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Systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma
BACKGROUND: Glioma is the most commonly diagnosed malignant and aggressive brain cancer in adults. Traditional researches mainly explored the expression profile of glioma at cell-population level, but ignored the heterogeneity and interactions of among glioma cells. METHODS: Here, we firstly analyze...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532229/ https://www.ncbi.nlm.nih.gov/pubmed/31118022 http://dx.doi.org/10.1186/s12964-019-0363-1 |
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author | Yuan, Dongsheng Tao, Yiran Chen, Geng Shi, Tieliu |
author_facet | Yuan, Dongsheng Tao, Yiran Chen, Geng Shi, Tieliu |
author_sort | Yuan, Dongsheng |
collection | PubMed |
description | BACKGROUND: Glioma is the most commonly diagnosed malignant and aggressive brain cancer in adults. Traditional researches mainly explored the expression profile of glioma at cell-population level, but ignored the heterogeneity and interactions of among glioma cells. METHODS: Here, we firstly analyzed the single-cell RNA-seq (scRNA-seq) data of 6341 glioma cells using manifold learning and identified neoplastic and healthy cells infiltrating in tumor microenvironment. We systematically revealed cell-to-cell interactions inside gliomas based on corresponding scRNA-seq and TCGA RNA-seq data. RESULTS: A total of 16 significantly correlated autocrine ligand-receptor signal pairs inside neoplastic cells were identified based on the scRNA-seq and TCGA data of glioma. Furthermore, we explored the intercellular communications between cancer stem-like cells (CSCs) and macrophages, and identified 66 ligand-receptor pairs, some of which could significantly affect prognostic outcomes. An efficient machine learning model was constructed to accurately predict the prognosis of glioma patients based on the ligand-receptor interactions. CONCLUSION: Collectively, our study not only reveals functionally important cell-to-cell interactions inside glioma, but also detects potentially prognostic markers for predicting the survival of glioma patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12964-019-0363-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6532229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65322292019-05-29 Systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma Yuan, Dongsheng Tao, Yiran Chen, Geng Shi, Tieliu Cell Commun Signal Research BACKGROUND: Glioma is the most commonly diagnosed malignant and aggressive brain cancer in adults. Traditional researches mainly explored the expression profile of glioma at cell-population level, but ignored the heterogeneity and interactions of among glioma cells. METHODS: Here, we firstly analyzed the single-cell RNA-seq (scRNA-seq) data of 6341 glioma cells using manifold learning and identified neoplastic and healthy cells infiltrating in tumor microenvironment. We systematically revealed cell-to-cell interactions inside gliomas based on corresponding scRNA-seq and TCGA RNA-seq data. RESULTS: A total of 16 significantly correlated autocrine ligand-receptor signal pairs inside neoplastic cells were identified based on the scRNA-seq and TCGA data of glioma. Furthermore, we explored the intercellular communications between cancer stem-like cells (CSCs) and macrophages, and identified 66 ligand-receptor pairs, some of which could significantly affect prognostic outcomes. An efficient machine learning model was constructed to accurately predict the prognosis of glioma patients based on the ligand-receptor interactions. CONCLUSION: Collectively, our study not only reveals functionally important cell-to-cell interactions inside glioma, but also detects potentially prognostic markers for predicting the survival of glioma patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12964-019-0363-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-22 /pmc/articles/PMC6532229/ /pubmed/31118022 http://dx.doi.org/10.1186/s12964-019-0363-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Yuan, Dongsheng Tao, Yiran Chen, Geng Shi, Tieliu Systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma |
title | Systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma |
title_full | Systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma |
title_fullStr | Systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma |
title_full_unstemmed | Systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma |
title_short | Systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma |
title_sort | systematic expression analysis of ligand-receptor pairs reveals important cell-to-cell interactions inside glioma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532229/ https://www.ncbi.nlm.nih.gov/pubmed/31118022 http://dx.doi.org/10.1186/s12964-019-0363-1 |
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