Evidence map›Paper›PMID 39780487›Full record

ArticleBriefings in bioinformatics2024

Deciphering progressive lesion areas in breast cancer spatial transcriptomics via TGR-NMF.

Juntao Li, Shan Xiang, Dongqing Wei

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 1 paper.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

3 authors.

Juntao LiSchool of Mathematics and Statistics, Henan Normal University, 46 Jianshe East Road, 453007 Xinxiang, China.ORCID 0000-0002-3288-4395
Shan XiangSchool of Mathematics and Statistics, Henan Normal University, 46 Jianshe East Road, 453007 Xinxiang, China.ORCID 0009-0005-8606-798X
Dongqing WeiSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 800 Dongchuan Road, 200240 Shanghai, China.ORCID 0000-0003-4200-7502

Funding

National Natural Science Foundation of China 61203293Scientific and Technological Project of Henan Province 242102211023
6 · The paper itself

Abstract

Identifying spatial domains is critical for understanding breast cancer tissue heterogeneity and providing insights into tumor progression. However, dropout events introduces computational challenges and the lack of transparency in methods such as graph neural networks limits their interpretability. This study aimed to decipher disease progression-related spatial domains in breast cancer spatial transcriptomics by developing the three graph regularized non-negative matrix factorization (TGR-NMF). A unitization strategy was proposed to mitigate the impact of dropout events on the computational process, enabling utilization of the complete gene expression count data. By integrating one gene expression neighbor topology and two spatial position neighbor topologies, TGR-NMF was developed for constructing an interpretable low-dimensional representation of spatial transcriptomic data. The progressive lesion area that can reveal the progression of breast cancer was uncovered through heterogeneity analysis. Moreover, several related pathogenic genes and signal pathways on this area were identified by using gene enrichment and cell communication analysis.

Indexed as

Breast NeoplasmsTranscriptomeAlgorithmsComputational BiologyDisease ProgressionFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansbreast cancernon-negative matrix factorizationspatial domainspatial transcriptomics

Identifiers

PMID39780487
PMCPMC11711100

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.