Evidence map›Paper›PMID 38611028›Full record

ArticleCancers2024

Identification of Interpretable Clusters and Associated Signatures in Breast Cancer Single-Cell Data: A Topic Modeling Approach.

Gabriele Malagoli, Filippo Valle, Emmanuel Barillot, Michele Caselle, Loredana Martignetti

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Gabriele MalagoliInstitut Curie, Inserm U900, Mines ParisTech, PSL Research University, 75248 Paris, France.ORCID 0000-0002-6386-5031
Filippo VallePhysics Department, University of Turin and INFN, 10125 Turin, Italy.ORCID 0000-0003-3577-8667
Emmanuel BarillotInstitut Curie, Inserm U900, Mines ParisTech, PSL Research University, 75248 Paris, France.ORCID 0000-0003-2724-2002
Michele CasellePhysics Department, University of Turin and INFN, 10125 Turin, Italy.ORCID 0000-0001-5488-142X
Loredana MartignettiInstitut Curie, Inserm U900, Mines ParisTech, PSL Research University, 75248 Paris, France.ORCID 0000-0003-1535-7515
Inserm · FRUniversity of Turin · IT

Funding

European Commission's Horizon 2020 Program, H2020-SC1-DTH-2018-1 826121
6 · The paper itself

Abstract

Topic modeling is a popular technique in machine learning and natural language processing, where a corpus of text documents is classified into themes or topics using word frequency analysis. This approach has proven successful in various biological data analysis applications, such as predicting cancer subtypes with high accuracy and identifying genes, enhancers, and stable cell types simultaneously from sparse single-cell epigenomics data. The advantage of using a topic model is that it not only serves as a clustering algorithm, but it can also explain clustering results by providing word probability distributions over topics. Our study proposes a novel topic modeling approach for clustering single cells and detecting topics (gene signatures) in single-cell datasets that measure multiple omics simultaneously. We applied this approach to examine the transcriptional heterogeneity of luminal and triple-negative breast cancer cells using patient-derived xenograft models with acquired resistance to chemotherapy and targeted therapy. Through this approach, we identified protein-coding genes and long non-coding RNAs (lncRNAs) that group thousands of cells into biologically similar clusters, accurately distinguishing drug-sensitive and -resistant breast cancer types. In comparison to standard state-of-the-art clustering analyses, our approach offers an optimal partitioning of genes into topics and cells into clusters simultaneously, producing easily interpretable clustering outcomes. Additionally, we demonstrate that an integrative clustering approach, which combines the information from mRNAs and lncRNAs treated as disjoint omics layers, enhances the accuracy of cell classification.

Indexed as

breast cancerhierarchical stochastic block modelinglong non-coding RNAssingle-cell RNA-seqtopic modeling

Identifiers

PMID38611028
PMCPMC11011054
OpenAlexW4393357024

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.