ArticleNpj imaging2025
Aptamer-based NIR II imaging for breast cancer surgical resection.
Article in Npj imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.
What it found
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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.
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.
Who cites it
3 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Diagnostic accuracy and surgical outcomes of fluorescence-guided surgery in breast cancer: a systematic review and meta-analysis.World journal of surgical oncology · 2026Pooled it
- A target-activated AS1411 aptamer probe forFrontiers in bioengineering and biotechnology · 2026Article
- Delineating precise surgical resection areas: recent advances in NIR-II fluorescence imaging molecular probes.Frontiers in oncology · 2026Review
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
The accuracy of intraoperative tumor margin assessment is the main challenge in breast conserving surgery (BCS). NIR-II fluorescence-guided surgery enables surgeons to visualize the tumor margins dynamically in real time and facilitate the precision of tumor resection. We develop an aptamer-conjugated NIR-II probe for intraoperative fluorescence imaging. Peglated indocyanine green (PEG-ICG) was conjugated with an aptamer SYL3C binding to EpCAM to synthesize the probe SYL3C-ICG. Human breast cancer cell lines with different expression levels of EpCAM were employed to assess its tumor-targeting capability. Tumor xenograft models were established to investigate the in vivo selectivity of SYL3C-ICG, and a segmental excision procedure was employed to evaluate the efficacy of the probe in navigating precise surgical resection under NIR-II imaging. In vitro and in vivo fluorescence imaging revealed that NIR-II provides superior imaging resolution and penetration depth compared to NIR-I, and SYL3C-ICG could selectively accumulate at the tumor site, which helps surgeons detect tiny residual malignant lesions invisible to the naked eye and reduce the postoperative recurrence rate.
Identifiers
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Registered trials
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.