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A novel model of liver cancer stem cells developed from induced pluripotent stem cells
BACKGROUND: Liver cancer is the second most common cause of cancer-related death. Every type of tumours including liver cancer contains cancer stem cells (CSCs). To date, the molecular mechanism regulating the development of liver CSCs remains unknown. METHODS: In this study, we tried to generate a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188674/ https://www.ncbi.nlm.nih.gov/pubmed/32203212 http://dx.doi.org/10.1038/s41416-020-0792-z |
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author | Afify, Said M. Sanchez Calle, Anna Hassan, Ghmkin Kumon, Kazuki Nawara, Hend M. Zahra, Maram H. Mansour, Hager M. Khayrani, Apriliana Cahya Alam, Md Jahangir Du, Juan Seno, Akimasa Iwasaki, Yoshiaki Seno, Masaharu |
author_facet | Afify, Said M. Sanchez Calle, Anna Hassan, Ghmkin Kumon, Kazuki Nawara, Hend M. Zahra, Maram H. Mansour, Hager M. Khayrani, Apriliana Cahya Alam, Md Jahangir Du, Juan Seno, Akimasa Iwasaki, Yoshiaki Seno, Masaharu |
author_sort | Afify, Said M. |
collection | PubMed |
description | BACKGROUND: Liver cancer is the second most common cause of cancer-related death. Every type of tumours including liver cancer contains cancer stem cells (CSCs). To date, the molecular mechanism regulating the development of liver CSCs remains unknown. METHODS: In this study, we tried to generate a new model of liver CSCs by converting mouse induced pluripotent stem cells (miPSCs) with hepatocellular carcinoma (HCC) cell line Huh7 cells conditioned medium (CM). miPSCs treated with CM were injected into the liver of BALB/c nude mice. The developed tumours were then excised and analysed. RESULTS: The primary cultured cells from the malignant tumour possessed self-renewal capacity, differentiation potential and tumorigenicity in vivo, which were found rich in liver cancer-associated markers as well as CSC markers. CONCLUSIONS: We established a model of liver CSCs converting from miPS and showed different stages of stemness during conversion process. Our CSC model will be important to assess the molecular mechanisms necessary to develop liver CSCs and could help in defeating liver cancer. |
format | Online Article Text |
id | pubmed-7188674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71886742020-05-01 A novel model of liver cancer stem cells developed from induced pluripotent stem cells Afify, Said M. Sanchez Calle, Anna Hassan, Ghmkin Kumon, Kazuki Nawara, Hend M. Zahra, Maram H. Mansour, Hager M. Khayrani, Apriliana Cahya Alam, Md Jahangir Du, Juan Seno, Akimasa Iwasaki, Yoshiaki Seno, Masaharu Br J Cancer Article BACKGROUND: Liver cancer is the second most common cause of cancer-related death. Every type of tumours including liver cancer contains cancer stem cells (CSCs). To date, the molecular mechanism regulating the development of liver CSCs remains unknown. METHODS: In this study, we tried to generate a new model of liver CSCs by converting mouse induced pluripotent stem cells (miPSCs) with hepatocellular carcinoma (HCC) cell line Huh7 cells conditioned medium (CM). miPSCs treated with CM were injected into the liver of BALB/c nude mice. The developed tumours were then excised and analysed. RESULTS: The primary cultured cells from the malignant tumour possessed self-renewal capacity, differentiation potential and tumorigenicity in vivo, which were found rich in liver cancer-associated markers as well as CSC markers. CONCLUSIONS: We established a model of liver CSCs converting from miPS and showed different stages of stemness during conversion process. Our CSC model will be important to assess the molecular mechanisms necessary to develop liver CSCs and could help in defeating liver cancer. Nature Publishing Group UK 2020-03-17 2020-04-28 /pmc/articles/PMC7188674/ /pubmed/32203212 http://dx.doi.org/10.1038/s41416-020-0792-z Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Afify, Said M. Sanchez Calle, Anna Hassan, Ghmkin Kumon, Kazuki Nawara, Hend M. Zahra, Maram H. Mansour, Hager M. Khayrani, Apriliana Cahya Alam, Md Jahangir Du, Juan Seno, Akimasa Iwasaki, Yoshiaki Seno, Masaharu A novel model of liver cancer stem cells developed from induced pluripotent stem cells |
title | A novel model of liver cancer stem cells developed from induced pluripotent stem cells |
title_full | A novel model of liver cancer stem cells developed from induced pluripotent stem cells |
title_fullStr | A novel model of liver cancer stem cells developed from induced pluripotent stem cells |
title_full_unstemmed | A novel model of liver cancer stem cells developed from induced pluripotent stem cells |
title_short | A novel model of liver cancer stem cells developed from induced pluripotent stem cells |
title_sort | novel model of liver cancer stem cells developed from induced pluripotent stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188674/ https://www.ncbi.nlm.nih.gov/pubmed/32203212 http://dx.doi.org/10.1038/s41416-020-0792-z |
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