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Three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments

Colorectal cancer demonstrates intra-tumour heterogeneity formed by a hierarchical structure comprised of cancer stem cells (CSCs) and their differentiated progenies. The mechanism by which CSCs are maintained and differentiated needs to be further elucidated, and there is evidence that the tumour m...

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Autores principales: Kawai, Shigeto, Yamazaki, Masaki, Shibuya, Keita, Yamazaki, Masaya, Fujii, Etsuko, Nakano, Kiyotaka, Suzuki, Masami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035265/
https://www.ncbi.nlm.nih.gov/pubmed/32081957
http://dx.doi.org/10.1038/s41598-020-60145-9
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author Kawai, Shigeto
Yamazaki, Masaki
Shibuya, Keita
Yamazaki, Masaya
Fujii, Etsuko
Nakano, Kiyotaka
Suzuki, Masami
author_facet Kawai, Shigeto
Yamazaki, Masaki
Shibuya, Keita
Yamazaki, Masaya
Fujii, Etsuko
Nakano, Kiyotaka
Suzuki, Masami
author_sort Kawai, Shigeto
collection PubMed
description Colorectal cancer demonstrates intra-tumour heterogeneity formed by a hierarchical structure comprised of cancer stem cells (CSCs) and their differentiated progenies. The mechanism by which CSCs are maintained and differentiated needs to be further elucidated, and there is evidence that the tumour microenvironment governs cancer stemness. Using PLR123, a colon cancer cell line with CSC properties, we determined the culture conditions necessary to establish a pair of three-dimensional (3D) culture models grown in Matrigel, designated stemCO and diffCO. The conditions were determined by comparing the phenotypes in the models with PLR123 mouse xenografts colonising lung and liver. StemCO resembled LGR5-positive undifferentiated tumours in the lung, and diffCO had lumen structures composed of polarised cells that were similar to the ductal structures found in differentiated tumours in the liver. In a case using the models for biomedical research, treatment with JAG-1 peptide or a γ-secretase inhibitor modified the Notch signaling and induced changes indicating that the signal participates in lumen formation in the models. Our results demonstrate that culture conditions affect the stemness of 3D culture models generated from CSCs and show that comparing models with different phenotypes is useful for studying how the tumour environment regulates cancer.
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spelling pubmed-70352652020-02-28 Three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments Kawai, Shigeto Yamazaki, Masaki Shibuya, Keita Yamazaki, Masaya Fujii, Etsuko Nakano, Kiyotaka Suzuki, Masami Sci Rep Article Colorectal cancer demonstrates intra-tumour heterogeneity formed by a hierarchical structure comprised of cancer stem cells (CSCs) and their differentiated progenies. The mechanism by which CSCs are maintained and differentiated needs to be further elucidated, and there is evidence that the tumour microenvironment governs cancer stemness. Using PLR123, a colon cancer cell line with CSC properties, we determined the culture conditions necessary to establish a pair of three-dimensional (3D) culture models grown in Matrigel, designated stemCO and diffCO. The conditions were determined by comparing the phenotypes in the models with PLR123 mouse xenografts colonising lung and liver. StemCO resembled LGR5-positive undifferentiated tumours in the lung, and diffCO had lumen structures composed of polarised cells that were similar to the ductal structures found in differentiated tumours in the liver. In a case using the models for biomedical research, treatment with JAG-1 peptide or a γ-secretase inhibitor modified the Notch signaling and induced changes indicating that the signal participates in lumen formation in the models. Our results demonstrate that culture conditions affect the stemness of 3D culture models generated from CSCs and show that comparing models with different phenotypes is useful for studying how the tumour environment regulates cancer. Nature Publishing Group UK 2020-02-21 /pmc/articles/PMC7035265/ /pubmed/32081957 http://dx.doi.org/10.1038/s41598-020-60145-9 Text en © The Author(s) 2020 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/.
spellingShingle Article
Kawai, Shigeto
Yamazaki, Masaki
Shibuya, Keita
Yamazaki, Masaya
Fujii, Etsuko
Nakano, Kiyotaka
Suzuki, Masami
Three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments
title Three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments
title_full Three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments
title_fullStr Three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments
title_full_unstemmed Three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments
title_short Three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments
title_sort three-dimensional culture models mimic colon cancer heterogeneity induced by different microenvironments
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035265/
https://www.ncbi.nlm.nih.gov/pubmed/32081957
http://dx.doi.org/10.1038/s41598-020-60145-9
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