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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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Detalles Bibliográficos
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
Descripción
Sumario: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.