Evidence map›Paper›PMID 39840058›Full record

ArticleFrontiers in immunology2024

Integrating single cell analysis and machine learning methods reveals stem cell-related gene S100A10 as an important target for prediction of liver cancer diagnosis and immunotherapy.

Shenjun Huang, Tingting Tu

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Personalized Stem Cell-Based Regeneration in Spinal Cord Injury Care.International journal of molecular sciences · 2025
    Review
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

2 authors.

Shenjun HuangDepartment of Oncology, Nantong Tumur Hospital (Affiliated Tumur Hospital of Nantong University), Nantong, China.
Tingting TuDepartment of Radiation Oncology, Lianyungang Second People's Hospital (Lianyungang Tumur Hospital), Lianyungang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatocellular carcinoma (LIHC) poses a significant health challenge worldwide, primarily due to late-stage diagnosis and the limited effectiveness of current therapies. Cancer stem cells are known to play a role in tumor development, metastasis, and resistance to treatment. A thorough understanding of genes associated with stem cells is crucial for improving the diagnostic precision of LIHC and for the advancement of effective immunotherapy approaches. Method: This research combines single-cell RNA sequencing with machine learning techniques to identify vital stem cell-associated genes that could act as prognostic biomarkers and therapeutic targets for LIHC. We analyzed various datasets, applying negative matrix factorization alongside machine learning algorithms to reveal gene expression patterns and construct diagnostic models. The XGBoost algorithm was specifically utilized to identify key regulatory genes related to stem cells in LIHC, and the expression levels and prognostic significance of these genes were validated experimentally. Results: Our single-cell analysis identified 16 differential prognostic genes associated with liver cancer stem cells. Cluster analysis and diagnostic models constructed using various machine learning techniques confirmed the significance of these 16 genes in the diagnosis and immunotherapy of LIHC. Notably, the XGBoost algorithm identified S100A10 as the stem cell-related gene most relevant to the prognosis of LIHC patients. Experimental validation further supports S100A10 as a potential prognostic marker for this cancer type. Additionally, S100A10 shows a positive correlation with the stem cell marker POU5F1. Conclusion: The results of this study highlight S100A10 as an essential predictor for liver cancer diagnosis and treatment response, particularly regarding immunotherapy. This research offers valuable insights into the molecular mechanisms underlying LIHC and suggests S100A10 as a promising target for enhancing treatment outcomes in liver cancer patients.

Indexed as

Biomarkers, TumorCarcinoma, HepatocellularLiver NeoplasmsMachine LearningNeoplastic Stem CellsS100 ProteinsSingle-Cell AnalysisGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImmunotherapyPrognosisBiomarkers, TumorS100 Proteinscancer stem cellhepatocellular carcinomamachine learningS100A10single cell analysis

Identifiers

PMID39840058
PMCPMC11747724

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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.