidence of recurrent and multifocal disease. Conversely, CD163(+) TAMs were associated with multifocal HCC and lymphangiosis carcinomatosa (all p ≤ 0.05). CONCLUSIONS: TILs and CD68(+) TAMs are associated with multiple tumour characteristics and patient survival in HCC. However, there is only scarce data about the biology underlying their mechanistic involvement in human tumour progression. Thus, experimental data on functional links might help develop novel immunologic checkpoint inhibitor targets for liver cancer. BioMed Central 2019-06-06 /pmc/articles/PMC6554997/ /pubmed/31170995 http://dx.doi.org/10.1186/s12957-019-1635-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Atanasov, Georgi
Dino, Karoline
Schierle, Katrin
Dietel, Corinna
Aust, Gabriela
Pratschke, Johann
Seehofer, Daniel
Schmelzle, Moritz
Hau, Hans-Michael
Immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes
title Immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes
title_full Immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes
title_fullStr Immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes
title_full_unstemmed Immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes
title_short Immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes
title_sort immunologic cellular characteristics of the tumour microenvironment of hepatocellular carcinoma drive patient outcomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554997/
https://www.ncbi.nlm.nih.gov/pubmed/31170995
http://dx.doi.org/10.1186/s12957-019-1635-3
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