Evidence map›Paper›PMID 42639950›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Theranostic Potential of an NAD(P)H-Activatable Fluorophore: Assessing Cancer Aggressiveness and Triggering Apoptosis.

Yujin Cha, Taehoon Oh, Hui Joo Kim, Minju Kang, Shin A Yoon, Yul Lee, Yeon-Ju Lee, Sun Young Park, Dong-Sik Shin, Sung-Kyun Ko and 2 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 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

12 authors.

Yujin Cha *Department of Chemistry, Sookmyung Women's University, Seoul, Republic of Korea.
Taehoon Oh *Chemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju, Republic of Korea.ORCID https://orcid.org/0000-0001-9458-4833
Hui Joo Kim *Department of Chemistry, Chung-Ang University, Seoul, Republic of Korea.
Minju KangDepartment of Chemistry, Chung-Ang University, Seoul, Republic of Korea.
Shin A YoonTherapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology (KRICT), Daejeon, South Korea.
Yul LeeDepartment of Chemical and Biological Engineering, Sookmyung Women's University, Seoul, Republic of Korea.
Yeon-Ju LeeDepartment of Chemical and Biological Engineering, Sookmyung Women's University, Seoul, Republic of Korea.
Sun Young ParkDepartment of Chemistry, Sookmyung Women's University, Seoul, Republic of Korea.
Dong-Sik ShinDepartment of Chemical and Biological Engineering, Sookmyung Women's University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-8101-0793
Sung-Kyun KoChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju, Republic of Korea.ORCID https://orcid.org/0000-0002-8202-1205
Jiyou HanDepartment of Biomedical and Chemical Sciences, Laboratory of Stem Cell Research and Biotechnology, Hyupsung University, Hwaseong-si, Republic of Korea.
Min Hee LeeDepartment of Chemistry, Chung-Ang University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-8061-6371

Funding

Korean National Research Foundation (NRF) 2022-NR070845Korean National Research Foundation (NRF) 2022R1A2C2007696Korean National Research Foundation (NRF) 2024-00440614Korean National Research Foundation (NRF) 2025-16072917Korean National Research Foundation (NRF) 2026-25474382Korea Research Institute of Bioscience and Biotechnology (KRIBB) KGM1272612National Research Council of Science & Technology (NST) CAP23013-300
6 · The paper itself

Abstract

Molecular theranostics, integrating precise diagnosis with targeted therapy, represents a cornerstone of personalized medicine. As a pivotal metabolic cofactor, reduced nicotinamide adenine dinucleotide (phosphate) (NAD(P)H) is intrinsically linked to cancer progression and survival when dysregulated. In this study, we report DE-CQ, an NAD(P)H-activatable fluorophore that enables both cancer imaging and apoptosis. DE-CQ allows the real-time quantification and visualization of intracellular NAD(P)H, serving as a robust molecular indicator of cancer malignancy. Beyond its diagnostic utility, DE-CQ preferentially induces mitochondria- and ER stress-dependent, caspase-mediated apoptosis in aggressive MDA-MB-231 cancer cells while maintaining minimal toxicity toward normal cells. Our findings demonstrate that DE-CQ functions as a potent theranostic agent, simultaneously providing diagnostic insights into cancer aggressiveness and triggering cell death. Given its dual functionality and high selectivity, DE-CQ holds significant potential as a next-generation platform for advanced, personalized cancer treatment.

Indexed as

ApoptosisFluorescent DyesNADPTheranostic NanomedicineCell Line, TumorFluorescent Chemosensor CompoundsHumansMDA-MB-231 CellsOptical ImagingFluorescent Chemosensor CompoundsFluorescent DyesNADPapoptosiscancer aggressivenessfluorescence imagingNAD(P)Htheranostics

Identifiers

PMID42639950
PMCPMC13653622

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.