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  Decoding cell-type contributions to the cfRNA transcriptomic landscape of liver cancer

Safrastyan, A., zu Siederdissen, C. H., & Wollny, D. (2023). Decoding cell-type contributions to the cfRNA transcriptomic landscape of liver cancer. Human Genomics, 17(1):. doi:10.1186/s40246-023-00537-w.

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-000D-CEB4-0 版のパーマリンク: https://hdl.handle.net/21.11116/0000-000D-CEB5-F
資料種別: 学術論文

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Safrastyan_Decoding_HumGen_2023.pdf (出版社版), 3MB
ファイルのパーマリンク:
https://hdl.handle.net/21.11116/0000-000D-CEB6-E
ファイル名:
Safrastyan_Decoding_HumGen_2023.pdf
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-
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Gold
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公開
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application/pdf / [MD5]
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著作権日付:
2023
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 作成者:
Safrastyan, Aram, 著者
zu Siederdissen, Christian Höner, 著者
Wollny, Damian1, 著者                 
所属:
1Single Cell Genomics, Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Max Planck Society, ou_2173644              

内容説明

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キーワード: Cell-free RNA; Cellular deconvolution; Liquid biopsy; Liver cancer; Modeling; Single-cell sequencing
 要旨: Background: Liquid biopsy, particularly cell-free RNA (cfRNA), has emerged as a promising non-invasive diagnostic tool for various diseases, including cancer, due to its accessibility and the wealth of information it provides. A key area of interest is the composition and cellular origin of cfRNA in the blood and the alterations in the cfRNA transcriptomic landscape during carcinogenesis. Investigating these changes can offer insights into the manifestations of tissue alterations in the blood, potentially leading to more effective diagnostic strategies. However, the consistency of these findings across different studies and their clinical utility remains to be fully elucidated, highlighting the need for further research in this area. Results: In this study, we analyzed over 350 blood samples from four distinct studies, investigating the cell type contributions to the cfRNA transcriptomic landscape in liver cancer. We found that an increase in hepatocyte proportions in the blood is a consistent feature across most studies and can be effectively utilized for classifying cancer and healthy samples. Moreover, our analysis revealed that in addition to hepatocytes, liver endothelial cell signatures are also prominent in the observed changes. By comparing the classification performance of cellular proportions to established markers, we demonstrated that cellular proportions could distinguish cancer from healthy samples as effectively as existing markers and can even enhance classification when used in combination with these markers. Conclusions: Our comprehensive analysis of liver cell-type composition changes in blood revealed robust effects that help classify cancer from healthy samples. This is especially noteworthy, considering the heterogeneous nature of datasets and the etiological distinctions of samples. Furthermore, the observed differences in results across studies underscore the importance of integrative and comparative approaches in the future research to determine the consistency and robustness of findings. This study contributes to the understanding of cfRNA composition in liver cancer and highlights the potential of cellular deconvolution in liquid biopsy. © 2023, BioMed Central Ltd., part of Springer Nature.

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言語: eng - English
 日付: 2023-10-052023-12
 出版の状態: 出版
 ページ: -
 出版情報: -
 目次: -
 査読: 査読あり
 識別子(DOI, ISBNなど): DOI: 10.1186/s40246-023-00537-w
 学位: -

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出版物 1

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出版物名: Human Genomics
種別: 学術雑誌
 著者・編者:
所属:
出版社, 出版地: -
ページ: - 巻号: 17 (1) 通巻号: 90 開始・終了ページ: - 識別子(ISBN, ISSN, DOIなど): ISSN: 1479-7364