Evidence map›Paper›PMID 41889461›Full record

ArticleChemical & biomedical imaging2026

Enzyme-Activated Dual-Locked Probes for Detecting Nitroreductase and Carboxylesterase.

Xiaodan Chong, Zimeng Luo, Junhong Liu, Wenli Jiang, Jinfeng Cen, Yin Gong, Linwen Tan, Zhipeng Pei, Gengxi Jiang, Yuping Zhu and 1 more

Abstract read
In one paragraph

Article in Chemical & biomedical imaging, 2026. 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

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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.

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. Article
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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

11 authors.

Xiaodan ChongClinical Cancer Institute, Translational Medicine Center, Naval Military Medical University, Shanghai 200433, China.
Zimeng LuoFaculty of Naval Medicine, Naval Military Medical University, Shanghai 200433, China.
Junhong LiuFaculty of Naval Medicine, Naval Military Medical University, Shanghai 200433, China.
Wenli JiangBasic Medical College, Naval Military Medical University, Shanghai 200433, China.
Jinfeng CenFaculty of Naval Medicine, Naval Military Medical University, Shanghai 200433, China.
Yin GongFaculty of Naval Medicine, Naval Military Medical University, Shanghai 200433, China.
Linwen TanSchool of Public Health, China Medical University, Shenyang 110122, China.
Zhipeng PeiFaculty of Naval Medicine, Naval Military Medical University, Shanghai 200433, China.
Gengxi JiangDepartment of Thoracic Surgery, Changhai Hospital, Naval Military Medical University, Shanghai 200433, China.
Yuping ZhuBasic Medical College, Naval Military Medical University, Shanghai 200433, China.
Wen-Qi MengFaculty of Naval Medicine, Naval Military Medical University, Shanghai 200433, China.ORCID https://orcid.org/0000-0002-9146-1675

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer, the leading cause of global cancer mortality, demands precise diagnostic tools that target the tumor microenvironment. Hypoxia-driven nitroreductase (NTR) and carboxylesterase (CarE) overexpression serve as promising biomarkers in lung cancer, yet fluorescent probes that can simultaneously detect these markers are not available. Here, we present a series of fluorescein-based probes, with Flu-NitroCa-4 emerging as the optimal dual-locked probe. Flu-NitroCa-4 exhibits a 48-fold fluorescence enhancement at 515 nm upon activation by CarE and NTR, with rapid response kinetics (<30 min) and low detection limits (LOD = 0.18 μg/mL for NTR and 0.032 U/mL for CarE). In vitro, Flu-NitroCa-4 accurately visualizes the activity of CarE and NTR in both A549 cells and patient-derived lung cancer organoids under hypoxic conditions, as validated by inhibitor studies; in vivo, it delineates tumors in subcutaneous and orthotopic murine lung tumors models. Additionally, Flu-NitroCa-4 can be effectively utilized to distinguish human lung cancer samples from adjacent tissues via NTR/CarE-triggered fluorescence. The dual-locked fluorescent probe offers a rapid, low-radiation, and high-sensitivity tool for intraoperative tumor margin mapping and clinical diagnosis.

Indexed as

carboxylesterasefluorescent probehypoxialung cancernitroreductase

Identifiers

PMID41889461
PMCPMC13014316

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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.