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Reciprocal Interaction of Cancer Stem Cells of Cholangiocarcinoma with Macrophage

Cholangiocarcinoma is an aggressive type of liver cancer with few effective treatment options. Therefore, there is great need to better understand the biology of this malignancy to further development of novel treatment options. Cancer stem cells (CSCs) are thought to the underlying reason for cance...

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Autores principales: Wang, Xin, Golino, Jihye L., Hawk, Nga Voong, Xie, Changqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390592/
https://www.ncbi.nlm.nih.gov/pubmed/37249733
http://dx.doi.org/10.1007/s12015-023-10557-7
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author Wang, Xin
Golino, Jihye L.
Hawk, Nga Voong
Xie, Changqing
author_facet Wang, Xin
Golino, Jihye L.
Hawk, Nga Voong
Xie, Changqing
author_sort Wang, Xin
collection PubMed
description Cholangiocarcinoma is an aggressive type of liver cancer with few effective treatment options. Therefore, there is great need to better understand the biology of this malignancy to further development of novel treatment options. Cancer stem cells (CSCs) are thought to the underlying reason for cancer initiation, metastasis, and relapse. However, due to their elusive character and differences in identification among different types of cancer, it remains a challenge to study such cells. Additionally, characterization of the tumor microenvironment such as interactions with immune cells remain largely unknown. Here, we employ a fluorescent reporter system to track and isolate stem-like cancer cells of cholangiocarcinoma cell lines. Following verification of a stem-like signature (upregulated expression of stemness markers, resistance to chemotherapy, increased spheroid formation, and tumorigenesis capabilities despite inoculation of a small number of cells), we analyzed the interaction of these cells with macrophages via direct and indirect coculture assays. We noted direct coculturing increased stemness among CSC populations and induced both M1 (CD80 and HLA-DR) and M2 (CD163) tumor associated macrophage polarization. These studies suggest that there is a bi-directional crosstalk between macrophages and CSCs that promotes stemness renewal and tumor associated macrophage polarization. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12015-023-10557-7.
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spelling pubmed-103905922023-08-02 Reciprocal Interaction of Cancer Stem Cells of Cholangiocarcinoma with Macrophage Wang, Xin Golino, Jihye L. Hawk, Nga Voong Xie, Changqing Stem Cell Rev Rep Article Cholangiocarcinoma is an aggressive type of liver cancer with few effective treatment options. Therefore, there is great need to better understand the biology of this malignancy to further development of novel treatment options. Cancer stem cells (CSCs) are thought to the underlying reason for cancer initiation, metastasis, and relapse. However, due to their elusive character and differences in identification among different types of cancer, it remains a challenge to study such cells. Additionally, characterization of the tumor microenvironment such as interactions with immune cells remain largely unknown. Here, we employ a fluorescent reporter system to track and isolate stem-like cancer cells of cholangiocarcinoma cell lines. Following verification of a stem-like signature (upregulated expression of stemness markers, resistance to chemotherapy, increased spheroid formation, and tumorigenesis capabilities despite inoculation of a small number of cells), we analyzed the interaction of these cells with macrophages via direct and indirect coculture assays. We noted direct coculturing increased stemness among CSC populations and induced both M1 (CD80 and HLA-DR) and M2 (CD163) tumor associated macrophage polarization. These studies suggest that there is a bi-directional crosstalk between macrophages and CSCs that promotes stemness renewal and tumor associated macrophage polarization. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12015-023-10557-7. Springer US 2023-05-30 2023 /pmc/articles/PMC10390592/ /pubmed/37249733 http://dx.doi.org/10.1007/s12015-023-10557-7 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 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/) .
spellingShingle Article
Wang, Xin
Golino, Jihye L.
Hawk, Nga Voong
Xie, Changqing
Reciprocal Interaction of Cancer Stem Cells of Cholangiocarcinoma with Macrophage
title Reciprocal Interaction of Cancer Stem Cells of Cholangiocarcinoma with Macrophage
title_full Reciprocal Interaction of Cancer Stem Cells of Cholangiocarcinoma with Macrophage
title_fullStr Reciprocal Interaction of Cancer Stem Cells of Cholangiocarcinoma with Macrophage
title_full_unstemmed Reciprocal Interaction of Cancer Stem Cells of Cholangiocarcinoma with Macrophage
title_short Reciprocal Interaction of Cancer Stem Cells of Cholangiocarcinoma with Macrophage
title_sort reciprocal interaction of cancer stem cells of cholangiocarcinoma with macrophage
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390592/
https://www.ncbi.nlm.nih.gov/pubmed/37249733
http://dx.doi.org/10.1007/s12015-023-10557-7
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