Evidence map›Paper›PMID 37370847›Full record

ArticleCancers2023

Identification of Novel Diagnostic and Prognostic Gene Signature Biomarkers for Breast Cancer Using Artificial Intelligence and Machine Learning Assisted Transcriptomics Analysis.

Zeenat Mirza, Md Shahid Ansari, Md Shahid Iqbal, Nesar Ahmad, Nofe Alganmi, Haneen Banjar, Mohammed H Al-Qahtani, Sajjad Karim

Abstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Review
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  6. Article
  7. Article
  8. The role and therapeutic value of NUSAP1 in human cancers.Journal of translational medicine · 2025
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
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  16. Review
  17. An overview of CCN4 (WISP1) role in human diseases.Journal of translational medicine · 2024
    Review
  18. Article
  19. Review
  20. Cancers · 2023
    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

8 authors.

Zeenat MirzaKing Fahd Medical Research Center, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0002-6222-4873
Md Shahid AnsariDepartment of Clinical Data Analytics, Max Super Speciality Hospital, Saket, New Delhi 110017, India.ORCID 0000-0002-7046-7218
Md Shahid IqbalDepartment of Statistics and Computer Applications, Tilka Manjhi Bhagalpur University, Bhagalpur 812007, India.ORCID 0000-0002-9553-6718
Nesar AhmadDepartment of Statistics and Computer Applications, Tilka Manjhi Bhagalpur University, Bhagalpur 812007, India.ORCID 0000-0001-5852-2889
Nofe AlganmiComputer Science Department, Faculty of Computing and Information Technology, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0002-1219-5592
Haneen BanjarComputer Science Department, Faculty of Computing and Information Technology, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0003-4475-4878
Mohammed H Al-QahtaniDepartment of Medical Laboratory Science, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Sajjad KarimDepartment of Medical Laboratory Science, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0003-0907-2097

Funding

King Abdulaziz Hospital IFPRC-125-141-2020
6 · The paper itself

Abstract

backgroundBreast cancer (BC) is one of the most common female cancers. Clinical and histopathological information is collectively used for diagnosis, but is often not precise. We applied machine learning (ML) methods to identify the valuable gene signature model based on differentially expressed genes (DEGs) for BC diagnosis and prognosis.

methodsA cohort of 701 samples from 11 GEO BC microarray datasets was used for the identification of significant DEGs. Seven ML methods, including RFECV-LR, RFECV-SVM, LR-L1, SVC-L1, RF, and Extra-Trees were applied for gene reduction and the construction of a diagnostic model for cancer classification. Kaplan-Meier survival analysis was performed for prognostic signature construction. The potential biomarkers were confirmed via qRT-PCR and validated by another set of ML methods including GBDT, XGBoost, AdaBoost, KNN, and MLP.

resultsWe identified 355 DEGs and predicted BC-associated pathways, including kinetochore metaphase signaling, PTEN, senescence, and phagosome-formation pathways. A hub of 28 DEGs and a novel diagnostic nine-gene signature (

conclusionThe ML approach helped construct novel diagnostic and prognostic models based on the expression profiling of BC. The identified nine-gene signature and eight-gene signatures showed excellent potential in BC diagnosis and prognosis, respectively.

Indexed as

artificial intelligencebreast cancerdiagnostic and prognostic modelgene expression profilingmachine learning methods

Identifiers

PMID37370847
PMCPMC10296674

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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.