Evidence map›Paper›PMID 42489176›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Molecular Engineering Boosts Photon-Activated Immunotherapy for Prostate Cancer Through Concurrent Pyroptosis and cGAS-STING Pathway Activation.

Cheng Zhang, Xiaolan Yin, Jeongyeon Hong, Qixian Chen, Weijie Chi, Jingyun Wang, Juyoung Yoon, Haidong Li

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

8 authors.

Cheng ZhangCancer Hospital of Dalian University of Technology, State Key Laboratory of Fine Chemicals, MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, China.
Xiaolan YinCancer Hospital of Dalian University of Technology, State Key Laboratory of Fine Chemicals, MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, China.
Jeongyeon HongDepartment of Chemistry and Nanoscience, Ewha Womans University, Seoul, South Korea.
Qixian ChenInnovation Center of Yangtze River Delta, Zhejiang University, Jiaxing, Zhejiang, China.ORCID https://orcid.org/0000-0002-3091-671X
Weijie ChiSchool of Chemistry and Chemical Engineering, Hainan University, Haikou, China.ORCID https://orcid.org/0000-0003-1776-0025
Jingyun WangCancer Hospital of Dalian University of Technology, State Key Laboratory of Fine Chemicals, MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, China.
Juyoung YoonDepartment of Chemistry and Nanoscience, Ewha Womans University, Seoul, South Korea.ORCID https://orcid.org/0000-0002-1728-3970
Haidong LiCancer Hospital of Dalian University of Technology, State Key Laboratory of Fine Chemicals, MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, China.ORCID https://orcid.org/0000-0002-2721-0337

Funding

Hainan Provincial Natural Science Foundation of China 226JCQN0965Korean government (MSIT) 2022R1A2C3005420LiaoNing Revitalization Talents Program XLYC2503083National Key Research and Development Program of China 2023YFB3810300National Natural Science Foundation of China 22378050National Natural Science Foundation of China 22378051the Ministry of Science and ICT RS-2024-00407093
6 · The paper itself

Abstract

Prostate cancer therapy is often limited by metastasis, drug resistance, and systemic toxicity. Photodynamic immunotherapy (PDIT) offers a promising alternative, yet its efficacy depends on photosensitizers that can simultaneously generate reactive oxygen species (ROS) and activate antitumor immunity. Herein, three thiophene (T) dyes based on triphenylamine (D) and N-ethyl-benzoselenazolium iodide (Se) (DTSe)-based photosensitizers were molecularly engineered by modulating the π-conjugated structure. Incorporation of a carbazole unit affords DZTSe with suppressed fluorescence, enlarged Huang-Rhys factor, reduced singlet-triplet energy gap, and prolonged triplet-state lifetime, resulting in enhanced ROS generation. Notably, DZTSe exhibits multi-organelle localization in the endoplasmic reticulum and mitochondria, concurrently inducing pyroptosis and activating the cGAS-STING pathway. This dual stress-immune activation reprograms the tumor microenvironment and enables effective eradication of primary tumors and suppression of distant lesions in vivo, providing a molecular blueprint for immune-activating photosensitizers.

Indexed as

Antineoplastic AgentsImmunotherapyMembrane ProteinsNucleotidyltransferasesPhotosensitizing AgentsProstatic NeoplasmsPyroptosisAnimalscGAS-STING Signaling PathwayCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseHumansMaleMicePhotochemotherapyPhotonsReactive Oxygen SpeciesAntineoplastic AgentscGAS protein, humanCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseMembrane ProteinsNucleotidyltransferasesPhotosensitizing AgentsReactive Oxygen SpeciesSTING ProteincGAS‐STING pathwayimmune responsephotodynamic immunotherapyprostate cancerpyroptosis pathway

Identifiers

PMID42489176
PMCPMC13592311

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.