Evidence map›Paper›PMID 42852086›Full record

ReviewFrontiers in molecular biosciences2026

AI-driven multi-omics integration in breast cancer: clinical applications, immunotherapy prediction, and translational challenges.

Zi-Yao Wang, Na Liu, Min-Bin Chen

Abstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Zi-Yao WangDepartment of Radiotherapy and Oncology, Affiliated Kunshan Hospital of Jiangsu University, Kunshan, China.
Na LiuDepartment of Radiotherapy and Oncology, Affiliated Kunshan Hospital of Jiangsu University, Kunshan, China.
Min-Bin ChenDepartment of Radiotherapy and Oncology, Affiliated Kunshan Hospital of Jiangsu University, Kunshan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer remains a major global threat to women's health, and its marked molecular, spatial, and temporal heterogeneity continues to limit the accuracy of early diagnosis, risk stratification, and treatment-response prediction. Conventional single-dimensional diagnostic and therapeutic models are often insufficient to capture the dynamic complexity of the tumor microenvironment (TME). In this context, artificial intelligence (AI) provides powerful tools for high-dimensional feature extraction, multimodal data integration, and cross-scale modeling of heterogeneous biological and clinical information. AI-enabled approaches can link microscopic molecular alterations with macroscopic imaging and pathological phenotypes, while also characterizing complex cellular interactions within the TME. This review summarizes current applications of AI-driven multimodal and multi-omics integration in breast cancer, focusing on early detection, precision diagnosis, immunotherapy-response prediction, drug-sensitivity assessment, and prognostic evaluation. We also discuss key translational challenges, including data heterogeneity, batch effects, interpretability, privacy protection, regulatory considerations, and clinical workflow integration. Overall, AI-driven multi-omics strategies offer a promising framework for improving individualized treatment selection and real-time monitoring in breast cancer, although robust prospective validation and multidisciplinary implementation are still required before routine clinical adoption. Compared with previous modality-specific reviews, this article emphasizes cross-modal evidence appraisal, clinical-maturity stratification, data-quality constraints, foundation model opportunities, and regulatory requirements for translating AI-enabled multi-omics from exploratory research to clinically auditable decision support.

Indexed as

artificial intelligencebreast cancermultimodal datamulti-omicsprecision medicineprognosis

Identifiers

PMID42852086
PMCPMC13647173

What Socratic holds

Textmetadata
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 Socratic graph.