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Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures

BACKGROUND: Although biological resources are essential for basic and preclinical research in the oncological field, those of sarcoma are not sufficient for rapid development of the treatment. So far, some sarcoma cell lines have been established, however, the success rate was low and the establishe...

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Autores principales: Wakamatsu, Toru, Ogawa, Hisataka, Yoshida, Keiichi, Matsuoka, Yukiko, Shizuma, Kazuko, Imura, Yoshinori, Tamiya, Hironari, Nakai, Sho, Yagi, Toshinari, Nagata, Shigenori, Yui, Yoshihiro, Sasagawa, Satoru, Takenaka, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169059/
https://www.ncbi.nlm.nih.gov/pubmed/35677170
http://dx.doi.org/10.3389/fonc.2022.893592
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author Wakamatsu, Toru
Ogawa, Hisataka
Yoshida, Keiichi
Matsuoka, Yukiko
Shizuma, Kazuko
Imura, Yoshinori
Tamiya, Hironari
Nakai, Sho
Yagi, Toshinari
Nagata, Shigenori
Yui, Yoshihiro
Sasagawa, Satoru
Takenaka, Satoshi
author_facet Wakamatsu, Toru
Ogawa, Hisataka
Yoshida, Keiichi
Matsuoka, Yukiko
Shizuma, Kazuko
Imura, Yoshinori
Tamiya, Hironari
Nakai, Sho
Yagi, Toshinari
Nagata, Shigenori
Yui, Yoshihiro
Sasagawa, Satoru
Takenaka, Satoshi
author_sort Wakamatsu, Toru
collection PubMed
description BACKGROUND: Although biological resources are essential for basic and preclinical research in the oncological field, those of sarcoma are not sufficient for rapid development of the treatment. So far, some sarcoma cell lines have been established, however, the success rate was low and the established sarcoma types were frequently biased. Therefore, an efficient culture method is needed to determine the various types of sarcomas. Organoid culture is a 3-dimentional culture method that enables the recapitulation of the tumor microenvironment and the success rate reported is higher than the 2-dimentional culture. The purpose of this study was to report our newly established organoids from human epithelioid sarcoma using the air-liquid interface organoid culture method. METHODS: We treated 2 patients with epithelioid sarcoma in our institute. The remaining sarcoma specimens after surgical resection were embedded in collagen type 1 gels according to the air-liquid interface organoid culture method. After serial passages, we xenografted the organoids to NOD-scid IL2Rgnull (NSG) mice. Using the developed tumors, we performed histological and genomic analyses to compare the similarities and differences with the original epithelioid sarcoma from the patient. RESULTS: Organoids from the epithelioid sarcoma could be serially cultured and maintained in collagen type 1 gels for more than 3 passages. Developed orthotopic tumor xenografts were detected in the NSG mice. After the process was repeated severally, the patient derived organoid lines from the epithelioid sarcoma were established. The established organoids showed loss of integrase interactor 1 expression with polymerase chain reaction and immunohistochemical analyses. The xenografted organoids of the epithelioid sarcoma had histologically similar phenotypes with the original tumor and genetically resembled it to some degree. CONCLUSIONS: The present study demonstrated 2 novel established organoid models of epithelioid sarcoma, and our organoid models could be used to investigate the molecular pathogenesis and develop a novel treatment.
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spelling pubmed-91690592022-06-07 Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures Wakamatsu, Toru Ogawa, Hisataka Yoshida, Keiichi Matsuoka, Yukiko Shizuma, Kazuko Imura, Yoshinori Tamiya, Hironari Nakai, Sho Yagi, Toshinari Nagata, Shigenori Yui, Yoshihiro Sasagawa, Satoru Takenaka, Satoshi Front Oncol Oncology BACKGROUND: Although biological resources are essential for basic and preclinical research in the oncological field, those of sarcoma are not sufficient for rapid development of the treatment. So far, some sarcoma cell lines have been established, however, the success rate was low and the established sarcoma types were frequently biased. Therefore, an efficient culture method is needed to determine the various types of sarcomas. Organoid culture is a 3-dimentional culture method that enables the recapitulation of the tumor microenvironment and the success rate reported is higher than the 2-dimentional culture. The purpose of this study was to report our newly established organoids from human epithelioid sarcoma using the air-liquid interface organoid culture method. METHODS: We treated 2 patients with epithelioid sarcoma in our institute. The remaining sarcoma specimens after surgical resection were embedded in collagen type 1 gels according to the air-liquid interface organoid culture method. After serial passages, we xenografted the organoids to NOD-scid IL2Rgnull (NSG) mice. Using the developed tumors, we performed histological and genomic analyses to compare the similarities and differences with the original epithelioid sarcoma from the patient. RESULTS: Organoids from the epithelioid sarcoma could be serially cultured and maintained in collagen type 1 gels for more than 3 passages. Developed orthotopic tumor xenografts were detected in the NSG mice. After the process was repeated severally, the patient derived organoid lines from the epithelioid sarcoma were established. The established organoids showed loss of integrase interactor 1 expression with polymerase chain reaction and immunohistochemical analyses. The xenografted organoids of the epithelioid sarcoma had histologically similar phenotypes with the original tumor and genetically resembled it to some degree. CONCLUSIONS: The present study demonstrated 2 novel established organoid models of epithelioid sarcoma, and our organoid models could be used to investigate the molecular pathogenesis and develop a novel treatment. Frontiers Media S.A. 2022-05-23 /pmc/articles/PMC9169059/ /pubmed/35677170 http://dx.doi.org/10.3389/fonc.2022.893592 Text en Copyright © 2022 Wakamatsu, Ogawa, Yoshida, Matsuoka, Shizuma, Imura, Tamiya, Nakai, Yagi, Nagata, Yui, Sasagawa and Takenaka https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Wakamatsu, Toru
Ogawa, Hisataka
Yoshida, Keiichi
Matsuoka, Yukiko
Shizuma, Kazuko
Imura, Yoshinori
Tamiya, Hironari
Nakai, Sho
Yagi, Toshinari
Nagata, Shigenori
Yui, Yoshihiro
Sasagawa, Satoru
Takenaka, Satoshi
Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures
title Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures
title_full Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures
title_fullStr Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures
title_full_unstemmed Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures
title_short Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures
title_sort establishment of organoids from human epithelioid sarcoma with the air-liquid interface organoid cultures
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169059/
https://www.ncbi.nlm.nih.gov/pubmed/35677170
http://dx.doi.org/10.3389/fonc.2022.893592
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