Evidence map›Paper›PMID 41184341›Full record

ArticleScientific reports2025

Adaptive multi-omics integration framework for breast cancer survival analysis.

Esmaeil Hasanzadeh, Nasrollah Moghadam Charkari

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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.

Esmaeil HasanzadehFaculty of Electrical and Computer Engineering, Tarbiat Modares University, Tehran, Iran.
Nasrollah Moghadam CharkariFaculty of Electrical and Computer Engineering, Tarbiat Modares University, Tehran, Iran. moghadam@modares.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer remains a major global health issue, requiring novel strategies for prognostic evaluation and therapeutic decision-making. In this study, we leverage multi-omics data from The Cancer Genome Atlas to obtain deeper insights into breast cancer biology. By integrating genomics, transcriptomics, and epigenomics, we aim to identify complex molecular signatures that drive breast cancer progression and impact patient survival. To optimize the integration and feature selection process within the multi-omics dataset, we have employed genetic programming. Genetic programming helps us to optimize multi-omics integration, enabling the identification of robust biomarkers and more accurate survival analysis. The proposed framework consists of three key components: data preprocessing, adaptive integration and feature selection via genetic programming, and model development. The experimental results indicate that the integrated multi-omics approach yields a concordance index (C-index) of 78.31 during 5 fold cross-validation on the training set and 67.94 on the test set. In conclusion, our study demonstrates the potential of adaptive multi-omics integration in improving breast cancer survival analysis. It also highlights the importance of considering the complex interplay between different molecular layers. Furthermore, this framework provides a flexible and scalable approach that can be extended to other cancer types, offering valuable insights into oncological processes.

Indexed as

Breast NeoplasmsGenomicsBiomarkers, TumorEpigenomicsFemaleGene Expression ProfilingHumansMultiomicsPrognosisSurvival AnalysisTranscriptomeBiomarkers, TumorBreast cancerData integrationGenetic programmingMulti-omicsSurvival analysis

Identifiers

PMID41184341
PMCPMC12583665

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.