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Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens

Single-cell level analysis is powerful tool to assess the heterogeneity of cellular components in tumor microenvironments (TME). In this study, we investigated immune-profiles using the single-cell analyses of endoscopically- or surgically-resected tumors, and peripheral blood mononuclear cells from...

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Autores principales: Kashima, Yukie, Togashi, Yosuke, Fukuoka, Shota, Kamada, Takahiro, Irie, Takuma, Suzuki, Ayako, Nakamura, Yoshiaki, Shitara, Kohei, Minamide, Tatsunori, Yoshida, Taku, Taoka, Naofumi, Kawase, Tatsuya, Wada, Teiji, Inaki, Koichiro, Chihara, Masataka, Ebisuno, Yukihiko, Tsukamoto, Sakiyo, Fujii, Ryo, Ohashi, Akihiro, Suzuki, Yutaka, Tsuchihara, Katsuya, Nishikawa, Hiroyoshi, Doi, Toshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801605/
https://www.ncbi.nlm.nih.gov/pubmed/33431933
http://dx.doi.org/10.1038/s41598-020-79385-w
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author Kashima, Yukie
Togashi, Yosuke
Fukuoka, Shota
Kamada, Takahiro
Irie, Takuma
Suzuki, Ayako
Nakamura, Yoshiaki
Shitara, Kohei
Minamide, Tatsunori
Yoshida, Taku
Taoka, Naofumi
Kawase, Tatsuya
Wada, Teiji
Inaki, Koichiro
Chihara, Masataka
Ebisuno, Yukihiko
Tsukamoto, Sakiyo
Fujii, Ryo
Ohashi, Akihiro
Suzuki, Yutaka
Tsuchihara, Katsuya
Nishikawa, Hiroyoshi
Doi, Toshihiko
author_facet Kashima, Yukie
Togashi, Yosuke
Fukuoka, Shota
Kamada, Takahiro
Irie, Takuma
Suzuki, Ayako
Nakamura, Yoshiaki
Shitara, Kohei
Minamide, Tatsunori
Yoshida, Taku
Taoka, Naofumi
Kawase, Tatsuya
Wada, Teiji
Inaki, Koichiro
Chihara, Masataka
Ebisuno, Yukihiko
Tsukamoto, Sakiyo
Fujii, Ryo
Ohashi, Akihiro
Suzuki, Yutaka
Tsuchihara, Katsuya
Nishikawa, Hiroyoshi
Doi, Toshihiko
author_sort Kashima, Yukie
collection PubMed
description Single-cell level analysis is powerful tool to assess the heterogeneity of cellular components in tumor microenvironments (TME). In this study, we investigated immune-profiles using the single-cell analyses of endoscopically- or surgically-resected tumors, and peripheral blood mononuclear cells from gastric cancer patients. Furthermore, we technically characterized two distinct platforms of the single-cell analysis; RNA-seq-based analysis (scRNA-seq), and mass cytometry-based analysis (CyTOF), both of which are broadly embraced technologies. Our study revealed that the scRNA-seq analysis could cover a broader range of immune cells of TME in the biopsy-resected small samples of tumors, detecting even small subgroups of B cells or Treg cells in the tumors, although CyTOF could distinguish the specific populations in more depth. These findings demonstrate that scRNA-seq analysis is a highly-feasible platform for elucidating the complexity of TME in small biopsy tumors, which would provide a novel strategies to overcome a therapeutic difficulties against cancer heterogeneity in TME.
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spelling pubmed-78016052021-01-12 Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens Kashima, Yukie Togashi, Yosuke Fukuoka, Shota Kamada, Takahiro Irie, Takuma Suzuki, Ayako Nakamura, Yoshiaki Shitara, Kohei Minamide, Tatsunori Yoshida, Taku Taoka, Naofumi Kawase, Tatsuya Wada, Teiji Inaki, Koichiro Chihara, Masataka Ebisuno, Yukihiko Tsukamoto, Sakiyo Fujii, Ryo Ohashi, Akihiro Suzuki, Yutaka Tsuchihara, Katsuya Nishikawa, Hiroyoshi Doi, Toshihiko Sci Rep Article Single-cell level analysis is powerful tool to assess the heterogeneity of cellular components in tumor microenvironments (TME). In this study, we investigated immune-profiles using the single-cell analyses of endoscopically- or surgically-resected tumors, and peripheral blood mononuclear cells from gastric cancer patients. Furthermore, we technically characterized two distinct platforms of the single-cell analysis; RNA-seq-based analysis (scRNA-seq), and mass cytometry-based analysis (CyTOF), both of which are broadly embraced technologies. Our study revealed that the scRNA-seq analysis could cover a broader range of immune cells of TME in the biopsy-resected small samples of tumors, detecting even small subgroups of B cells or Treg cells in the tumors, although CyTOF could distinguish the specific populations in more depth. These findings demonstrate that scRNA-seq analysis is a highly-feasible platform for elucidating the complexity of TME in small biopsy tumors, which would provide a novel strategies to overcome a therapeutic difficulties against cancer heterogeneity in TME. Nature Publishing Group UK 2021-01-11 /pmc/articles/PMC7801605/ /pubmed/33431933 http://dx.doi.org/10.1038/s41598-020-79385-w Text en © The Author(s) 2021 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/.
spellingShingle Article
Kashima, Yukie
Togashi, Yosuke
Fukuoka, Shota
Kamada, Takahiro
Irie, Takuma
Suzuki, Ayako
Nakamura, Yoshiaki
Shitara, Kohei
Minamide, Tatsunori
Yoshida, Taku
Taoka, Naofumi
Kawase, Tatsuya
Wada, Teiji
Inaki, Koichiro
Chihara, Masataka
Ebisuno, Yukihiko
Tsukamoto, Sakiyo
Fujii, Ryo
Ohashi, Akihiro
Suzuki, Yutaka
Tsuchihara, Katsuya
Nishikawa, Hiroyoshi
Doi, Toshihiko
Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens
title Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens
title_full Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens
title_fullStr Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens
title_full_unstemmed Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens
title_short Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens
title_sort potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801605/
https://www.ncbi.nlm.nih.gov/pubmed/33431933
http://dx.doi.org/10.1038/s41598-020-79385-w
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