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Reproducible and sensitive micro-tissue RNA sequencing from formalin-fixed paraffin-embedded tissues for spatial gene expression analysis.
Matsunaga, Hiroko; Arikawa, Koji; Yamazaki, Miki; Wagatsuma, Ryota; Ide, Keigo; Samuel, Ashok Zachariah; Takamochi, Kazuya; Suzuki, Kenji; Hayashi, Takuo; Hosokawa, Masahito; Kambara, Hideki; Takeyama, Haruko.
Afiliação
  • Matsunaga H; Research Organization for Nano and Life Innovation, Waseda University, Tokyo, Japan.
  • Arikawa K; Research Organization for Nano and Life Innovation, Waseda University, Tokyo, Japan.
  • Yamazaki M; Department of Life Science and Medical Bioscience, Waseda University, Tokyo, Japan.
  • Wagatsuma R; Computational Bio Big-Data Open Innovation Laboratory, AIST-Waseda University, Tokyo, Japan.
  • Ide K; Department of Life Science and Medical Bioscience, Waseda University, Tokyo, Japan.
  • Samuel AZ; Computational Bio Big-Data Open Innovation Laboratory, AIST-Waseda University, Tokyo, Japan.
  • Takamochi K; Department of Life Science and Medical Bioscience, Waseda University, Tokyo, Japan.
  • Suzuki K; Computational Bio Big-Data Open Innovation Laboratory, AIST-Waseda University, Tokyo, Japan.
  • Hayashi T; Research Organization for Nano and Life Innovation, Waseda University, Tokyo, Japan.
  • Hosokawa M; Department of Thoracic Surgery, Juntendo University School of Medicine, Tokyo, Japan.
  • Kambara H; Department of Thoracic Surgery, Juntendo University School of Medicine, Tokyo, Japan.
  • Takeyama H; Department of Human Pathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Sci Rep ; 12(1): 19511, 2022 11 14.
Article em En | MEDLINE | ID: mdl-36376423
ABSTRACT
Spatial transcriptome analysis of formalin-fixed paraffin-embedded (FFPE) tissues using RNA-sequencing (RNA-seq) provides interactive information on morphology and gene expression, which is useful for clinical applications. However, despite the advantages of long-term storage at room temperature, FFPE tissues may be severely damaged by methylene crosslinking and provide less gene information than fresh-frozen tissues. In this study, we proposed a sensitive FFPE micro-tissue RNA-seq method that combines the punching of tissue sections (diameter 100 µm) and the direct construction of RNA-seq libraries. We evaluated a method using mouse liver tissues at two years after fixation and embedding and detected approximately 7000 genes in micro-punched tissue-spots (thickness 10 µm), similar to that detected with purified total RNA (2.5 ng) equivalent to the several dozen cells in the spot. We applied this method to clinical FFPE specimens of lung cancer that had been fixed and embedded 6 years prior, and found that it was possible to determine characteristic gene expression in the microenvironment containing tumor and non-tumor cells of different morphologies. This result indicates that spatial gene expression analysis of the tumor microenvironment is feasible using FFPE tissue sections stored for extensive periods in medical facilities.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão