Evidence map›Paper›PMID 39800874›Full record

ArticleBriefings in bioinformatics2024

CellMsg: graph convolutional networks for ligand-receptor-mediated cell-cell communication analysis.

Hong Xia, Boya Ji, Debin Qiao, Shaoliang Peng

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Hong XiaCollege of Computer Science and Electronic Engineering, Hunan University, Changsha 410082, China.
Boya JiCollege of Computer Science and Electronic Engineering, Hunan University, Changsha 410082, China.
Debin QiaoSchool of Computer and Artificial Intelligence, ZhengZhou University, Zhengzhou 450001, China.
Shaoliang PengCollege of Computer Science and Electronic Engineering, Hunan University, Changsha 410082, China.

Funding

Funds of State Key Laboratory of Chemo/Biosensing and ChemometricsGraduate Research Innovation Project of Hunan Province QL20230101Innovative Research Group Project of Hunan Province 2024JJ1002Key R&D Program of Hunan Province 2023GK2004Key Technologies R&D Program of Guangdong Province 2023B1111030004National Key R&D Program of China 2022YFC3400400National Supercomputing Center in Changsha, and Peng Cheng LabNSFC-FDCT 62361166662Top 10 Technical Key Project in Hunan Province 2023GK1010
6 · The paper itself

Abstract

The role of cell-cell communications (CCCs) is increasingly recognized as being important to differentiation, invasion, metastasis, and drug resistance in tumoral tissues. Developing CCC inference methods using traditional experimental methods are time-consuming, labor-intensive, cannot handle large amounts of data. To facilitate inference of CCCs, we proposed a computational framework, called CellMsg, which involves two primary steps: identifying ligand-receptor interactions (LRIs) and measuring the strength of LRIs-mediated CCCs. Specifically, CellMsg first identifies high-confident LRIs based on multimodal features of ligands and receptors and graph convolutional networks. Then, CellMsg measures the strength of intercellular communication by combining the identified LRIs and single-cell RNA-seq data using a three-point estimation method. Performance evaluation on four benchmark LRI datasets by five-fold cross validation demonstrated that CellMsg accurately captured the relationships between ligands and receptors, resulting in the identification of high-confident LRIs. Compared with other methods of identifying LRIs, CellMsg has better prediction performance and robustness. Furthermore, the LRIs identified by CellMsg were successfully validated through molecular docking. Finally, we examined the overlap of LRIs between CellMsg and five other classical CCC databases, as well as the intercellular crosstalk among seven cell types within a human melanoma tissue. In summary, CellMsg establishes a complete, reliable, and well-organized LRI database and an effective CCC strength evaluation method for each single-cell RNA-seq data. It provides a computational tool allowing researchers to decipher intercellular communications. CellMsg is freely available at https://github.com/pengsl-lab/CellMsg.

Indexed as

Cell CommunicationComputational BiologySoftwareAlgorithmsHumansLigandsSingle-Cell AnalysisLigandscell–cell communicationsgraph convolutional networksligand–receptor interactionsthree-point estimation method

Identifiers

PMID39800874
PMCPMC11725396

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.