Evidence map›Paper›PMID 41373775›Full record

ArticleInternational journal of molecular sciences2025

Tumor Imaging Heterogeneity Index-Inspired Insights into the Unveiling Tumor Microenvironment of Breast Cancer.

Qingpei Lai, Xinzhi Teng, Jiang Zhang, Xinyu Zhang, Yufeng Jiang, Yao Pu, Peixin Yu, Wen Li, Tian Li, Jing Cai and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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

11 authors.

Qingpei LaiDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
Xinzhi TengDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-7515-8302
Jiang ZhangDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-5807-1686
Xinyu ZhangDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
Yufeng JiangDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
Yao PuDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0009-0004-3133-5054
Peixin YuDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
Wen LiDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0002-9550-3828
Tian LiDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.
Jing CaiDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-6934-0108
Ge RenDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0003-2049-2682

Funding

Guangdong Basic and Applied Basic Research Foundation 2025A1515012926Health and Medical Research Fund 11222456Shenzhen Science and Technology Program JCYJ20230807140403007
6 · The paper itself

Abstract

This study addresses the limited mechanistic understanding behind medical imaging for tumor microenvironment (TME) assessment. We developed a novel framework that analyzes tumor imaging heterogeneity index (TIHI)-correlated genes to uncover underlying TME biology and therapeutic vulnerabilities. DCE-MRI and mRNA data from 987 high-risk breast cancer patients in the I-SPY2 trial, together with mRNA data from 508 patients in GSE25066, were analyzed. TIHI-associated genes were identified via Pearson correlation, clustered via weighted gene co-expression network analysis (WGCNA), and subgroups were defined via non-negative matrix factorization (NMF). The clinical relevance of the image-to-gene comprehensive (I2G-C) subtype defined by subgroups was assessed using logistic regression and Cox analysis. I2G-C comprised four clusters with distinct immune and replication/repair functions. It further stratified receptor, PAM50, and RPS5 subtypes. The "immune+/replication+" was more likely to achieve pathological complete response (pCR) (OR = 2.587,

Indexed as

Breast NeoplasmsTumor MicroenvironmentBiomarkers, TumorFemaleGene Expression Regulation, NeoplasticHumansMagnetic Resonance ImagingBiomarkers, Tumorbreast cancerimage-to-gene comprehensive subtypetumor imaging heterogeneity indextumor microenvironment

Identifiers

PMID41373775
PMCPMC12692328

What OpenQuestion holds

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Registered trials

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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.