Evidence map›Paper›PMID 38816569›Full record

ReviewNPJ precision oncology2024

A review of machine learning methods for cancer characterization from microbiome data.

Marco Teixeira, Francisco Silva, Rui M Ferreira, Tania Pereira, Ceu Figueiredo, Hélder P Oliveira

Abstract readReview
In one paragraph

Review in NPJ precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Programming the tumor microenvironment through microbiome-driven mechanisms.Frontiers in cellular and infection microbiology · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. SIMBA-GNN: mechanistic graph learning for microbiome prediction.NPJ systems biology and applications · 2025
    Article
  10. Advancements in Cancer Survival Prediction: A Systematic Review of Classical and Modern Approaches.Indian journal of community medicine : official publication of Indian Association of Preventive & Social Medicine · 2025
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. The cancer microbiome.Advances in clinical chemistry · 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

6 authors.

Marco TeixeiraInstitute for Systems and Computer Engineering, Technology and Science, Porto, Portugal. marco.a.teixeira@inesctec.pt.ORCID http://orcid.org/0000-0002-7219-0478
Francisco SilvaInstitute for Systems and Computer Engineering, Technology and Science, Porto, Portugal.ORCID http://orcid.org/0000-0003-3069-2282
Rui M FerreiraIpatimup - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.ORCID http://orcid.org/0000-0003-0961-2356
Tania PereiraInstitute for Systems and Computer Engineering, Technology and Science, Porto, Portugal.ORCID http://orcid.org/0000-0003-1681-2436
Ceu FigueiredoIpatimup - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.ORCID http://orcid.org/0000-0001-5247-840X
Hélder P OliveiraInstitute for Systems and Computer Engineering, Technology and Science, Porto, Portugal.ORCID http://orcid.org/0000-0002-6193-8540

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have shown that the microbiome can impact cancer development, progression, and response to therapies suggesting microbiome-based approaches for cancer characterization. As cancer-related signatures are complex and implicate many taxa, their discovery often requires Machine Learning approaches. This review discusses Machine Learning methods for cancer characterization from microbiome data. It focuses on the implications of choices undertaken during sample collection, feature selection and pre-processing. It also discusses ML model selection, guiding how to choose an ML model, and model validation. Finally, it enumerates current limitations and how these may be surpassed. Proposed methods, often based on Random Forests, show promising results, however insufficient for widespread clinical usage. Studies often report conflicting results mainly due to ML models with poor generalizability. We expect that evaluating models with expanded, hold-out datasets, removing technical artifacts, exploring representations of the microbiome other than taxonomical profiles, leveraging advances in deep learning, and developing ML models better adapted to the characteristics of microbiome data will improve the performance and generalizability of models and enable their usage in the clinic.

Identifiers

PMID38816569
PMCPMC11139966

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.