Evidence map›Paper›PMID 41334038›Full record

ArticleChemical science2026

AI-enabled new sensing technology: colorimetric analysis of exosomes for precise diagnosis of breast cancer.

Xinyu Qu, Bingqian Lu, Chengge Gao, Weizun Zhao, Yujing Zeng, Shuai Wu, Chenbo Ji, Genxi Li

Abstract read
In one paragraph

Article in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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.

Xinyu QuState Key Laboratory of Analytical Chemistry for Life Science, School of Life Sciences, Nanjing University Nanjing 210023 PR China.
Bingqian LuState Key Laboratory of Analytical Chemistry for Life Science, School of Life Sciences, Nanjing University Nanjing 210023 PR China.
Chengge GaoState Key Laboratory of Analytical Chemistry for Life Science, School of Life Sciences, Nanjing University Nanjing 210023 PR China.
Weizun ZhaoInstitute of AI for Industries Nanjing 211135 PR China.
Yujing ZengCenter for Molecular Recognition and Biosensing, School of Life Sciences, Shanghai University Shanghai 200444 PR China.
Shuai WuClinical Medicine Research Institute, The First Affiliated Hospital with Nanjing Medical University Nanjing 210029 Jiangsu PR China.
Chenbo JiState Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Women and Children's Healthcare Institute, Women's Hospital of Nanjing Medical University, Nanjing Women and Children's Healthcare Hospital, Nanjing Medical University Nanjing 210004 PR China.ORCID https://orcid.org/0000-0002-9869-4228
Genxi LiState Key Laboratory of Analytical Chemistry for Life Science, School of Life Sciences, Nanjing University Nanjing 210023 PR China.ORCID https://orcid.org/0000-0001-9663-9914

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorimetric sensors are widely utilized in biomedical detection owing to their simple operation and intuitive visual results. However, their inherent limitation in the output signal makes sensors insufficient in handling multiple biomarker combination information required for the diagnosis of highly heterogeneous diseases like breast cancer. To overcome the limitation, this study draws inspiration from the mechanism by which the human visual system perceives a myriad of colors using only three cone cell types. So, we propose a novel AI-enabled bionic mixed-color sensing technology for accurate breast cancer subtyping through exosome (EXO) analysis. This technology gives EXO a unique "mixed color fingerprint" by simultaneously binding color-coded nanoprobes (Ab-DyeNPs) targeting different proteins (PD-L1, EpCAM, and HER-2) on the EXO. This mixed-color signal is subsequently recognized by computer vision and analyzed using machine learning algorithms to yield a diagnostic conclusion. For cell line models, this technology accurately differentiates various breast cancer subtypes, reaching up to 100% accuracy. More importantly, it achieved 96.7% accuracy in subtyping clinical samples, outperforming both single-target and multi-target analysis strategies. This study transforms complex multi-dimensional biological information into intuitive visual data, providing a rapid and highly accurate novel tool for precise subtyping of breast cancer, which holds significant potential for clinical application.

Identifiers

PMID41334038
PMCPMC12667402

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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.